. Author manuscript; available in PMC: 2010 Apr 1.

Published in final edited form as: J Consult Clin Psychol. 2010 Apr;78(2):169–183. doi: 10.1037/a0018555

The Effect of Mindfulness-Based Therapy on Anxiety and Depression: A Meta-Analytic Review

Stefan G Hofmann ¹, Alice T Sawyer ¹, Ashley A Witt ¹, Diana Oh ¹

PMCID: PMC2848393 NIHMSID: NIHMS162932 PMID: 20350028

Abstract

BACKGROUND

Although mindfulness-based therapy has become a popular treatment, little is known about its efficacy.

OBJECTIVES

To conduct an effect size analysis of this popular intervention for anxiety and mood symptoms in clinical samples.

DATA SOURCES

A literature search was conducted using PubMed, PsycInfo, the Cochrane Library, and manual searches.

REVIEW METHODS

The search identified 39 studies totaling 1,140 participants receiving mindfulness-based therapy for a range of conditions, including cancer, generalized anxiety disorder, depression, and other psychiatric or medical conditions.

RESULTS

Effect size estimates suggest that mindfulness-based therapy was moderately effective for improving anxiety (Hedges’ g = 0.63) and mood symptoms (Hedges’ g = 0.59) from pre to post-treatment in the overall sample. In patients with anxiety and mood disorders, this intervention was associated with effect sizes (Hedges’ g) of 0.97 and 0.95 for improving anxiety and mood symptoms, respectively. These effect sizes were robust, unrelated to publication year or number of treatment sessions, and were maintained over follow-up.

CONCLUSION

These results suggest that mindfulness-based therapy is a promising intervention for treating anxiety and mood problems in clinical populations.

Keywords: Mindfulness, Therapy, Anxiety Disorders, Depression, Efficacy

The Effect of Mindfulness-Based Therapy on Anxiety and Depression: A Meta-Analytic Review

Derived from ancient Buddhist and Yoga practices, mindfulness-based therapy (MBT), which includes mindfulness-based cognitive therapy (MBCT; e.g., Segal, Williams, & Teasdale, 2002) and mindfulness-based stress reduction (MBSR; e.g., Kabat-Zinn, 1982), has become a very popular form of treatment in contemporary psychotherapy (e.g., Baer, 2003; Bishop, 2002; Hayes, 2004; Kabat-Zinn, 1994; Salmon, Lush, Jablonski, & Sephton, 2009). Several of the applications of MBT (such as MBCT) have been designed as relapse prevention strategies rather than to reduce acute symptoms. Other studies have examined MBT as a symptom-focused treatment. The present study is a review of MBT as a therapy to reduce acute symptoms of anxiety and depression.

Mindfulness refers to a process that leads to a mental state characterized by nonjudgmental awareness of the present moment experience, including one's sensations, thoughts, bodily states, consciousness, and the environment, while encouraging openness, curiosity, and acceptance (Bishop et al., 2004; Kabat-Zinn, 2003; Melbourne Academic Mindfulness Interest Group, 2006). Bishop and colleagues (2004) distinguished two components of mindfulness, one that involves self-regulation of attention and one that involves an orientation toward the present moment characterized by curiosity, openness, and acceptance. The basic premise underlying mindfulness practices is that experiencing the present moment nonjudgmentally and openly can effectively counter the effects of stressors, because excessive orientation toward the past or future when dealing with stressors can be related to feelings of depression and anxiety (e.g., Kabat-Zinn, 2003). It is further believed that, by teaching people to respond to stressful situations more reflectively rather than reflexively, MBT can effectively counter experiential avoidance strategies, which are attempts to alter the intensity or frequency of unwanted internal experiences (Hayes, Luoma, Bond, Masuda, & Lillis, 2006). These maladaptive strategies are believed to contribute to the maintenance of many, if not all emotional disorders (Bishop et al., 2004; Hayes, 2004). In addition, the slow and deep breathing involved in mindfulness meditation may alleviate bodily symptoms of distress by balancing sympathetic and parasympathetic responses (Kabat-Zinn, 2003). For example, in the case of MBSR (Kabat-Zinn, 1982), the three key components are sitting meditation, Hatha Yoga, and body scan, which is a sustained mindfulness practice in which attention is sequentially directed throughout the body (Kabat-Zinn, 2003).

A number of reviews have recently been conducted to examine the efficacy of MBT (Baer, 2003; Carmody & Baer, 2009; Grossman, Niemann, Schmidt, & Walach, 2004; Ledesma & Kumano, 2008; Mackenzie, Carlson, & Speca, 2005; Matchim & Armer, 2007; Ott, Norris, & Bauer-Wu, 2006; Praissman, 2008; Smith, Richardson, Hoffman, & Pilkington, 2005; Teixeira, 2008; Toneatto & Nguyen, 2007; Winbush, Gross, & Kreitzer, 2007). In fact, it could be argued that the field has become saturated with qualitative reviews on MBT. These reviews generally suggest that MBT may be beneficial to reduce stress, anxiety, and depression. However, the vast majority of these reviews are qualitative in nature and do not quantify the size of the treatment effect. In contrast, only a few reviews applied meta-analytic methods to quantify the efficacy of this treatment (Baer, 2003; Grossman, Niemann, Schmidt, & Walach, 2004; Ledesma & Kumano, 2008). ¹ One of these reviews focused on MBT for stress reduction in cancer patients (Ledesma & Kumano, 2008), whereas another study examined the efficacy of mindfulness for treating distress associated with general physical or psychosomatic problems, such as chronic pain, coronary artery disease, and fibromyalgia (Grossman et al., 2004). The results of these reviews were encouraging, suggesting that MBSR is moderately effective for reducing distress associated with physical or psychosomatic illnesses. However, both reviews were based on a small number of studies with relatively small sample sizes per study. The two reviews that specifically examined the effects of MBT on mood and anxiety symptoms came to divergent conclusions (Baer, 2003; Toneatto & Nguyen, 2007). Whereas Baer (2003) interpreted the literature as suggesting that MBT may be helpful in treating anxiety and mood disorders, Toneatto and Nguyen (2007) concluded that MBT has no reliable effect for these problems.

In sum, although a very popular treatment, it remains unclear whether MBT is effective for reducing mood and anxiety symptoms. Therefore, the goal of the present study was to provide a quantitative, meta-analytic review of the efficacy of MBT for improving anxiety and mood symptoms in clinical populations. For this purpose, we reviewed treatment studies examining the effects of MBT on anxiety and depression in psychiatric and medical populations.

We tested the hypothesis that MBT is an effective treatment for reducing symptoms of anxiety and depression, especially among patients with anxiety disorders and depression. Furthermore, we expected that MBT reduces symptoms of anxiety and depression in chronic medical conditions, such as cancer, which may be experienced by patients as an effect of their physical condition and potential side-effects of treatments.

Methods

Searching

Studies were identified by searching PubMed, PsycInfo, and the Cochrane Library. Searches were conducted for studies published between the first available year and April 1, 2009 using the search term mindfulness combined with the terms meditation, program, therapy, or intervention and anxi*, depress*, mood, or stress. Additionally, an extensive manual review was conducted of reference lists of relevant studies and review papers extracted from the database searches. Articles determined to be related to the topic of mindfulness were selected for further examination.

Selection

Studies were selected if: (1) they included a mindfulness-based intervention, (2) they included a clinical sample (i.e., participants had a diagnosable psychological or physical/medical disorder); (3) they included adult samples (ages 18-65); (4) the mindfulness program was not coupled with Acceptance and Commitment Therapy or Dialectic Behavior Therapy; (5) included a measure of anxiety and/or mood symptoms at both pre- and post-intervention; and (6) provided sufficient data to perform effect size analyses (i.e., means and standard deviations, t or F values, change scores, frequencies, or probability levels). Studies were excluded if the sample overlapped either partially or completely with the sample of another study meeting inclusion criteria for the meta-analysis. In these cases, we selected for inclusion the study with the larger sample size or more complete data for measures of anxiety and depression symptoms. For studies that provided insufficient data but were otherwise appropriate for the analyses, authors were contacted for supplementary data.

Because the vast majority of studies meeting our criteria employed MBSR, MBCT (Segal et al., 2002), or interventions modeled upon MBSR or MBCT, we excluded studies in which the intervention differed substantially from MBSR and MBCT in length (i.e., two sessions as opposed to the typical eight). Furthermore, we excluded studies in which the MBT was not delivered in person (i.e., audio-taped or internet-delivered interventions).

Validity Assessment

In order to address publication bias, we computed the fail-safe N (Rosenthal, 1991; Rosenthal & Rubin, 1988) using the following formula: $X = \frac{K (K {\overset{‒}{Z}}^{2} - 2.706)}{2.706}$ . In this formula, K is the number of studies in the meta-analysis and Z̄ is the mean Z obtained from the K studies. The effect size can be considered robust if the required number of studies (X) to reduce the overall effect size to a non-significant level exceeds 5K + 10 (Rosenthal, 1991). In addition, we constructed a funnel plot to examine the publication bias. No publication bias results in a funnel plot that is symmetrical around the mean effect size. The Trim and Fill method examines whether negative or positive trials are over or under-represented, accounting for the sample size (i.e., where the missing studies would need to fall to make the plot symmetrical). This information can then be used to re-calculate the effect size estimate.

Data Abstraction

For each study, two of the authors (AAW, ATS) selected psychometrically validated measures of depression and anxiety symptoms. In cases where data from only select subscales of a measure were reported, authors were contacted for anxiety and depression subscale data. Three of the authors (AAW, ATS, DO) extracted numerical data from the studies. Data were extracted to analyze changes from pre to post treatment, pre treatment to follow-up, and intent-to-treat (ITT) with last observation carried forward method.

Study Characteristics

We examined whether the effect sizes varied as a function of study characteristics (type of mindfulness-based therapy, study year, number of treatment sessions, quality of study) and clinical characteristics (disorder targeted by the intervention) by using meta-regression analyses. To investigate the effects of categorical moderator variables, we examined 95% confidence intervals. All analyses were completed manually or by using the software program Comprehensive Meta-Analysis, Version 2 (Borenstein, Hedges, Higgins, & Rothstein, 2005).

Quantitative Data Synthesis

Effect sizes for continuous measures of anxiety and depression were calculated using pre-post treatment differences (within-group) for uncontrolled studies and also for controlled studies using Hedges’g and its 95% confidence interval.² The magnitude of Hedges’ g may be interpreted using Cohen's (1988) convention as small (0.2), medium (0.5), and large (0.8).

The correlation between pre-and post-treatment measures is needed in order to calculate the pre-post effect sizes. This correlation could not be determined from the study reports. Therefore, we followed the recommendation by Rosenthal (1993) and assumed a conservative estimation of r = 0.7. We calculated an average Hedges’ g effect size for studies that included measures of severity of anxiety symptoms and a separate Hedges’ g effect size for measures of depressive symptom severity.

Effect size estimates were pooled across studies in order to obtain a summary statistic. The effect size estimates were calculated using the random-effects model rather than the fixed-effects model because the studies included were not functionally identical (Hedges & Vevea, 1998; Moses, Mosteller, & Buehler, 2002). Effect size estimates for ITT and follow-up data were also calculated in the manner described above.

Assessment of Pre-Treatment Symptom Severity

If symptoms of anxiety or depression are not elevated at baseline, there may be little room for improvement over the course of treatment. In order to assess whether the symptoms of anxiety and depression at pre-treatment were elevated in samples not diagnosed with anxiety or mood disorders (e.g., individuals with cancer, pain or other medical problems), we compared scores on the measures of anxiety and depression used in the relevant studies with cutoff scores that mark an elevated level. Specifically, we calculated 95% confidence intervals for the pre-treatment means on all anxiety and depression measures for which established or suggested clinical cutoff scores are available. If the lower bound of the 95% confidence interval was greater than or equal to the cutoff score, we considered the sample to have an elevated level of anxiety or depression at pre-treatment.

In cases where different cutoff scores were recommended for males and females (e.g., the State-Trait Anxiety Inventory), we chose the higher cutoff score in order to be more conservative. The cutoff scores utilized were as follows: Beck Anxiety Inventory: 10 (Beck & Steer, 1990); Beck Depression Inventory: 10 (Beck, Steer, & Garbin, 1988; Kendall, Hollon, Beck, Hammen, & Ingram, 1987); Beck Depression Inventory-II: 14 (Beck, Steer, & Brown, 1996); Beck Depression Inventory- Short Form: 5 (Beck & Beck, 1972); Center for Epidemiologic Studies Depression Scale: 16 (Boyd, Weissman, Thompson, & Meyer, 1977; Radloff, 1991); Hospital Anxiety and Depression Scale: 8 for each subscale (Zigmond & Snaith, 1983); Profile of Mood States- Anxiety subscale: 16 (Higginson, Fields, Koller, & Tröster, 2001); Profile of Mood States- Depression subscale: 14 (Griffith et al., 2005); Symptom Checklist 90- Revised- Anxiety subscale: 0.75 (Schmitz, Hartkamp, & Frake, 2000); Symptom Checklist 90- Revised- Depression subscale: 0.73 (Schmitz et al., 2000); State-Trait Anxiety Inventory: 40 for each subscale (Leong, Farrell, Helme, & Gibson, 2007).

Results

Trial Flow

Our study selection process is illustrated in Figure 1. Of the 727 articles identified in our initial searches as potentially relevant, 39 studies met our selection criteria and were included in the meta-analysis. The characteristics of the included studies are shown in Table 1. These studies included a total of 1,140 patients who received MBT. The most common disorder studied was cancer (n = 9), followed by generalized anxiety disorder (n = 5), depression (n = 4), chronic fatigue syndrome (n = 3), panic disorder (n = 3), fibromyalgia (n = 3), chronic pain (n = 2), social anxiety disorder (n = 2), attention-deficit hyperactivity disorder (n = 1), arthritis (n = 1), binge eating disorder (n = 1), bipolar disorder (n = 1), diabetes (n = 1), heart disease (n = 1), hypothyroidism (n = 1), insomnia (n = 1), organ transplant (n = 1), stroke (n = 1), and traumatic brain injury (n = 1). Many studies targeted more than one disorder, and thus the sum of the above numbers exceeds the total number of studies included. In addition, one study used a sample of patients meeting criteria for any mood disorder (either current or lifetime), one study included patients with heterogeneous anxiety and mood disorders, and one study used a sample of patients with heterogeneous medical diagnoses. All included studies provided data for continuous measures of anxiety and/or depressive symptom severity at pre and post-treatment.

Flow diagram of study selection process.

Table 1.

Description of Studies

Study	Year	Primary Disorder Targeted by Intervention	Number of Tx Sessions	Mindfulness Intervention (N)	Comparison Condition (N)	Total Sample Size	Anxiety Measures	Depression Measures	Jadad Score
Barnhofer et al.	2009	Depression	8	MBCT (14)	TAU, excluding individual psychotherapy (14)	28		BDI-II	3
Barnhofer et al.					TAU, excluding individual psychotherapy (14)			BSS
Bedard et al. & *Bedard et al.	2003	Traumatic	12	MBSR approach (10)	Dropouts used as controls (3)	13	SCL-90-R anxiety subscale	BDI-II	1
Bedard et al. & *Bedard et al.	2005	brain injury		MBSR approach (10)	Dropouts used as controls (3)		SCL-90-R anxiety subscale	SCL-90-R depression subscale
Bogels et al.	2006	SAD	9	Mindfulness and Task Concentration Training (9)	None	9	FNE		1
							SCS
							SFA
							SPAI social phobia subscale
							SPB
Carlson et al. & *Carlson et al.	2003	Cancer	8 + 3-hr retreat	MBSR (42)	None	42	POMS anxiety subscale	POMS depression subscale	1
	2007
							SOSI anxiety/fear subscale	SOSI depression subscale
Carlson & Garland	2005	Cancer	8 + 3-hr retreat	MBSR (63)	None	63	POMS anxiety subscale	POMS depression subscale	0
							SOSI anxiety/fear subscale	SOSI depression subscale
Craigie et al.	2008	GAD	9	MBCT (20)	None	20	BAI	BDI-II	1
							DASS21 anxiety subscale	DASS21 depression subscale
							PSWQ
Dobkin	2008	Breast cancer	8	MBSR (13)	None	13		CES-D	0
Evans et al.	2008	GAD	8	MBCT (11)	None	11	BAI	BDI-II	1
							POMS anxiety subscale
							PSWQ
*Finucane & Mercer	2006	Depression Anxiety	8	MBCT (11)	None	11	BAI	BDI-II	1
Garland et al.	2007	Cancer	8 + 3-hr retreat	MBSR (60)	Healing though the Creative Arts (44)	104	POMS anxiety subscale	POMS depression subscale	1
					Healing though the Creative Arts (44)		SOSI anxiety/fear subscale	SOSI depression subscale
Grossman	2007	Fibromyalgia	8 + 1-day retreat	MBSR (39)	Educational social support group with relaxation training (13)	52	HADS anxiety subscale	HADS depression subscale	1
							IPR anxiety subscale	IPR depression subscale
Kabat-Zinn et al.	1992	GAD	8 + 1-day retreat	MBSR (22)	None	22	BAI	BDI	1
Kabat-Zinn et al.		PD					HAM-A	HAM-D
							MSCL anxiety subscale
							SCL-90-R anxiety subscale
Kenny & Williams	2007	MDD	8	MBCT (46)	None	46		BDI	1
Kenny & Williams		BPAD (depressed phase)
Kievet-Stijnen et al.	2008	Cancer	8 + 1-day retreat	MBSR (47)	None	47	POMS anxiety subscale	POMS depression subscale	1
Kim et al.	2009	GAD	8	MBCT (24)	Anxiety disorder education program (22)	46	BAI	BDI	1
		PD					HAM-A	HAM-D
							SCL-90-R anxiety subscale	SCL-90-R depression subscale
Kingston et al.	2007	MDD	8	MBCT (6)	TAU (11)	17		BDI	1
Kingston et al.								RS
Koszycki et al.	2007	SAD	8 + 1-day retreat	MBSR (22)	CBGT (18)	40	IPSM	BDI-II	2
Koszycki et al.			8 + 1-day retreat				LSAS
							SIAS
							SPS
Kreitzer et al.	2005	Organ transplant	8	MBSR (19)	None	19	STAI state anxiety subscale	CES-D	1
Kristeller & Hallett	1999	BED	7	Mindfulness meditation training (18)	None	18	BAI	BDI	1
Lee et al.	2007	GAD	8	Meditation-based stress management (21)	Educational program (20)	41	HAM-A	BDI	2
		PD			Educational program (20)		SCL-90-R anxiety subscale	HAM-D
								SCL-90-R depression subscale
							STAI
Lengacher et al.	2009	Breast cancer	6	MBSR (40)	Usual care (42)	82	STAI	CES-D	2
Lush et al.	2009	Fibromyalgia	8	MBSR (24)	None	24	BAI	BDI	1
Moustgaard	2005	Stroke	9	Adapted MBCT (23)	None	23	BAI	BDI-II	1
				Adapted MBCT (23)			HADS anxiety subscale	HADS depression subscale
Pradhan et al.	2007	Arthritis	8	MBSR (31)	Waitlist (32)	63	SCL-90-R anxiety subscale	SCL-90-R depression subscale	3
Ramel et al.	2004	Mood disorders (current or lifetime)	8 + half-day retreat	MBSR (11)	Waitlist (11)	22	STAI	BDI	1
			8 + half-day retreat					DAS
								RSQ rumination subscale
Ree & Craigie	2007	Anxiety, Mood (heterogeneous sample)	8	MBCT (23)	None	23	DASS anxiety subscale	BDI	1
Ree & Craigie		Anxiety, Mood (heterogeneous sample)					DASS anxiety subscale	DASS depression subscale
Reibel et al.	2001	Heterogeneous medical diagnoses	8 + 1-day retreat	MBSR (103)	None	103	SCL-90-R anxiety subscale	SCL-90-R depression subscale	1
Rosenzweig et al.	2007	Diabetes	8 + 1-day retreat	MBSR (11)	None	11	SCL-90-R anxiety subscale	SCL-90-R depression subscale	1
Rosenzweig et al.	2009	Chronic pain	8 + 1-day retreat	MBSR (99)	None	99	SCL-90-R anxiety subscale	SCL-90-R depression subscale	1
Sagula & Rice	2004	Chronic pain	8	Mindfulness meditation program (39)	Waitlist or medical assistance (18)	57	STAI	BDI- Short Form	1
Schulte	2007	Hypothyroidism	8	MBCT (8)	None	8	STAI	BDI-II	1
Sephton et al.	2007	Fibromyalgia	8 + 1-day retreat	MBSR (51)	Waitlist (39)	90		BDI	3
Speca et al. & *Carlson et al.	2000	Cancer	7	MBSR (53)	Waitlist (37)	90	POMS anxiety subscale	POMS depression subscale	3
	2001						POMS anxiety subscale	POMS depression subscale
							SOSI anxiety/fear subscale	SOSI depression subscale
Surawy et al.	2005	Chronic Fatigue Syndrome
Study 1		Chronic Fatigue Syndrome	8	Mindfulness training based on MBSR and MBCT (9)	Waitlist (8)	17	HADS anxiety subscale	HADS depression subscale	2
Study 2			8	Mindfulness training based on MBSR and MBCT (10)	None	10	HADS anxiety subscale	HADS depression subscale	1
Study 3			8	Mindfulness training based on MBSR and MBCT (9)	None	9	HADS anxiety subscale	HADS depression subscale	1
Tacon et al.	2003	Heart disease	8	MBSR (9)	Waitlist (9)	18	STAI state anxiety subscale		2
Tacon et al.	2004	Breast cancer	8	MBSR (27)	None	27	STAI state anxiety subscale		0
Tacon et al.	2005	Breast cancer	8	MBSR (30)	None	30	STAI state anxiety subscale		0
Zylowska et al.	2008	ADHD	8	Mindful Awareness Practices for ADHD (24)	None	24	BAI	BDI	1

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Denotes studies providing follow-up data not included in initial study

Note: ADHD = Attention Deficit Hyperactivity Disorder; BED = Binge Eating Disorder; BPAD = Bipolar Affective Disorder; GAD = Generalized Anxiety Disorder; MDD = Major Depressive Disorder; OCD = Obsessive Compulsive Disorder; PD = Panic Disorder; SAD = Social Anxiety Disorder; MBCT = Mindfulness-Based Cognitive Therapy (Segal et al., 2002); MBSR = Mindfulness-Based Stress Reduction (Kabat-Zinn, 1982); TAU= Treatment as usual; BAI = Beck Anxiety Inventory (Beck & Steer, 1990); BDI = Beck Depression Inventory (Beck, Ward, Mendelson, Mock, & Erbaugh, 1961); BDI-II = Beck Depression Inventory II (Beck, Steer, & Brown, 1996); BDI- Short Form = Beck Depression Inventory- Short Form (Beck & Beck, 1972); BSS = Beck Scale for Suicidal Ideation (Beck & Steer, 1991); CES-D = Center for Epidemiologic Studies Depression Scale (Radloff, 1977); DAS = Dysfunctional Attitudes Scale (Weissman & Beck, 1978); DASS = Depression Anxiety Stress Scales (Lovibond & Lovibond, 1996); DASS21 = Depression Anxiety Stress Scales- Short Form (Lovibond & Lovibond, 1996); FNE = Fear of Negative Evaluation Scale (Leary, 1983); HADS = Hospital Anxiety and Depression Scale (Zigmond & Snaith, 1983); HAM-A = Hamilton Anxiety Rating Scale (Hamilton, 1959); HAM-D = Hamilton Depression Rating Scale (Hamilton, 1960); IPR = Inventory of Pain Regulation (Schermelleh-Engel, 1995); IPSM = Interpersonal Sensitivity Measure (Boyce & Parker, 1989); LSAS = Liebowitz Social Anxiety Scale (Liebowitz, 1987); MSCL = Medical Symptom Checklist (Kabat-Zinn, 1982); POMS = Profile of Mood States (McNair et al., 1971); PSWQ = Penn State Worry Questionnaire (Meyer, Miller, Metzger, & Borkovec, 1990); RS = Rumination Scale (Nolen-Hoeksema & Morrow, 1991); RSQ = Response Style Questionnaire (Nolen-Hoeksema & Morrow, 1991); SCL-90-R = Hopkins Symptom Checklist- Revised (Derogatis, 1983); SCS = Self Consciousness Scale (Fenigstein, Scheier, & Buss, 1975); SFA = Self-Focused Attention Scale (Bögels, Alberts, & de Jong, 1996); SIAS = Social Interaction Scale (Mattick & Clarke, 1988); SOSI = Symptoms of Stress Inventory (Leckie & Thompson, 1979); SPAI = Social Phobia and Anxiety Inventory (Turner, Beidel, Dancu, & Stanley, 1989); SPB = Social Phobic Belief Scale (Voncken, Bögels, & De Vries, 2003); SPS = Social Phobia Scale (Mattick & Clarke, 1988); STAI = State-Trait Anxiety Inventory (Speilberger, Gorsuch, & Lushene, 1970).

Study Characteristics

Using the following modified Jadad criteria (Jadad et al., 1996) to provide a relative index of the quality of included studies, the design of each study was evaluated as follows: (1) the study was described as randomized; (2) participants were adequately randomized; (3) the study was described as double blind; (4) the method of double blinding was appropriate; and (5) a description of drop-outs and withdrawals was provided. One point was assigned for each criterion met for a maximum of 5 points. As shown in Table 1, total Jadad scores for included studies ranged from 0 to 3, with a median of 1 (M = 1.23; SD = 0.77). Two independent ratings of Jadad criteria were performed; inter-rater reliability was r = 0.96. Disagreements were resolved through discussion.

Quantitative Data Synthesis

Pre-post effect size

The average pre-post effect size estimate (Hedges’ g) based on the 39 studies was 0.63 (95% CI: 0.53-0.73, p < .01) for reducing anxiety, and 0.59 (95% CI: 0.51-0.66, p < .01) for reducing depression. The details of these analyses are depicted in Tables 2 and 3.

Table 2.

Effect size analysis of studies examining the efficacy of mindfulness-based therapy on anxiety symptoms in various disorders.

Category	Study	Hedges'g	95% Confidence Interval	p-value
Targeted Disorder			95% Confidence Interval	p-value
Anxiety Disorders
GAD	Craigie et al., 2008	0.69	0.32 – 1.06	<0.01
	Evans et al., 2008	0.89	0.38 – 1.41	0.02
GAD/Panic Disorder	Kabat-Zinn et al., 1992	0.84	0.46 – 1.22	<0.01
	Kim et al., 2009	1.61	1.08 – 2.14	<0.01
	Lee et al., 2007	2.13	1.29 – 2.97	<0.01
SAD	Bogels et al., 2006	0.48	−0.01 – 0.98	0.06
	Koszycki et al., 2007	0.93	0.54 – 1.32	<0.01
Subtotal Anxiety Disorders		0.97	0.73 – 1.22	<0.01
Depression	Ramel et al., 2004	0.12	−0.30 – 0.55	0.70
Pain Disorders
Arthritis	Pradhan et al., 2007	0.21	−0.08 – 0.50	0.15
Chronic Pain	Rosenzweig et al., 2009	0.54	0.37 – 0.70	<0.01
	Sagula & Rice, 2004	0.64	0.38 – 0.91	<0.01
Fibromyalgia	Grossman, 2007	0.55	0.29 – 0.80	<0.01
	Lush et al., 2009	0.24	−0.06 – 0.55	0.12
Subtotal Pain Disorders		0.44	0.22 – 0.67	<0.01
Cancer
Breast Cancer	Lengacher et al., 2009	0.75	0.48 – 1.02	<0.01
	Tacon et al., 2004	1.25	0.87 – 1.64	<0.01
	Tacon et al., 2005	1.19	0.84 – 1.55	<0.01
Breast/ Prostate Cancer	Carlson et al., 2003	0.21	−0.03 – 0.44	0.08
Heterogeneous	Carlson & Garland, 2005	0.51	0.31 – 0.71	<0.01
	Garland et al., 2007	0.50	0.29 – 0.70	<0.01
	Kieviet-Stijnen et al., 2008	0.36	0.13 – 0.58	<0.01
	Speca et al., 2000	0.63	0.41 – 0.86	<0.01
Subtotal Cancer		0.63	0.45 – 0.81	<0.01
Medical Problems
Chronic Fatigue	Surawy et al., 2005 (1)	0.69	0.17 – 1.21	0.01
	Surawy et al., 2005 (2)	1.07	0.50 – 1.64	<0.01
	Surawy et al., 2005 (3)	0.73	0.20 – 1.25	0.01
Diabetes	Rosenzweig et al., 2007	0.28	−0.15 – 0.71	0.21
Heart Disease	Tacon et al., 2003	0.79	0.25 – 1.32	<0.01
Heterogeneous	Reibel et al., 2001	0.53	0.37 – 0.69	<0.01
Hypothyroidism	Schulte, 2007	0.30	−0.20 – 0.80	0.23
Organ Transplant	Kreitzer et al., 2005	0.41	0.06 – 0.76	0.02
Stroke	Moustgaard, 2005	0.98	0.59 – 1.36	<0.01
TBI	Bedard et al., 2003	0.47	0.01 – 0.94	0.05
Subtotal Medical Problems		0.61	0.41 – 0.80	<0.01
Other
ADHD	Zylowska et al., 2008	0.68	0.35 – 1.02	<0.01
Anxiety/ Mood	Ree & Craigie, 2007	0.62	0.28 – 0.95	<0.01
BED	Kristeller & Hallett, 1999	0.63	0.25 – 1.00	<0.01
Overall Total		0.63	0.53 – 0.73	<0.01

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Note. The Table shows effect size estimates (Hedges’ g), the 95% confidence intervals, and the significance test of changes in anxiety symptoms from before to after a mindfulness-based intervention in various psychiatric and medical disorders.

ADHD = Attention Deficit Hyperactivity Disorder; BED = Binge Eating Disorder; GAD = Generalized Anxiety Disorder; SAD = Social Anxiety Disorder; TBI = Traumatic Brain Injury.

Table 3.

Effect size analysis of studies examining the efficacy of mindfulness-based therapy on depressive symptoms in various disorders.

Category	Study	Hedges'g	95% Confidence Interval	p-value
Targeted Disorder			95% Confidence Interval	p-value
Anxiety Disorders
GAD	Craigie et al., 2008	0.75	0.37 – 1.13	<0.01
	Evans et al., 2008	0.56	0.10 – 1.02	0.02
GAD/Panic Disorder	Kabat-Zinn et al., 1992	0.81	0.44 – 1.18	<0.01
	Kim et al., 2009	0.92	0.56 – 1.29	<0.01
	Lee et al., 2007	0.78	0.41 – 1.15	<0.01
SAD	Koszycki et al., 2007	0.62	0.28 – 0.96	<0.01
Subtotal Anxiety Disorders		0.75	0.58 – 0.91	<0.01
Depression	Barnhofer et al., 2009	0.80	0.35 – 1.26	<0.01
	Kingston et al., 2007	1.52	0.67 – 2.36	<0.01
	Kenny & Williams, 2007	1.05	0.77 – 1.32	<0.01
	Ramel et al., 2004	0.63	0.14 – 1.13	0.01
Subtotal Depression		0.95	0.71 – 1.18	<0.01
Pain Disorders
Arthritis	Pradhan et al., 2007	0.48	0.18 – 0.78	<0.01
Chronic Pain	Rosenzweig et al., 2009	0.49	0.33 – 0.65	<0.01
	Sagula & Rice, 2004	0.71	0.45 – 0.98	<0.01
Fibromyalgia	Grossman, 2007	0.50	0.24 – 0.75	<0.01
	Lush et al., 2009	0.47	0.16 – 0.79	<0.01
	Sephton, 2007	0.45	0.23 – 0.67	<0.01
Subtotal Pain Disorders		0.51	0.39 – 0.63	<0.01
Cancer
Breast Cancer	Dobkin et al., 2008	0.58	0.15 – 1.01	0.01
	Lengacher et al., 2009	0.66	0.40 – 0.92	<0.01
Breast/ Prostate Cancer	Carlson et al., 2003	0.15	−0.09 – 0.38	0.22
Heterogeneous	Carlson & Garland, 2005	0.44	0.24 – 0.64	<0.01
	Garland et al., 2007	0.45	0.24 – 0.65	<0.01
	Kieviet-Stijnen et al., 2008	0.30	0.07 – 0.52	0.01
	Speca et al., 2000	0.67	0.44 – 0.90	<0.01
Subtotal Cancer		0.45	0.34 – 0.55	<0.01
Medical Problems
Chronic Fatigue	Surawy et al., 2005 (1)	0.13	−0.33 – 0.59	0.58
	Surawy et al., 2005 (2)	0.25	−0.19 – 0.70	0.26
	Surawy et al., 2005 (3)	0.80	0.26 – 1.35	<0.01
Diabetes	Rosenzweig et al., 2007	0.79	0.30 – 1.29	<0.01
Heterogeneous	Reibel et al., 2001	0.48	0.32 – 0.63	<0.01
Hypothyroidism	Schulte, 2007	0.73	0.18 – 1.28	0.01
Organ Transplant	Kreitzer et al., 2005	0.51	0.15 – 0.87	0.01
Stroke	Moustgaard, 2005	1.01	0.63 – 1.40	<0.01
TBI	Bedard et al., 2003	0.73	0.22 – 1.23	<0.01
Subtotal Medical Problems		0.58	0.47 – 0.70	<0.01
Other
ADHD	Zylowska et al., 2008	0.68	0.35 – 1.02	<0.01
Anxiety/ Mood	Ree & Craigie, 2007	0.62	0.28 – 0.95	<0.01
BED	Kristeller & Hallett, 1999	0.63	0.25 – 1.00	<0.01
Overall Total		0.59	0.51 – 0.66	<0.01

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Note. The Table shows effect size estimates (Hedges’ g), the 95% confidence intervals, and the significance test of changes in depressive symptoms from before to after a mindfulness-based intervention in various psychiatric and medical disorders.

ADHD = Attention Deficit Hyperactivity Disorder; BED = Binge Eating Disorder; GAD = Generalized Anxiety Disorder; SAD = Social Anxiety Disorder; TBI = Traumatic Brain Injury.

Publication bias

The effect size observed for measures of depressive symptom severity for uncontrolled trials and MBT of controlled trials corresponded to a z-value of 21.82, indicating that 4,302 studies with an effect size of zero would be necessary to nullify this result (i.e., for the combined 2-tailed p-value to exceed .05). The fail-safe N for measures of anxiety disorder severity was 4,150 (z-value = 21.74). We also constructed funnel plots, which are depicted in Figures 2 and 3. Using the Trim and Fill method, the number of missing studies that would need to fall to the left of the mean effect size in order to make the plot symmetric was n = 7 studies for the analysis of anxiety measures and n = 10 for the analysis of depression measures. Assuming a random-effects model, the new imputed mean effect size was Hedges’ g = 0.51 (95% CI: .39-.63) for anxiety and Hedges’ g = 0.50 (95% CI: 0.42-.58) for depression. In sum, these analyses suggest that the effect size estimates of the pre-post analyses are unbiased.

Funnel plot of precision by Hedges’ g for depression measures.

Effect sizes of studies with participants showing elevated levels of anxiety or depression

A total of 10 studies used MBT in patients without a clinically defined anxiety or mood disorder, but met our criteria for elevated levels of anxiety at pre-treatment: two studies in cancer populations (Tacon, Caldera, & Ronaghan, 2004; Tacon, Caldera, & Ronaghan, 2005), four studies in populations with pain (Grossman, Tiefenthaler-Gilmer, Raysz, & Kesper, 2007; Lush et al., 2009; Sagula & Rice, 2004; Rosenzweig et al., 2009), three studies in populations with other medical problems (Schulte, 2007; Surawy, Roberts, and Silver, 2005 Studies 1 and 2), and one study using a sample with Binge Eating Disorder (Kristeller & Hallett, 1999). The average pre-post effect size estimate (Hedges’ g) based on these studies was 0.67 (95% CI: 0.47-0.87, p < .01). The fail-safe N was robust at 401 (z-value = 12.55). The average pre-post effect size estimate (Hedges’ g) for the 15 studies that did not have elevated levels of anxiety symptoms at pre-treatment was 0.53 (95% CI: 0.42-0.64, p < .01). This result was also robust (fail-safe N = 774; z-value = 14.21).

A total of 8 studies met our criteria for elevated levels of depressive symptoms at pre-treatment: four studies in populations with pain (Lush et al., 2009; Sagula & Rice, 2004; Sephton et al., 2007; Rosenzweig et al., 2009), two studies in populations with other medical problems (Bedard et al., 2003; Reibel, Greeson, Brainard, & Rosenzweig, 2001), one study using a sample with Binge Eating Disorder (Kristeller & Hallett, 1999), and one study using a sample with ADHD (Zylowska et al., 2008). The average pre-post effect size estimate (Hedges’ g) based on these studies was 0.53 (95% CI: 0.44-0.61, p < .01). The fail-safe N was 296 (z-value = 12.08), indicating that these results are also robust. The average pre-post effect size estimate (Hedges’ g) for the 16 studies that did not have elevated levels of depressive symptoms at pre-treatment was 0.50 (95% CI: 0.39-0.61, p < .01). This result was also robust (fail-safe N = 667; z-value = 12.80).

Controlled effect sizes

Sixteen of the identified studies included a control or comparison group. Eight of these studies compared a MBT to a waitlist control, 3 to treatment-as-usual (TAU), and 5 to an active treatment comparison. Because patients in the waitlist control conditions typically received treatment-as-usual, we pooled together studies employing a waitlist control condition with those employing a TAU control condition. The random-effects analysis of the controlled studies employing a waitlist or TAU comparison condition yielded a mean Hedges’ g effect size of 0.41 (95% CI: 0.23-0.59, z = 4.35, p < .01) for continuous measures of depressive symptom severity, and 0.33 (95% CI: 0.11-0.54, z = 2.97, p < .01) for anxiety symptom severity. The random-effects analysis of the controlled studies employing an active treatment comparison condition yielded a mean Hedges’ g effect size of 0.50 (95% CI: 0.26-0.74, z = 4.06, p < .01) for continuous measures of depressive symptom severity, and 0.81 (95% CI: 0.35-1.27, z = 3.47, p < .01) for anxiety symptom severity. However, the fail-safe Ns for controlled studies for measures of depression and anxiety disorder severity were n = 35 studies (z = 4.31) and n = 11 (z = 3.08) for waitlist controlled and TAU studies, and n = 19 studies (z = 4.21) and n = 42 (z = 5.97) for active treatment controlled studies, respectively. These results suggest that the effect size for anxiety disorder severity for active treatment controlled studies is robust. However, the effect sizes for the controlled studies are unreliable and should be considered preliminary.

Intent-to-Treat Analyses

For the six studies that reported ITT data for continuous measures of anxiety or depression symptom severity, we examined effect sizes for MBT from pre- to post-treatment. Three studies reported ITT data for anxiety measures. The effect size for the pooled data was Hedges’ g = 1.06 (95% CI: 0.29-1.84, p = .007). Six studies reported ITT data for depression measures. The effect size for this pooled data was Hedges’ g = 0.55 (95% CI: 0.43-0.67, p < .001). The fail-safe N for measures of anxiety severity was 42 (z-value = 7.55), indicating that 42 studies with an effect size of zero would be necessary to nullify this result. The fail-safe N for measures of depression severity was 123 (z-value = 9.07). Given the small number of studies for these analyses, these results should be interpreted with caution.

Effects at Follow-Up

To examine long-term outcome, we further conducted an effect size analysis for MBT from pre-treatment to the last available follow-up point. A total of nineteen studies reported follow-up data for measures of anxiety or depression symptoms. The mean length of follow-up was 27 weeks (SD = 32), with a median of 12 weeks. Seventeen studies reported follow-up data for anxiety measures. The effect size for the pooled data was Hedges’ g = 0.60 (95% CI: 0.48-0.71, p < .001). Eighteen studies reported follow-up data for depression measures. The effect size for this pooled data was Hedges’ g = 0.60 (95% CI: 0.48-0.72, p < .001). The fail-safe N for measures of anxiety symptoms at follow-up was 806 (z-value = 13.63), and of depression symptoms at follow-up was 952 (z-value = 14.38), suggesting that both effect size estimates can be considered robust.

Moderator Analyses

In order to explore possible predictors of treatment outcome, we conducted moderator analyses only for the within-subject data from participants receiving a MBT.

Treatment Target

In order to examine whether MBT for patients with anxiety disorders and depression results in greater reductions of symptoms of anxiety and depression than MBT for other patients, we compared effect sizes for continuous measures of anxiety and depression symptoms across the following 4 diagnostic categories: anxiety disorders, mood disorders, cancer, and pain.

MBT showed significant effects for reducing anxiety symptoms in individuals with anxiety disorders (n = 7 studies; Hedges’ g = 0.97, 95% CI: 0.72-1.22, p < .01), followed by individuals with cancer (n = 8 studies; Hedges’ g = 0.64, 95% CI: 0.45-0.82, p < .01), and pain disorders (n = 5 studies; Hedges’ g = 0.44, 95% CI: 0.21-0.68, p < .01). However, the intervention had no significant effect on anxiety symptoms in individuals with depression (n = 1 study; Hedges’ g = 0.12, 95% CI: −0.50-0.74, p = 0.70).

Similarly, MBT was effective for reducing depressive symptoms in individuals with a diagnosis of depression (n = 4 studies; Hedges’ g = 0.95, 95% CI: 0.71-1.18, p < .01), followed by individuals with an anxiety disorder (n = 6 studies; Hedges’ g = 0.75, 95% CI: 0.58-0.92, p < .01), pain (n = 6 studies; Hedges’ g = 0.51, 95% CI: 0.39-0.63, p < .01), and cancer (n = 7 studies; Hedges’ g = 0.45, 95% CI: .34-0.56, p < .01).

Type of mindfulness-based intervention

We compared pre-post effect sizes for MBCT and MBSR on both depression and anxiety symptom severity. Nine studies employing MBCT reported data from measures of depressive symptom severity. The mean effect size for this pooled data was Hedges’ g = 0.85 (95% CI: 0.71-1.00, p < .01). Nineteen studies employing MBSR reported data from measures of depressive symptom severity, and the effect size for the pooled data was Hedges’ g = 0.49 (95% CI: 0.42-0.56, p < .01). Six studies employing MBCT reported data from measures of anxiety symptom severity, and the mean effect size for this pooled data was Hedges’ g = 0.79 (95% CI: 0.45-1.13, p < .001). Twenty studies employing MBSR reported data from measures of anxiety symptom severity, and the effect size for the pooled data was Hedges’ g = 0.55 (95% CI: 0.44-0.66, p < .001). These results suggest that MBCT and MBSR are both effective for reducing anxiety and depression from pre to post-treatment.

Publication year

Hedges’ g was not moderated by publication year for either depression (B = −0.002, SE = 0.011, p = 0.86) or anxiety symptoms (B = 0.00007, SE = 0.015, p = 0.99).

Treatment length

Hedges’ g was not moderated by number of treatment sessions for either depression (B = −0.051, SE = 0.041, p = 0.21) or anxiety symptom severity (B = −0.074, SE = 0.055, p = 0.18).

Study Quality

Jadad score did not moderate Hedges’ g for either depression (B = −0.0017, SE = 0.048, p = 0.96) or anxiety symptoms (B = −0.013, SE = 0.042, p = 0.85).

Discussion

MBT is an increasingly popular form of therapy for anxiety and mood problems. Two earlier reviews on the effects of MBT on symptoms of anxiety and depression came to contradictory conclusions with regards to the efficacy of these interventions (Baer, 2003; Toneatto & Nguyen, 2007). Since the publication of these reviews, a sufficient number of clinical trials have been published that justifies a comprehensive effect size analysis of this promising treatment.

Our review of the literature identified 727 articles, of which we analyzed 39 studies to derive effect size estimates. The results showed that the uncontrolled pre-post effect size estimates were in the moderate range for reducing anxiety symptoms (Hedges’ g = 0.63) and depressive symptoms (Hedges’ g = 0.59). MBT in patients with anxiety disorders and depression was associated with large effect sizes (Hedges’ g) of 0.97 (95% CI: 0.72-1.22) and 0.95 (95% CI: 0.71-1.18) for improving anxiety and depression, respectively.

Among individuals with disorders other than anxiety disorders or depression, but who had elevated levels of symptoms of anxiety and depression, MBT was moderately strong (effect sizes of 0.67 and 0.53, respectively), but not significantly greater than among those with relatively lower pre-treatment levels of anxiety and depression (0.53 and 0.50). These results suggest that MBT improves symptoms of anxiety and depression across a relatively wide range of severity and even when these symptoms are associated with other disorders, such as medical problems. It is possible that MBT is associated with a general reduction in stress, perhaps by encouraging patients to relate differently to their physical symptoms so that when they occur their consequences are less disturbing.

It should be noted that two of the four studies investigating depression focused on patients with chronic or treatment-resistant depression (Barnhofer et al., 2009; Kenny & Williams, 2007), and therefore the effect sizes for these studies might be lower than would otherwise be expected. It should also be noted that the effects of MBT on depression and anxiety in chronic conditions, such as cancer, might be smaller because patients may experience physical symptoms listed on depression or anxiety scales as a result of their physical condition or as potential side-effects of medical treatments. In addition, effect sizes for depression and anxiety symptoms in populations with cancer, pain, or other medical conditions may be smaller than effect sizes in populations with anxiety or mood disorders due to a floor effect: that is, patients with a low level of anxiety or depression at pre-treatment may show a relatively smaller degree of improvement after treatment than those with a high level at pre-treatment.

Earlier quantitative and qualitative reviews that were most closely related to our study include the studies by Baer (2003) and Toneatto and Nguyen (2007). Baer (2003) reported an average pre-post effect size of d = 0.59 based on 15 studies that were weighed by sample size. However, the dependent variables were not restricted to anxiety and depression measures but were based on a range of symptom measures, including measures of stress, pain, memory, and binge eating. Therefore, it is difficult to directly compare the effect size estimates found in our study with those reported by Baer.

In contrast to Baer (2003), Toneatto and Nguyen (2007) focused only on anxiety and depression measures. Although published very recently, this review identified only 15 studies that measured anxiety and depression in patients treated with MBT for a variety of problems, including medical conditions (pain, cancer and heart disease). The study also examined non-clinical populations (i.e., community samples). The authors concluded that MBT does not have reliable effects on anxiety and depression. Our study suggests that this conclusion was premature and unsubstantiated. The authors included only controlled studies, thereby excluding a substantial portion of the MBT research. In addition, it is unclear how many studies were identified, how many were excluded, and for what reasons, because this information was not provided. Furthermore, the authors did not conduct an effect size analysis or apply any other standard meta-analytic procedures. Instead, the conclusion was based solely on a qualitative review of a very small number of studies. Finally, their findings were largely based on patients without anxiety disorders or depression. As our review demonstrated, MBT is most efficacious for reducing symptoms of anxiety and depression in populations with mood or anxiety disorders.

In addition to changes from pre to post, we also examined controlled effect sizes. These effect sizes were smaller but still significant (Hedges’ g = 0.50 and 0.81 for reducing symptoms of depression and anxiety in active treatment controlled studies, and Hedges’ g = 0.41 and 0.32 in waitlist and TAU controlled studies). However, the fail-safe N analysis suggested that, except for measures of anxiety symptom severity in active controlled studies, the results of the controlled effect size analyses were unreliable due to the small number of studies. Similarly, although significant, the ITT effect sizes (Hedges’ g = 1.06 and 0.55 for reducing symptoms of depression and anxiety, respectively) should only be considered preliminary. In contrast, the pre-post effect sizes were robust. A meta-analysis of the effects of psychological placebo conditions in anxiety disorder trials (Smits & Hofmann, 2009) yielded a pre- to post-treatment effect size (Hedges’ g) of 0.45 (95% CI: 0.35-0.46), suggesting that the effect sizes associated with MBT are significantly greater than the placebo effect size.

In general, the observed effect sizes were unrelated to publication year, treatment length, or study quality. Finally, the follow-up data suggested that the effects were maintained at follow-up (with a median follow-up period of 12 weeks). It should be noted that conventional CBT (i.e., without mindfulness procedures) is also quite effective for depression and anxiety disorders (e.g., Butler, Chapman, Forman, & Beck, 2006; Hofmann & Smits, 2008a). In their review of meta-analyses examining the efficacy of conventional CBT for unipolar depression, generalized anxiety disorder, panic disorder with or without agoraphobia, social anxiety disorder, and PTSD, Butler et al. (2006) estimated the effect size to be 0.95 (SD: 0.08). Future studies should directly compare the efficacy, cost-effectiveness, patient (and therapist) preference, treatment acceptability, and attrition of conventional CBT and MBT.

In sum, our findings are encouraging and support the use of MBT for anxiety and depression in clinical populations. This pattern of results suggests that MBT may not be diagnosis-specific, but, instead, may address processes that occur in multiple disorders by changing a range of emotional and evaluative dimensions that underlie general aspects of wellbeing. Therefore, MBT may have general applicability. At the same time, a number of limitations should be noted. Most importantly, the results of this study are limited to the meta-analytic technique and, therefore, are dependent on the study selection criteria, the quality of the included studies, expectancy effects, and statistical assumptions about the true values of the included studies (Henggeler, Schoenwald, Swenson, & Borduin, 2006; Hofmann & Smits, 2008b; Moses et al., 2002; Rief & Hofmann, 2008). In order to limit any possible biases, we adopted a relatively conservative approach. Following the recommendations by Moses et al. (2002) and Hedges and Vevea (1998), we analyzed the effect sizes using a random effect model and quantified the quality of the included studies using modified Jadad criteria, which we considered in our analyses as a possible moderator variable. Because we used modified Jadad criteria, the Jadad scores cannot be directly compared with other meta-analytic studies.

Despite the popularity of MBT, relatively few clinical trials have specifically examined this treatment in anxiety disorders and depression. However, a relatively large number of studies have examined changes in anxiety and depressive symptoms in a range of psychiatric and medical disorders. We decided to examine all available studies that reported changes in anxiety and depressive symptoms during the course of MBT. As a result, the included studies differ in the disorders targeted and also in their methodological quality. However, the Jadad scores did not moderate the effect size estimate. Furthermore, it should be noted that the quality and homogeneity of the studies included in the meta-analysis was considerably better than that of studies used for other recently published meta-analytic reviews of established but poorly validated psychodynamic interventions (Leichsenring & Rabung, 2008; Leichsenring, Rabung, & Leibing, 2004). Moreover, the fail-safe N and funnel plot analyses suggest that the results for uncontrolled pre-post effect sizes are robust and unlikely to be the effect of a publication bias or number of treatment sessions and were maintained over an average 27 week follow-up period (median: 12 weeks).

Perhaps the most important bias of meta-analyses is the expectancy effect. Cotton and Cook (1982) recommended early on that the investigators of meta-analyses explicitly state their personal view with regards to the outcome in order to acknowledge and possibly avoid the expectancy effect. At the outset of our review, we were rather critical toward the efficacy of MBT. We expressed our personal view in an earlier theoretical article (Hofmann & Asmundson, 2008) and were fully prepared to report non-significant or only small effects of MBT. We were surprised to find these effects to be rather robust and strong. Therefore, we believe that the expectancy bias was unlikely to be a significant contributor to the results, which generally support the efficacy of MBT.

In order to avoid other common methodological pitfalls of meta-analyses (e.g., Hofmann & Smits, 2008b), we decided to apply relatively liberal selection criteria by including any studies that used MBT while examining treatment related changes in anxiety and depression. Nevertheless, it is important to interpret the findings in the context of the study criteria, because the average effect size estimate is a direct function of these criteria.

Another limitation was the fact that it was possible to calculate a controlled effect size for only 16 of the 39 trials, and except for measures of anxiety symptom severity in active treatment controlled studies, the effect size estimates were not reliable due to a considerable publication bias. However, the pre-post treatment effects were robust and unlikely to be the result of a psychological placebo because the observed effect size is greater than what would be expected from a psychological placebo (Smits & Hofmann, 2009). Nevertheless, future studies are needed to clearly establish the efficacy of MBT in randomized controlled trials.

Improving the quality of reports of meta-analyses of randomized controlled trails: the QUOROM statement checklist

Heading	Subheading	Descriptor	Reported? (Y/N)	Page number
Title		Identify the report as a meta-analysis [or systematic review] of RCTs	Yes	1
Abstract		Use a structured format²⁷	Yes	2
		Describe
	Objectives	The clinical question explicitly	Yes	2
	Data Sources	The databases (ie, list) and other information sources	Yes	2
	Review Methods	The selection criteria (ie, population, intervention, outcome, and study design); methods for validity assessment, data abstraction, and study characteristics, and quantitative data synthesis in sufficient detail to permit replication	Yes	2
	Results	Characteristics of the RCTs included and excluded; qualitative and quantitative findings (ie, point estimates and confidence intervals); and subgroup analyses	Yes	2
	Conclusion	The main results	Yes	2
		Describe
Introduction		The explicit clinical problem, biological rationale for the intervention, and rationale for review	Yes	5
Methods	Searching	The information sources, in detail²⁸ (eg, databases, registers, personal files, expert informants, agencies, hand-searching), and any restrictions (years considered, publication status,²⁹ language of publication^30,31)	Yes	6
	Selection	The inclusion and exclusion criteria (defining population, intervention, principal outcomes, and study design³²)	Yes	6-7
	Validity assessment	The criteria and process used (eg, masked conditions, quality assessment, and their findings^33–36)	Yes	7
	Data abstraction	The process or processes used (eg, completed independently, in duplicate)³⁵,³⁶	Yes	7-8
	Study characteristics	The type of study design, participants’ characteristics, details of intervention, outcome definitions, &c,³⁷ and how clinical heterogeneity was assessed	Yes	8
	Quantitative data synthesis	The principal measures of effect (eg, relative risk), method of combining results (statistical testing and confidence intervals), handling of missing data; how statistical heterogeneity was assessed;³⁸ a rationale for any a-priori sensitivity and subgroup analyses; and any assessment of publication bias³⁹	Yes	8-10
Results	Trial flow	Provide a meta-analysis profile summarising trial flow (see figure)	Yes	10-11; 55
	Study characteristics	Present descriptive data for each trial (eg, age, sample size, intervention, dose, duration, follow-up period)	Yes	11
	Quantitative data synthesis	Report agreement on the selection and validity assessment; present simple summary results (for each treatment group in each trial, for each primary outcome); present data needed to calculate effect sizes and confidence intervals in intention-to-treat analyses (eg 2×2 tables of counts, means and SDs, proportions)	Yes	11-17
Discussion		Summarise key findings; discuss clinical inferences based on internal and external validity; interpret the results in light of the totality of available evidence; describe potential biases in the review process (eg, publication bias); and suggest a future research agenda	Yes	17-24

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Quality of reporting of meta-analyses

Footnotes

Two additional meta-analyses have examined the efficacy of Acceptance and Commitment Therapy (ACT), which includes mindfulness techniques (Powers, Zum Vörde Sive Vörding, & Emmelkamp, 2009; Öst, 2008). Mindfulness exercises in ACT are firmly rooted in the behavioral analytic model of ACT, which is different from mindfulness-based cognitive-behavioral therapy. Furthermore, mindfulness is a relatively small aspect of ACT when compared to the other treatment components, and the two recently published meta-analyses on ACT are comprehensive and still up to date. Therefore, we did not include ACT in our discussion and analyses and instead followed more closely the general approach by Baer (2003) and Toneatto & Nguyen (2007).

Hedges’ g is a variation of Cohen's d that corrects for biases due to small sample sizes (Hedges & Olkin, 1985). Within-group effect size were calculated using the following formula: $d = (\frac{{\overset{‒}{Y}}_{1} - {\overset{‒}{Y}}_{2}}{S_{D i f f e r e n c e}}) \sqrt{2 (1 - r)}$ , where ${\overset{‒}{Y}}_{1}$ is the pretreatment sample mean, ${\overset{‒}{Y}}_{2}$ is the posttreatment sample mean, S_Difference is the standard deviation of the difference, and r is the correlation between pretreatment and posttreatment scores. Hedges’ g can be computed by multiplying d by correction factor $J (d f) = 1 - \frac{3}{4 d f - 1}$ , where df is the degrees of freedom to estimate the within-group standard deviation.

The controlled effect sizes were computed using the following formula: $g = \frac{{\overset{‒}{Δ}}_{M B T} - {\overset{‒}{Δ}}_{C O N T}}{\sqrt{\frac{(n_{M B T} - 1) S D_{C O N T}^{2} + (n_{C O N T} - 1) S D_{M B T}^{2}}{(n_{t o t a l} - 2)}}} \times (1 - \frac{3}{4 (n_{M B T} + n_{C O N T}) - 9})$ , where $\overset{‒}{Δ}$ is the mean pre- to posttreatment change, SD is the standard deviation of posttreatment scores, n is the sample size, MBT refers to the mindfulness-based therapy condition, and CONT refers to the control condition.

References

Baer R. Mindfulness training as a clinical intervention: A conceptual and empirical review. Clinical Psychology: Science and Practice. 2003;10:125–143. [Google Scholar]
*.Barnhofer T, Crane C, Hargus E, Amarasinghe M, Winder R, Williams JMG. Mindfulness-based cognitive therapy as a treatment for chronic depression: A preliminary study. Behaviour Research and Therapy. 2009;47:366–373. doi: 10.1016/j.brat.2009.01.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
Beck AT, Beck RW. Screening depressed patients in family practice: A rapid technique. Postgraduate Medicine. 1972;52:81–85. doi: 10.1080/00325481.1972.11713319. [DOI] [PubMed] [Google Scholar]
Beck AT, Steer RA. Beck Anxiety Inventory Manual. The Psychological Corporation; San Antonio, TX: 1990. [Google Scholar]
Beck AT, Steer RA. Beck Scale for Suicidal Ideation. The Psychological Corporation; San Antonio, TX: 1991. [Google Scholar]
Beck AT, Steer RA, Brown GK. Beck Depression Inventory-II (BDI-II) The Psychological Corporation, Harcourt Brace; Toronto: 1996. [Google Scholar]
Beck AT, Steer RA, Garbin MG. Psychometric properties of the Beck Depression Inventory: Twenty-five years of evaluation. Clinical Psychology Review. 1988;8(1):77–100. [Google Scholar]
Beck AT, Ward CH, Mendelson M, Mock J, Erbaugh J. An inventory for measuring depression. Archives of General Psychiatry. 1961;4:561–571. doi: 10.1001/archpsyc.1961.01710120031004. [DOI] [PubMed] [Google Scholar]
*.Bedard M, Felteau M, Gibbons C, Klein R. A mindfulness-based intervention to improve quality of life among individuals who sustained traumatic brain injuries: One-year follow-up. The Journal of Cognitive Rehabilitation. 2005;23:8–13. doi: 10.1080/0963828031000090489. [DOI] [PubMed] [Google Scholar]
*.Bedard M, Felteau M, Gibbons C, Klein R, Mazmanian D, Fedyk K, Klein R, Richardson J, Parkinson W, Minthorn-Biggs MB. Pilot evaluation of a mindfulness-based intervention to improve quality of life among individuals who sustained traumatic brain injuries. Disability and Rehabilitation: An International, Multidisciplinary Journal. 2003;25:722–731. doi: 10.1080/0963828031000090489. [DOI] [PubMed] [Google Scholar]
Bishop SR. What do we really know about mindfulness-based stress reduction? Psychosomatic Medicine. 2002;64:71–83. doi: 10.1097/00006842-200201000-00010. [DOI] [PubMed] [Google Scholar]
Bishop M, Lau S, Shapiro L, Carlson ND, Anderson J, Carmody Segal ZV, Abbey S, Speca M, Velting D, Devins G. Mindfulness: A proposed operational definition. Clinical Psychology: Science and Practice. 2004;11:230–241. [Google Scholar]
Bögels SM, Alberts M, de Jong PJ. Self-consciousness, self-focused attention, blushing propensity and fear of blushing. Personality and Individual Differences. 1996;21:573–581. [Google Scholar]
*.Bögels SM, Sijbers GFVM, Voncken M. Mindfulness and task concentration training for social phobia: A pilot study. Journal of Cognitive Psychotherapy. 2006;20:33–44. [Google Scholar]
Borenstein M, Hedges L, Higgins J, Rothstein H. Comprehensive meta-analysis, version 2. Biostat Inc.; Englewood, NJ: 2005. [Google Scholar]
Boyce P, Parker G. Development of a scale to measure interpersonal sensitivity. Australian and New Zealand Journal of Psychiatry. 1989;23:341–351. [PubMed] [Google Scholar]
Boyd JH, Weissman MM, Thompson WD, Meyers JK. Screening for depression in a community sample: Understanding the discrepancies between depression symptom and diagnostic scales. Archives of General Psychiatry. 1982;39(10):1195–1200. doi: 10.1001/archpsyc.1982.04290100059010. [DOI] [PubMed] [Google Scholar]
Butler AC, Chapman JE, Forman EM, Beck AT. The empirical status of cognitive-behavioral therapy: A review of meta-analyses. Clinical Psychology Review. 2006;26:17–31. doi: 10.1016/j.cpr.2005.07.003. [DOI] [PubMed] [Google Scholar]
*.Carlson LE, Garland SN. Impact of mindfulness based stress reduction on sleep, mood, stress, and fatigue symptoms in cancer outpatients. International Journal of Behavioral Medicine. 2005;12:278–285. doi: 10.1207/s15327558ijbm1204_9. [DOI] [PubMed] [Google Scholar]
*.Carlson LE, Speca M, Faris P, Patel KD. One year pre-post intervention follow-up of psychological, immune, endocrine and blood pressure outcomes of mindfulness-based stress reduction (MBSR) in breast and prostate cancer patients. Brain, Behavior, and Immunity. 2007;21:1038–1049. doi: 10.1016/j.bbi.2007.04.002. [DOI] [PubMed] [Google Scholar]
*.Carlson LE, Speca M, Patel K, Goodey E. Mindfulness-based Stress Reduction in relation to quality of life, mood, symptoms of stress, and immune parameters in breast and prostate cancer outpatients. Psychosomatic Medicine. 2003;65:571–581. doi: 10.1097/01.psy.0000074003.35911.41. [DOI] [PubMed] [Google Scholar]
*.Carlson LE, Ursuliak Z, Goodey E, Angen M, Speca M. The effects of a mindfulness meditation-based stress reduction program on mood and symptoms of stress in cancer outpatients: 6-month follow-up. Supportive Care in Cancer. 2001;9:112–123. doi: 10.1007/s005200000206. [DOI] [PubMed] [Google Scholar]
Carmody J, Baer RA. How long does a mindfulness-based stress reduction program need to be? A review of class contact hours and effect sizes for psychological distress. Journal of Clinical Psychology. 2009;65:627–638. doi: 10.1002/jclp.20555. [DOI] [PubMed] [Google Scholar]
Cohen J. Statistical power analysis for the behavioral sciences. 2nd ed. Erlbaum; Hillsdale, NJ: 1988. [Google Scholar]
Cotton JL, Cook MS, et al. Meta-Analyses and the effects f various reward systems: Some different conclusions from Johnson. Psychological Bulletin. 1982;92:176–183. [Google Scholar]
*.Craigie MA, Rees CS, Marsh A. Mindfulness-based cognitive therapy for generalized anxiety disorder: A preliminary evaluation. Behavioural and Cognitive Psychotherapy. 2008;36:553–568. [Google Scholar]
Derogatis LR. The SCL-90-R: Administration, Scoring, and Procedures Manual-II. Clinical Psychometric Research; Baltimore, MD: 1983. [Google Scholar]
*.Dobkin PL. Mindfulness-based stress reduction: What processes are at work? Complementary Therapies in Clinical Practice. 2008;14:8–16. doi: 10.1016/j.ctcp.2007.09.004. [DOI] [PubMed] [Google Scholar]
*.Evans S, Ferrando S, Findler M, Stowell C, Smart C, Haglin D. Mindfulness-based cognitive therapy for generalized anxiety disorder. Journal of Anxiety Disorders. 2008;22:716–721. doi: 10.1016/j.janxdis.2007.07.005. [DOI] [PubMed] [Google Scholar]
Fenigstein A, Scheier MF, Buss AH. Public and private self-consciousness: Assessment and theory. Journal of Consulting and Clinical Psychology. 1975;43:522–527. [Google Scholar]
Finucane A, Mercer S. An exploratory mixed methods study of the acceptability and effectiveness of mindfulness-based cognitive therapy for patients with active depression and anxiety in primary care. BMC Psychiatry. 2006;6:1–14. doi: 10.1186/1471-244X-6-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
*.Garland SN, Carlson LE, Cook S, Lansdell L, Speca M. A non-randomized comparison of mindfulness-based stress reduction and healing arts programs for facilitating post-traumatic growth and spirituality in cancer outpatients. Supportive Care in Cancer. 2007;15:949–961. doi: 10.1007/s00520-007-0280-5. [DOI] [PubMed] [Google Scholar]
Griffith NM, Szaflarski JP, Szaflarski M, Kent GP, Schefft BK, Howe SR, Privitera MD. Measuring depressive symptoms among treatment-resistant seizure disorder patients: POMS Depression scale as an alternative to the BDI-II. Epilepsy & Behavior. 2005;7:266–272. doi: 10.1016/j.yebeh.2005.05.004. [DOI] [PubMed] [Google Scholar]
Grossman P, Niemann L, Schmid S, Walach H. Mindfulness-based stress reduction and health benefits: A meta-analysis. Journal of Psychosomatic Research. 2004;57:35–43. doi: 10.1016/S0022-3999(03)00573-7. [DOI] [PubMed] [Google Scholar]
*.Grossman P, Tiefenthaler-Gilmer U, Raysz A, Kesper U. Mindfulness training as an intervention for fibromyalgia: Evidence of post-intervention and 3-year follow up benefits in well-being. Psychotherapy and Psychosomatics. 2007;76:226–233. doi: 10.1159/000101501. [DOI] [PubMed] [Google Scholar]
Hamilton M. The assessment of anxiety states by rating. British Journal of Medical Psychology. 1959;32:50–55. doi: 10.1111/j.2044-8341.1959.tb00467.x. [DOI] [PubMed] [Google Scholar]
Hamilton M. A rating scale for depression. Journal of Neurology, Neurosurgery, and Psychiatry. 1960;23:56–62. doi: 10.1136/jnnp.23.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
Hayes SC, Luoma JB, Bond FW, Masuda A, Lillis J. Acceptance and commitment therapy: Model, processes and outcomes. Behaviour Research and Therapy. 2006;44:1–25. doi: 10.1016/j.brat.2005.06.006. [DOI] [PubMed] [Google Scholar]
Hayes SC. Acceptance and commitment therapy, relational frame theory, and the third wave of behavior therapy. Behavior Therapy. 2004;35:639–665. doi: 10.1016/j.beth.2016.11.006. [DOI] [PubMed] [Google Scholar]
Hedges LV, Olkin I. Statistical methods for meta-analysis. Academic Press; New York, NY: 1985. [Google Scholar]
Hedges LV, Vevea JL. Fixed- and random-effects models in meta-analysis. Psychological Methods. 1998;3:486–504. [Google Scholar]
Henggeler SW, Schoenwald SK, Swenson CC, Borduin CM. Methodological critique and meta-analysis as Trojan horse. Children and Youth Services Review. 2006;20:447–457. [Google Scholar]
Higginson CI, Fields JA, Koller WC, Tröster AI. Questionnaire assessment potentially overestimates anxiety in Parkinson's Disease. Journal of Clinical Psychology in Medical Settings. 2001;8:95–99. [Google Scholar]
Hofmann SG, Asmundson GJ. Acceptance and mindfulness-based therapy: New wave or old hat? Clinical Psychology Review. 2008;28:1–16. doi: 10.1016/j.cpr.2007.09.003. [DOI] [PubMed] [Google Scholar]
Hofmann SG, Smits JAJ. Cognitive-Behavioral Therapy for adult anxiety disorders: A meta-analysis of randomized placebo-controlled trials. Journal of Clinical Psychiatry. 2008a;69:621–632. doi: 10.4088/jcp.v69n0415. [DOI] [PMC free article] [PubMed] [Google Scholar]
Hofmann SG, Smits JAJ. Pitfalls of meta-analyses. Journal of Nervous and Mental Disease. 2008b;196:716–717. doi: 10.1097/NMD.0b013e318183fd90. [DOI] [PubMed] [Google Scholar]
Jadad AR, Moore RA, Carroll D, Jenkinson C, Reynolds DJM, Gavaghan DJ, McQuay HJ. Assessing the quality of reports of randomized clinical trials: Is blinding necessary? Control Clinical Trials. 1996;17:1–12. doi: 10.1016/0197-2456(95)00134-4. [DOI] [PubMed] [Google Scholar]
Kabat-Zinn J. An outpatient program in behavioral medicine for chronic pain patients based on the practice of mindfulness meditation: Theoretical considerations and preliminary results. General Hospital Psychiatry. 1982;4:33–47. doi: 10.1016/0163-8343(82)90026-3. [DOI] [PubMed] [Google Scholar]
Kabat-Zinn J. Wherever you go there you are. Hyperion; New York: 1994. [Google Scholar]
Kabat-Zinn J. Mindfulness-based interventions in context: Past, present, and future. Clinical Psychology: Science and Practice. 2003;10:144–156. [Google Scholar]
*.Kabat-Zinn J, Massion AO, Kristeller J, Peterson LG. Effectiveness of a meditation-based stress reduction program in the treatment of anxiety disorders. American Journal of Psychiatry. 1992;149:936–943. doi: 10.1176/ajp.149.7.936. [DOI] [PubMed] [Google Scholar]
Kendall PC, Hollon SD, Beck AT, Hammen CL, Ingram RE. Issues and recommendations regarding use of the Beck Depression Inventory. Cognitive Therapy and Research. 1987;11:289–299. [Google Scholar]
*.Kenny MA, Williams JMG. Treatment-resistant depressed patients show a good response to Mindfulness-based Cognitive Therapy. Behaviour Research and Therapy. 2007;45:617–625. doi: 10.1016/j.brat.2006.04.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
*.Kieviet-Stijnen A, Visser A, Garssen B, Hudig W. Mindfulness-based stress reduction training for oncology patients: Patients’ appraisal and changes in well-being. Patient Education and Counseling. 2008;72:436–442. doi: 10.1016/j.pec.2008.05.015. [DOI] [PubMed] [Google Scholar]
*.Kim YW, Lee SH, Choi TK, Suh SY, Kim B, Kim CM, Cho SJ, Kim MJ, Yook K, Ryu M, Song SK, Yook KH. Effectiveness of mindfulness-based cognitive therapy as an adjuvant to pharmacotherapy in patients with panic disorder or generalized anxiety disorder. Depression and Anxiety. 2009;26:601–606. doi: 10.1002/da.20552. [DOI] [PubMed] [Google Scholar]
*.Kingston T, Dooley B, Bates A, Lawlor E, Malone K. Mindfulness-based cognitive therapy for residual depressive symptoms. Psychology and Psychotherapy: Theory, Research and Practice. 2007;80:193–203. doi: 10.1348/147608306X116016. [DOI] [PubMed] [Google Scholar]
*.Koszycki D, Benger M, Shlik J, Bradwejn J. Randomized trial of a meditation-based stress reduction program and cognitive behavior therapy in generalized social anxiety disorder. Behaviour Research and Therapy. 2007;45:2518–2526. doi: 10.1016/j.brat.2007.04.011. [DOI] [PubMed] [Google Scholar]
*.Kreitzer MJ, Gross CR, Ye X, Russas V, Treesak C. Longitudinal impact of mindfulness meditation on illness burden in solid-organ transplant recipients. Progress in Transplantation. 2005;15:166–172. doi: 10.1177/152692480501500210. [DOI] [PubMed] [Google Scholar]
*.Kristeller JL, Hallett CB. An exploratory study of a meditation-based intervention for binge eating disorder. Journal of Health Psychology. 1999;4:357–363. doi: 10.1177/135910539900400305. [DOI] [PubMed] [Google Scholar]
Leary MR. A brief version of the Fear of Negative Evaluation Scale. Personality and Social Psychology Bulletin. 1983;9:371–375. [Google Scholar]
Leckie MS, Thompson E. Symptoms of Stress Inventory. University of Washington Press; Seattle, WA: 1979. [Google Scholar]
Ledesma D, Kumano H. Mindfulness-based stress reduction and cancer: A meta-analysis. Psycho-Oncology. 2008;18:571–579. doi: 10.1002/pon.1400. [DOI] [PubMed] [Google Scholar]
*.Lee SH, Ahn SC, Lee YJ, Choi TK, Yook KH, Suh SY. Effectiveness of a meditation-based stress management program as an adjunct to pharmacotherapy in patients with anxiety disorder. Journal of Psychosomatic Research. 2007;62:189–95. doi: 10.1016/j.jpsychores.2006.09.009. [DOI] [PubMed] [Google Scholar]
Leichsenring F, Rabung S. Effectiveness of long-term psychodynamic psychotherapy: A meta-analysis. Journal of the American Medical Association. 2008;300:1551–1565. doi: 10.1001/jama.300.13.1551. [DOI] [PubMed] [Google Scholar]
Leichsenring F, Rabung S, Leibing E. The efficacy of short-term psychodynamic psychotherapy in specific psychiatric disorders: A meta-analysis. Archives of General Psychiatry. 2004;61:1208–1216. doi: 10.1001/archpsyc.61.12.1208. [DOI] [PubMed] [Google Scholar]
*.Lengacher CA, Johnson-Mallard V, Post-White J, Moscoso MS, Jacobsen PB, Klein TW, Widen RH, Fitzgerald SG, Shelton MM, Barta M, Goodman M, Cox CE, Kip KE. Randomized controlled trial of mindfulness-based stress reduction (MBSR) for survivors of breast cancer. Psycho-Oncology. doi: 10.1002/pon.1529. in press. [DOI] [PubMed] [Google Scholar]
Leong IY, Farrell MJ, Helme RD, Gibson SJ. The relationship between medical comorbidity and self-rated pain, mood disturbance, and function in older people with chronic pain. Journal of Gerontology. 2007;62A(5):550–555. doi: 10.1093/gerona/62.5.550. [DOI] [PubMed] [Google Scholar]
Liebowitz MR. Social phobia. Modern Problems of Pharmacopsychiatry. 1987;22:141–173. doi: 10.1159/000414022. [DOI] [PubMed] [Google Scholar]
Lovibond SH, Lovibond PF. Manual for the Depression Anxiety Stress Scales. 2nd ed. Psychology Foundation; Sydney: 1995. [Google Scholar]
*.Lush E, Salmon P, Floyd A, Studts JL, Weissbecker I, Sephton SE. Mindfulness meditation for symptom reduction in fibromyalgia: Psychophysiological correlates. Journal of Clinical Psychology in Medical Settings. 2009;16:200–207. doi: 10.1007/s10880-009-9153-z. [DOI] [PubMed] [Google Scholar]
Mackenzie MJ, Carlson LE, Speca M. Mindfulness-Based Stress Reduction (MBSR) in oncology: Rationale and review. Evidence-based Integrative Medicine. 2005;2:139–145. [Google Scholar]
Matchim Y, Armer JM. Measuring the psychological impact of mindfulness meditation on health among patients with cancer: A literature review. Oncology Nursing Forum. 2007;34:1059–1066. doi: 10.1188/07.ONF.1059-1066. [DOI] [PubMed] [Google Scholar]
Mattick RP, Clarke JC. Development and validation of measures of social phobia scrutiny fear and social interaction anxiety. Behaviour Research and Therapy. 1988;36:455–470. doi: 10.1016/s0005-7967(97)10031-6. [DOI] [PubMed] [Google Scholar]
McNair DM, Lorr M, Droppleman LF. Manual: Profile of Mood States. Educational and Industrial Testing Service; San Diego: 1971. [Google Scholar]
Melbourne Academic Mindfulness Interest Group Mindfulness-based psychotherapies: A review of conceptual foundations, empirical evidence and practical considerations. Australian and New Zealand Journal of Psychiatry. 2006;40:285–294. doi: 10.1080/j.1440-1614.2006.01794.x. [DOI] [PubMed] [Google Scholar]
Meyer TJ, Miller ML, Metzger RL, Borkovec TD. Development and validation of the Penn State Worry Questionnaire. Behaviour Research and Therapy. 1990;28:487–495. doi: 10.1016/0005-7967(90)90135-6. [DOI] [PubMed] [Google Scholar]
Moses LE, Mosteller F, Buehler JH. Comparing results of large clinical trials to those of meta-analyses. Statistics in Medicine. 2002;21:793–800. doi: 10.1002/sim.1098. [DOI] [PubMed] [Google Scholar]
*.Moustgaard A. Mindfulness-Based Cognitive Therapy (MBCT) for stroke survivors: An application of a novel intervention. 2005. Unpublished dissertation.
Nolen-Hoeksema S, Morrow JA. A prospective study of depression and posttraumatic stress symptoms after a natural disaster: The 1989 Loma Prieta earthquake. Journal of Personality & Social Psychology. 1991;61:115–121. doi: 10.1037//0022-3514.61.1.115. [DOI] [PubMed] [Google Scholar]
Öst L-G. Efficacy of the third wave of behavioral therapies: A systematic review of meta-analysis. Behaviour Research and Therapy. 2008;46:296–321. doi: 10.1016/j.brat.2007.12.005. [DOI] [PubMed] [Google Scholar]
Ott MJ, Norris RL, Bauer-Wu SM. Mindfulness meditation for oncology patients: A discussion and critical review. Integrative Cancer Therapies. 2006;5:98–108. doi: 10.1177/1534735406288083. [DOI] [PubMed] [Google Scholar]
Powers MB, Zum Vörde Sive Vörding MB, Emmelkamp PM. Acceptance and commitment therapy: A meta-analytic review. Psychotherapy and Psychosomatics. 2009;78:73–80. doi: 10.1159/000190790. [DOI] [PubMed] [Google Scholar]
*.Pradhan EK, Baumgarten M, Langenberg P, Handwerger B, Gilpin AK, Magyari T, Hochberg MC, Berman BM. Effect of Mindfulness-Based Stress Reduction in rheumatoid arthritis patients. Arthritis and Rheumatism. 2007;57:1134–42. doi: 10.1002/art.23010. [DOI] [PubMed] [Google Scholar]
Praissman S. Mindfulness-based stress reduction: A literature review and clinicians’ guide. Journal of the American Academy of Nurse Practitioners. 2008;20:212–216. doi: 10.1111/j.1745-7599.2008.00306.x. [DOI] [PubMed] [Google Scholar]
Radloff LS. The CES-D scale: A self-report depression scale for research in the general population. Applied Psychological Measurement. 1977;1:385–401. [Google Scholar]
Radloff LS. The use of the Center for Epidemiologic Studies Depression Scale in adolescents and young adults. Journal of Youth and Adolescence. 1991;20:149–166. doi: 10.1007/BF01537606. [DOI] [PubMed] [Google Scholar]
*.Ramel W, Goldin PR, Carmona PE, McQuaid JR. The effects of mindfulness meditation on cognitive processes and affect in patients with past depression. Cognitive Therapy and Research. 2004;28:433–455. [Google Scholar]
*.Ree MJ, Craigie MA. Outcomes following mindfulness-based cognitive therapy in a heterogeneous sample of adult outpatients. Behaviour Change. 2007;24:70–86. [Google Scholar]
*.Reibel DK, Greeson JM, Brainard GC, Rosenzweig S. Mindfulness-based stress reduction and health-related quality of life in a heterogeneous patient population. General Hospital Psychiatry. 2001;23:183–192. doi: 10.1016/s0163-8343(01)00149-9. [DOI] [PubMed] [Google Scholar]
Rief W, Hofmann SG. The missing data problem in meta-analyses. Archives of General Psychiatry. 2008;65:238. doi: 10.1001/archgenpsychiatry.2007.31. [DOI] [PubMed] [Google Scholar]
Rosenthal R. Meta-analytic procedures for social research. rev. ed Sage Publications Inc.; Thousand Oaks, CA: 1991. [Google Scholar]
Rosenthal R. Meta-analytic procedures for social research. Sage Publications; Newbury Park, CA: 1993. [Google Scholar]
Rosenthal R, Rubin DB. Comment: Assumptions and procedures in the file drawer problem. Statistical Science. 1988;3:120–125. [Google Scholar]
*.Rosenzweig S, Greeson JM, Reibel DK, Green JS, Jasser SA, Beasley D. Mindfulness-based stress reduction for chronic pain conditions: Variation in treatment outcomes and role of home meditation practice. Journal of Psychosomatic Research. doi: 10.1016/j.jpsychores.2009.03.010. in press. [DOI] [PubMed] [Google Scholar]
*.Rosenzweig S, Reibel DK, Greeson JM, Edman JS, Jasser SA, McMearty KD, Goldstein BJ. Mindfulness-based stress reduction is associated with improved glycemic control in type 2 diabetes mellitus: A pilot study. Alternative Therapies in Health and Medicine. 2007;13(5):36–38. [PubMed] [Google Scholar]
*.Sagula D, Rice KG. The effectiveness of mindfulness training on the grieving process and emotional well-being of chronic pain patients. Journal of Clinical Psychology in Medical Settings. 2004;11:333–342. [Google Scholar]
Salmon P, Lush E, Jablonski M, Sephton SE. Yoga and mindfulness: Clinical aspects of an ancient mind/body practice. Cognitive and Behavioral Practice. 2009;16:59–72. [Google Scholar]
Schermelleh-Engel K. Handanweisung. Swets; Frankfurt: 1995. Fragebogen zur Schmerzregulation (FSR). [Google Scholar]
Schmitz N, Hartkamp N, Franke GH. Assessing clinically significant change: Application to the SCL-90-R. Psychological Reports. 2000;86:263–274. doi: 10.2466/pr0.2000.86.1.263. [DOI] [PubMed] [Google Scholar]
*.Schulte CF. Effects of mindfulness-based cognitive therapy on the psychological and behavioral symptoms of hypothyroidism. 2007. Unpublished dissertation.
Segal ZV, Williams JMG, Teasdale JD. Mindfulness-Based Cognitive Therapy for Depression: A New Approach to Preventing Relapse. Guilford Press; New York: 2002. [Google Scholar]
*.Sephton SE, Salmon P, Weissbecker I, Ulmer C, Floyd A, Hoover K, Studts JL. Mindfulness meditation alleviates depressive symptoms in women with fibromyalgia: Results of a randomized clinical trial. Arthritis Rheumatoid. 2007;57:77–85. doi: 10.1002/art.22478. [DOI] [PubMed] [Google Scholar]
Smith JE, Richardson J, Hoffman C, Pilkington K. Mindfulness-Based Stress Reduction as supportive therapy in cancer care: Systematic review. Journal of Advanced Nursing. 2005;52:315–327. doi: 10.1111/j.1365-2648.2005.03592.x. [DOI] [PubMed] [Google Scholar]
Smits AJ, Hofmann SG. A meta-analytic review of the effects of psychotherapy control conditions for anxiety disorders. Psychological Medicine. 2009;39:229–239. doi: 10.1017/S0033291708003498. [DOI] [PubMed] [Google Scholar]
*.Speca M, Carlson LE, Goodey E, Angen M. A randomized wait-list controlled clinical trial: The effect of a mindfulness meditation-based stress reduction program on mood and symptoms of stress in cancer outpatients. Psychosomatic Medicine. 2000;62:613–622. doi: 10.1097/00006842-200009000-00004. [DOI] [PubMed] [Google Scholar]
Speilberger CD, Gorsuch RL, Lushene RE. STAI Manual. Consulting Psychologist Press; Palo Alto, CA: 1970. [Google Scholar]
*.Surawy C, Roberts J, Silver A. The effect of mindfulness training on mood and measures of fatigue, activity, and quality of life in patients with Chronic Fatigue Syndrome on a hospital waiting list: A series of exploratory studies. Behavioural and Cognitive Psychotherapy. 2005;33:103–109. [Google Scholar]
*.Tacon AM, Caldera YM, Ronaghan C. Mindfulness-Based Stress Reduction in women with breast cancer. Families, Systems, & Health. 2004;22:193–203. [Google Scholar]
*.Tacon AM, Caldera YM, Ronaghan C. Mindfulness, Psychosocial Factors, and Breast Cancer. Journal of Cancer Pain and Symptom Palliation. 2005;1:45–53. [Google Scholar]
*.Tacon A, McComb JJ, Randolph P, Caldera Y. Mindfulness meditation, anxiety reduction, and heart disease: A pilot study. Family Community Health. 2003;26:25–33. doi: 10.1097/00003727-200301000-00004. [DOI] [PubMed] [Google Scholar]
Teixeira ME. Meditation as an intervention for chronic pain: An integrative review. Holistic Nurse Practitioner. 2008;22:225–234. doi: 10.1097/01.HNP.0000326006.65310.a7. [DOI] [PubMed] [Google Scholar]
Toneatto T, Nguyen L. Does mindfulness meditation improve anxiety and mood symptoms? A review of the controlled research. La Revue Canadienne de Psychiatrie. 2007;52:260–266. doi: 10.1177/070674370705200409. [DOI] [PubMed] [Google Scholar]
Turner SM, Beidel DC, Dancu CV, Stanley MA. An empirically derived instrument to measure social fears and anxiety: The Social Phobia and Anxiety Inventory. Psychological Assessment: A Journal of Consulting and Clinical Psychology. 1989;1:35–40. [Google Scholar]
Voncken M, Bögels SM, De Vries K. Interpretation and judgmental biases in social phobia. Behaviour Research and Therapy. 2003;41:1481–1488. doi: 10.1016/s0005-7967(03)00143-8. [DOI] [PubMed] [Google Scholar]
Weissman AN, Beck AT. Development and validation of the Dysfunctional Attitude Scale: A preliminary investigation.. Paper presented at the meeting of the Association for the Advancement of Behavior Therapy; Chicago. 1978. [Google Scholar]
Winbush NY, Gross CR, Kreitzer MJ. The effects of mindfulness-based stress reduction on sleep disturbance: A systematic review. Explore: The Journal of Science and Healing. 2007;3:585–591. doi: 10.1016/j.explore.2007.08.003. [DOI] [PubMed] [Google Scholar]
Zigmond AS, Snaith RP. The hospital anxiety and depression scale. Acta Psychiatrica Scandinavica. 1983;67:361–370. doi: 10.1111/j.1600-0447.1983.tb09716.x. [DOI] [PubMed] [Google Scholar]
*.Zylowska L, Ackerman DL, Yang MH, Futrell JL, Horton NL, Hale TS, Pataki C, Smalley SL. Mindfulness meditation training in adults and adolescents with ADHD: A feasibility study. Journal of Attention Disorders. 2008;11:737–746. doi: 10.1177/1087054707308502. [DOI] [PubMed] [Google Scholar]

PERMALINK

The Effect of Mindfulness-Based Therapy on Anxiety and Depression: A Meta-Analytic Review

Stefan G Hofmann

Alice T Sawyer

Ashley A Witt

Diana Oh

Abstract

BACKGROUND

OBJECTIVES

DATA SOURCES

REVIEW METHODS

RESULTS

CONCLUSION

The Effect of Mindfulness-Based Therapy on Anxiety and Depression: A Meta-Analytic Review

Methods

Searching

Selection

Validity Assessment

Data Abstraction

Study Characteristics

Quantitative Data Synthesis

Assessment of Pre-Treatment Symptom Severity

Results

Trial Flow

Figure 1.

Table 1.

Study Characteristics

Quantitative Data Synthesis

Pre-post effect size

Table 2.

Table 3.

Publication bias

Figure 2.

Figure 3.

Effect sizes of studies with participants showing elevated levels of anxiety or depression

Controlled effect sizes

Intent-to-Treat Analyses

Effects at Follow-Up

Moderator Analyses

Treatment Target

Type of mindfulness-based intervention

Publication year

Treatment length

Study Quality

Discussion

Footnotes

References

ACTIONS

PERMALINK

RESOURCES

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