A Pilot Randomized Controlled Trial of Transcendental Meditation as Treatment for Posttraumatic Stress Disorder in Veterans.
Mayer Bellehsen, Valentina Stoycheva, Barry H. Cohen, Sanford Nidich
Journal of Traumatic Stress February 1, 2022 DOI: 10.1002/jts.22665 (opens in new tab) via PubMed
Summary
AI-generated from the abstractTranscendental Meditation (TM) reduces PTSD symptoms more than treatment-as-usual in veterans. In a randomized controlled trial, 40 veterans with PTSD were assigned to either 16 TM sessions over 12 weeks or usual care. After three months, the TM group showed a significantly larger average decrease in clinician-rated PTSD symptoms (11.28 points) compared to the control group (1.62 points). Half of the TM group no longer met PTSD diagnostic criteria, versus 10% in the control group. Self-reported PTSD, depression, anxiety, and sleep difficulties also improved more with TM. No significant differences were found for anger or quality of life. The findings suggest TM is an effective, non-trauma-focused treatment for PTSD.
Study at a glance
| Characteristics | Randomized controlled trial Pilot study Peer reviewed |
|---|---|
| Sample size | 40 |
| Population | Veterans with PTSD |
| Intervention | Transcendental Meditation |
| Duration | 12-week intervention, 3-month follow-up |
| Key finding | Transcendental Meditation significantly reduced PTSD symptoms compared to treatment-as-usual, with 50% of the TM group no longer meeting PTSD diagnostic criteria at 3-month follow-up. |
Abstract
Preliminary studies have demonstrated the efficacy of Transcendental Meditation (TM) for treating posttraumatic stress disorder (PTSD). The present study extended previous research with a pilot trial of TM as a treatment for PTSD via a single-blinded, randomized controlled design. veterans with PTSD (N = 40) were assigned to a TM intervention or treatment-as-usual (TAU) control group. Participants in the TM group engaged in 16 sessions over 12 weeks, primarily in a 60-min group format. Change in PTSD symptoms, measured via the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) was the primary outcome. Secondary outcomes included self-reported PTSD symptoms, depression, anxiety, sleep difficulties, anger, and quality of life (QoL). Assessments were conducted at baseline and 3-month follow-up. Mean CAPS-5 score decreases were significantly larger for participants in the TM group (M = -11.28, 95% CI [-17.35, -5.20]), compared to the TAU group (M = -1.62, 95% CI [-6.77, 3.52]), p = .012, d = -0.84. At posttest, 50.0% of veterans in the TM group no longer met PTSD diagnostic criteria as compared to 10.0% in the TAU group, p = .007. Adjusted mean changes on self-report measures of PTSD symptoms, depression, anxiety, and sleep difficulties indicated significant reductions in the TM group compared to TAU, ds = .80-1.16. There were no significant group differences regarding anger or QoL. These findings demonstrate the efficacy of TM as a treatment for veterans with PTSD and for comorbid symptoms. Combined with other research, they suggest that TM may be a tolerable, non-trauma-focused PTSD treatment.