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Groups for Regaining Our Wellbeing (GROW)

A Non-inferiority Trial of MBSR and CPT for PTSD

Status
Withdrawn
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01971541
Acronym
GROW
Enrollment
0
Registered
2013-10-29
Start date
2014-04-30
Completion date
2017-03-31
Last updated
2014-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Posttraumatic Stress Disorder

Keywords

mindfulness, behavior therapies, cognitive, posttraumatic stress disorder, group therapy

Brief summary

The proposed study is a randomized, controlled trial that will assess whether two group interventions for PTSD - Mindfulness-Based Stress Reduction (MBSR) and Cognitive Processing Therapy-Cognitive only (CPT-C) result in similar improvements in PTSD symptoms and health-related quality of life (QOL). One hundred fifty-two Veterans with PTSD will be randomized to MBSR (n = 76) or CPT-C (n = 76). Comprehensive assessments will take place post-treatment and 3 months later.

Detailed description

The proposed study is a randomized, controlled non-inferiority trial that will assess whether Mindfulness-Based Stress Reduction (MBSR) and Cognitive Processing Therapy-Cognitive only (CPT-C) result in equivalent improvement in both PTSD symptoms and health-related quality of life (QOL). PTSD symptoms will be measured by the Clinician Administered PTSD Scale - CAPS and health-related QOL will be measured by the SF-36V Mental Component Summary Score - MCS. In an exploratory aim, we will also assess whether there is a clinically meaningful response as defined by improvement in both PTSD symptoms and QOL (defined as a reliable change of 12 points on the CAPS and 10 points on the MCS, respectively, according to the reliable change index).7, 8 One hundred fifty-two Veterans with PTSD will be randomized to MBSR (n = 76) or CPT-C (n = 76). Comprehensive assessments will take place post-treatment and 3 months later. Qualitative analysis of brief semi-structured interview data will be used to identify previously unrecognized factors pertaining to participation, adherence and response to treatment, spirituality and religion as treatment moderators, and to identify common themes that may inform treatment retention efforts for both MBSR and CPT-C. In addition, potential moderators of change in PTSD symptoms and QOL for MBSR and CPT-C will be identified.

Interventions

BEHAVIORALMindfulness-Based Stress Reduction

A validated 8-week group program that teaches mindfulness meditation

BEHAVIORALCognitive Processing Therapy

A validated group program of PTSD treatment, which focuses on cognitive processing.

Sponsors

US Department of Veterans Affairs
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Veterans with current DSM-V diagnosis of PTSD

Exclusion criteria

* Current substance use disorder other than alcohol, * Alcohol involvement that poses a safety concern or is associated with inability to follow through on assessments and class attendance as evinced by past month appointment attendance record in CPRS, * Suicidal or homicidal ideation with intent or plan within the past 3 months, * Self harm in the past 3 months, * A psychotic disorder, * Uncontrolled bipolar disorder, * Chart diagnoses of borderline personality disorder or antisocial personality disorder, * In-patient admission for psychiatric reasons within the past month, * Prior participation in MBSR or CPT.

Design outcomes

Primary

MeasureTime frameDescription
PTSD symptoms3 months follow-upClinician-administered PTSD Scale (CAPS)

Secondary

MeasureTime frameDescription
Health-related Quality of Life3 months follow-upSF-36V

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026