Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00962403 · ClinicalTrials.gov registry record · NA

Evaluation of a Yoga Intervention for Post-Traumatic Stress Disorder

A NA study, sponsored by Brigham and Women's Hospital.

Completed
Registry status
NA
Development phase
108
Enrollment target

NCT00962403: Completed NA study, sponsored by Brigham and Women's Hospital.

NCT00962403 is a NA study that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 108 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00962403, a NA study, has completed, sponsored by Brigham and Women's Hospital.

COMPLETED
Registry status
NA
Development phase
108 participants
Enrollment target

Study Summary

The main objective of this preliminary randomized controlled clinical trial is to establish efficacy and feasibility of a yoga-based treatment for PTSD in military veterans as compared to a delayed yoga treatment (waitlist control) group. Secondary objectives are to evaluate PTSD characteristics that may also be improved with the treatment and acceptability and compliance with the treatment.

Interventions

  • BEHAVIORAL Yoga treatment

Trial Details

FieldValue
Enrollment Target 108 participants
Start Date 2009-08
Est. Completion 2012-05
Phase NA
Brigham and Women's Hospital

937 total trials

What the finished NCT00962403 record still lists

NCT00962403 is an interventional study that assigns participants to a tested intervention. The registered 108 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Yoga treatment is the first listed.

NCT00962403 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00962403 about?

NCT00962403 is a clinical study titled "Evaluation of a Yoga Intervention for Post-Traumatic Stress Disorder". The main objective of this preliminary randomized controlled clinical trial is to establish efficacy and feasibility of a yoga-based treatment for PTSD in military veterans as compared to a delayed yoga treatment (waitlist control) group. Secondary objectives are to evaluate PTSD characteristics tha...

What is the current status of trial NCT00962403?

This trial is currently completed. It is a NA study. The enrollment target is 108 participants. The study started on 2009-08. Estimated completion is 2012-05.

What interventions are being tested in trial NCT00962403?

The interventions under investigation include: Yoga treatment (BEHAVIORAL).

Who is sponsoring clinical trial NCT00962403?

This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00962403's enrollment target sits among peer trials

108 825th of 2000 higher than 1,171 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02703207 · 108 participants · NA

    Neurocognitive and Health Impact of Sleep Apnea in Elderly Veterans With Comorbid COPD

  • NCT02744677 · 108 participants · NA

    COMPASSION S3 - Evaluation of the SAPIEN 3 Transcatheter Heart Valve in Patients With Pulmonary Valve Dysfunction

  • NCT02781883 · 108 participants · Phase 2

    Clinical Trial of BP1001 in Combination With With Venetoclax Plus Decitabine in AML

  • NCT03848663 · 108 participants · NA

    Visual Remapping to Aid Reading With Field Loss

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00962403, the US trial registry maintained by the National Library of Medicine. NCT00962403 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.