This study is not yet accepting patients

Integrated Health Care for PTSD

a study on Post-Traumatic Stress Disorder Meditation

Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSD
Dates
study started
study ends around

Description

Summary

The goal of this clinical trial is to determine whether which types of integrative care, meaning a combination of psychotherapy and mind-body interventions, lead to the most changes in functioning among Veterans with posttraumatic stress disorder (PTSD). The main aims are:

  1. To evaluate the impact of integrative care approaches on functional outcomes among Veterans with PTSD.
  2. To examine factors relevant to the implementation of integrated treatments for PTSD from the perspective of patients, providers and administrators in the VA Healthcare System.

Participants will:

  1. Complete assessments at the beginning of the study and 12- and 24-weeks later.
  2. Engage in 12 weeks of integrated care, with the type being randomly assigned.

Official Title

A Hybrid I Evaluation of Integrative Health Care for PTSD

Keywords

Posttraumatic Stress Disorder (PTSD), PTSD, complementary and integrative health, Veterans, implementation, Post-Traumatic Stress Disorders, Yoga, Meditation, Health, Yoga and meditation, Wellness, Positive affect, Information

Eligibility

You can join if…

Open to people ages 18 years and up

(1) clinical diagnosis, (2) eligibility for Cognitive Processing Therapy (CPT) at a participating VA site, and (3) able to consent to study activities

You CAN'T join if...

(1) current, active engagement in one of the included approaches (per clinician judgment) or (2) medical conditions that contraindicate engaging in the experimental interventions

Locations

  • VA San Diego Healthcare System
    San Diego 5391811 California 5332921 92161 United States
  • VA Phoenix Healthcare System
    Phoenix 5308655 Arizona 5551752 85012-1839 United States

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
Veterans Medical Research Foundation
ID
NCT07220681
Study Type
Interventional
Participants
Expecting 300 study participants
Last Updated