Feasibility of Remote-Delivery Interventions: Tai Chi and Wellness for PTSD and Pain in Veterans

Boston University1 site in 1 country42 target enrollmentJune 22, 2023

ConditionsPTSD Pain, Chronic

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: PTSD
Sponsor: Boston University
Enrollment: 42
Locations: 1
Primary Endpoint: Participant Satisfaction Post Treatment With Interventions Being Tested
Status: Completed
Last Updated: 5 months ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

In the proposed trial, the investigators plan to refine interventions, then conduct a small randomized trial to provide critical information to inform a future large-scale randomized efficacy trial of Tai Chi for Post Traumatic Stress Disorder (PTSD) and chronic pain. Building on the combined experience the proposed study will progress in new directions to:

Adapt, refine, and standardize two 12-week treatment protocols (Tai Chi and a Wellness control condition) for Veterans diagnosed with PTSD and chronic musculoskeletal pain during Phase One. Tai Chi and Wellness interventions will be adapted for delivery via a videoconferencing platform for the population and piloted in a 'dry run'.
Determine the feasibility and acceptability of a remotely delivered randomized trial of these two interventions and the assessment protocols during Phase Two.
Utilize information from this trial to plan and design a large randomized control study evaluating the efficacy of Tai Chi compared to Wellness for improving outcomes for Veterans with PTSD and chronic musculoskeletal pain.

Registry

clinicaltrials.gov

Start Date

June 22, 2023

End Date

March 28, 2025

Last Updated

5 months ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

Boston University

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Veteran status as indicated by self-report
•PTSD Case Definition. Veterans who meet Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) diagnostic criteria according to DSM-5 diagnostic algorithm for current PTSD as assessed on the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) will be eligible for the study. A diagnosis of current PTSD requires: a traumatic stressor (Criterion A) and the requisite number of symptoms at a severity level of 2 or higher in each symptom cluster. Each symptom is rated on a severity scale of 0 (no symptoms) to 4 (extreme), with 2 representing clinically significant and clearly present symptomatology. An individual must endorse at least one reexperiencing (Criterion B) symptom, at least one avoidance (Criterion C) symptom, at least two symptoms of negative alterations in cognition and mood (Criterion D), and at least two hyperarousal (Criterion E) symptoms. In addition, these symptoms must have been present for at least one month (Criterion F) and cause either clinically significant distress or functional impairment (Criterion G).
•Chronic pain as indicated by complaints of musculoskeletal pain in one or more body regions for six months or more.
•Willing to abstain from initiating evidence-based and mindfulness-based psychotherapy for PTSD, pain and related disorders until completion of the study (i.e., prolonged exposure, cognitive processing therapy, cognitive-behavioral treatment for insomnia or pain, acceptance and commitment therapy, dialectical behavior therapy, mindfulness-based stress reduction). Once enrolled, however, if other providers prescribe treatment or if participants require additional intervention (such as to manage a safety or substance abuse condition), treatment will be allowed, and appropriate referrals will be made. Individuals who are currently engaging in short-term (e.g., 12-week protocol) evidence-based treatment will not be eligible until treatment has ended.
•Access to internet and home computer or tablet device that will allow telehealth delivery of intervention.
•Available to attend either intervention group at the times they are scheduled.
•Enrolled and eligible to receive care in Veterans Health Administration (VHA). The investigators will facilitate enrollment for Veterans not currently enrolled but wish to take part in the study.

Exclusion Criteria

•Lacks the capacity to provide consent.
•Diagnosed major medical disorder (e.g., neurological disorder, cancer, chronic infectious disease or liver disease) or has a moderate or severe traumatic brain injury, which could otherwise explain the health symptoms or interfere with their ability to safely engage in Tai Chi exercises.
•Change in psychotropic or pain medication during the past month. This will minimize amount of symptom change due to medication alterations. (Once enrolled, medication changes are nonetheless expected and will be monitored.)
•Regular current Tai Chi, formal mindfulness meditation program, or yoga practice, defined as at least three hours per week for more than three months. (Veterans with prior experience who do not currently engage in regular practice at this level will be eligible.)
•High risk from a mental health perspective e.g., recent psychiatric hospitalization, high risk flag or a note in their VA electronic health record indicating current high-risk factors, entered into a drug or alcohol detoxification or rehabilitation program, or attempted suicide within the previous year as indicated in their VA electronic health record.
•Pregnant or breastfeeding or plans to become pregnant within the year, assessed via self-report. Enrollment of pregnant or breastfeeding participants could potentially complicate outcomes, as new symptoms are likely to arise during the course of the intervention that are attributable to the pregnancy or breastfeeding and not the intervention or symptoms related to PTSD.
•Reports difficulty standing on feet for the majority of a Tai Chi class (approximately 60 minutes).
•Reports that they have been told by a doctor that they should not engage in physical activity unless recommended by a medical team.
•Reports other reason they cannot safely participate in physical activity.
•Concurrent participation in another clinical trial

Outcomes

Primary Outcomes

Participant Satisfaction Post Treatment With Interventions Being Tested

Time Frame: Post-treatment (about 12 weeks)

Assessed by the self-administered Client Satisfaction Questionnaire (CSQ), an 8-item scale with individual responses ranging from 1 to 4. Higher scores are associated with greater satisfaction with the treatment.

Percentage of Participants Satisfaction at Follow-up With Interventions Being Tested

Time Frame: Post-treatment (about 12 weeks)

Percentage of participants that have a mean CSQ item-score of 3 or greater on the 1-4 scale of the 8 original items at post-treatment.

Number of Participants That Attended at Least 70% of the Treatment Sessions

Time Frame: Post-treatment (about 12 weeks)

The number of participants that attended sessions was monitored by study staff.

The Percentage of Participants That Completed All Assessments

Time Frame: Follow-up (about 6 months)

Number of participants that completed all assessments (baseline through follow-up) was monitored by study staff.

Secondary Outcomes

Credibility of Treatment(4 weeks)
Expectancy of Treatment(4 weeks)
Percentage of Participants Who Completed the Weekly Log Sheet(Post treatment (about 12 weeks))