N/A
N=54
Exercise and PTSD in Older Veterans
Post-traumatic
Bottom Line
View on ClinicalTrials.gov: NCT02295995 ↗Enrolled (actual)
54
Serious AEs
0.0%
Results posted
Jan 2020
Primary outcome: Primary: Feasibility of Patient Recruitment — 54 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Exercise as an Adjuvant Therapy for Veterans with PTSD (Behavioral)
- Age
- Adult, Older Adult · 60+ yrs
- Sex
- All
- Sponsor
- VA Office of Research and Development
- Primary completion
- May 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Feasibility of Patient Recruitment |
54 | — |
| PRIMARY Physical Activity |
365.8; 349.4; 1954.4; 675.3 | — |
| PRIMARY PTSD Symptoms |
42.97; 41.06; 35.87; 38.19 | — |
| SECONDARY Aerobic Endurance |
462.1; 465.9; 531.1; 476.0 | — |
Summary
The purpose of this study is to examine whether posttraumatic stress disorder (PTSD) symptoms impact adherence to a 12-week physical activity program and whether exercise can help improve PTSD symptoms and health outcomes in older Veterans. Veterans over the age of 60 with PTSD were be recruited to participate in a 12-week physical activity program consisting of aerobic and strengthening activities. 54 participants were randomized to an intervention arm (n=36) or usual care wait-list control (n=18).
Eligibility Criteria
Inclusion Criteria
- Meet diagnostic criteria for current PTSD,
- live within 50 miles of Durham VA Medical Center (VAMC) and have reliable transportation,
- registered for care at the Durham VAMC,
- independently mobile (assistive devices acceptable),
- speak and write fluent conversational English
Exclusion Criteria
- Active substance dependence other than nicotine,
- cognitive impairment, uncontrolled psychotic symptoms,
- clinical history of cardiovascular disease (CVD) occurring within the past 3 months,
- uncontrolled hypertension,
- renal disease or currently receiving dialysis,
- psychotropic medication initiated within 6 weeks prior to enrollment
- proliferative retinopathy
Data sourced from ClinicalTrials.gov (NCT02295995). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.