The Effect of Interval Exercise on Functional Outcomes in Veterans With COPD and OSA
Part of paid clinical trials in Salem, Virginia.
- Sponsor
- VA Office of Research and Development
- Study ID
- NCT05254431
- Status
- Recruiting
Conditions
- COPD
- OSA
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Exercise — BEHAVIORALNovel Moderate Intensity Interval Exercise The Experimental Design is a randomized trial of moderate intensity interval training (5-minute intervals at 50% VO2peak 3 times weekly for 12 weeks) in Veterans with COPD and OSA compared with standard of care controls
Study Details
The term "Overlap Syndrome" (OS) is used to describe the presence of both chronic obstructive pulmonary disease (COPD) and obstructive sleep apnea (OSA) in a single patient. Due to premature aging, patients with OS are prone to developing functional decline up to 20 years earlier than the general population. The International Classification of Functioning, Disability and Health (ICF) evaluates functional status in chronic pulmonary disease globally in 5 domains. The investigators propose to study validated outcomes in 3 of these domains: 1) participation in life situations; 2) physical activity; and 3) cardiovascular health. The investigators long-term goal is to develop an exercise strategy tailored to Veterans with OS which will reduce the risk of functional decline through increased PA.
Key Dates
- Start date
- Apr 1, 2022
- Status verified
- Apr 2026
- Primary completion
- Apr 1, 2027
- Completion
- Apr 1, 2027
Study Design
- Enrollment
- 28 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: ExerciseThe Experimental Design is a randomized trial of Moderate intensity interval training (5-minute intervals at 50% VO2peak 3 times weekly for 12 weeks) in Veterans with COPD and OSA compared with standard of care controls
- No Intervention: Usual CareParticipants in the control group will be instructed to maintain their routine activity level for 12 weeks
Primary Outcome Measure
Scale number on Epworth Sleepiness Scale [ Time Frame: 12 weeks ]
Central Contacts
- Madalina Macrea, MD PhD
- Kimberly L Birkett, MPH BS(540) 982-2463
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Salem VA Medical Center, Salem, VA | Salem | Virginia | 24153-6404 | Madalina Macrea, MD PhD (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Salem, VA
Related Studies
- Global Utilization And Registry Database for Improved preservAtion of doNor LUNGsEnrolling By Invitation · Paragonix Technologies · Phoenix, Arizona
- A Study to Evaluate Solrikitug in Participants With COPD (ZION)PHASE2 · Recruiting · Uniquity One (UNI) · Birmingham, Alabama
- Continuation Protocol for Obstructive Sleep Apnea (OSA)PHASE3 · Enrolling By Invitation · Apnimed · Birmingham, Alabama
- Respiratory Oxygen Adherence Monitor for Chronic Obstructive Pulmonary Disease PatientsNot Yet Recruiting · Barron Associates, Inc. · Charlottesville, Virginia