Functional Improvement in OSA and COPD With a Telehealth LifeStyle and Exercise Intervention
NCT06390345
This study is recruiting at 5 US sites in 4 states, according to its ClinicalTrials.gov record last updated .
Summary
The investigators will conduct a Type I hybrid effectiveness-implementation study to test an integrated telehealth intervention among 400 overweight and obese patients with Chronic Obstructive Pulmonary Disease (COPD) and Obstructive Sleep Apnea (OSA). The investigators will include eligible participants receiving primary care at one of five Department of Veterans Affairs (VA) medical centers and their community-based outpatient clinics. The investigators will randomize patients in a 1:1 ratio to the multi-component intervention or "enhanced" usual care, stratifying by age (≥65 vs.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Chronic Obstructive Pulmonary Disease
- Obstructive Sleep Apnea
- Overweight and Obesity
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Seattle Institute for Biomedical and Clinical Research
- Last updated on ClinicalTrials.gov
- July 22, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Idaho · 1
- Boise VA Medical Center · Boise, ID
Illinois · 1
- Jesse Brown VA Medical Center · Chicago, IL
Minnesota · 1
- Minneapolis VA Health Care System · Minneapolis, MN
Washington · 2
- VA Puget Sound Health Care System · Seattle, WA
- Mann-Grandstaff VA Medical Center · Spokane, WA
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.