N/A
N=17
Lifestyle Program for Obstructive Sleep Apnea With Severe Obesity
Obstructive Sleep Apnea · Obesity
Bottom Line
View on ClinicalTrials.gov: NCT05343000 ↗Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcome: Primary: Ability to Use the Devices at Home — 15 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Home-based pulmonary rehabilitation (PR) system (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Mayo Clinic
- Primary completion
- Sep 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Ability to Use the Devices at Home |
15 | — |
| PRIMARY Usability of Proposed System in Patients With OSA and Obesity |
9.5 | — |
| PRIMARY Helpfulness of Set-up Instructions of Proposed System in Patients With OSA and Obesity |
9.2 | — |
| SECONDARY Participant Reported Confidence Using Proposed System in Patients With OSA and Obesity |
15 | — |
| SECONDARY Perceived Benefit of Proposed System in Patients With OSA and Obesity |
15 | — |
Summary
The purpose of this study is to develop a data driven system for persons with severe obesity sleep apnea that utilizes remote monitoring with health coaching to create behavior changes aimed at improving health and quality of life.
Eligibility Criteria
Inclusion Criteria
- Adult patients, 18 years of age or older.
- Diagnosis of Obstructive Sleep Apnea (OSA) and obesity (BMI > or = to 35).
Exclusion Criteria
- Individuals < 18 years of age.
- Patients with an inability to provide good data or follow commands (patients who are disoriented, have a severe neurologic or psychiatric condition).
Data sourced from ClinicalTrials.gov (NCT05343000). 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.