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Lifestyle Program for Obstructive Sleep Apnea With Severe Obesity

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Mayo Clinic

Status

Completed

Conditions

Obesity
Obstructive Sleep Apnea

Treatments

Behavioral: Home-based pulmonary rehabilitation (PR) system

Study type

Interventional

Funder types

Other
Industry
NIH

Identifiers

NCT05343000
R43HL162131 (U.S. NIH Grant/Contract)
21-011497

Details and patient eligibility

About

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.

Enrollment

17 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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).

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

17 participants in 1 patient group

Severe Comorbid OSA
Experimental group
Description:
Newly-diagnosed severe comorbid obstructive sleep apnea subjects will use technology to facilitate remote health coaching through a home-based pulmonary rehabilitation (PR) system
Treatment:
Behavioral: Home-based pulmonary rehabilitation (PR) system

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Johanna Hoult, MA

Data sourced from clinicaltrials.gov

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