Adherence to Chronic Positive Airway Pressure Therapy in Obese Patients With Sleep-disordered Breathing
1 other identifier
observational
300
1 country
1
Brief Summary
To describe the adherence to positive airway pressure therapy among obese adult patients refered to the respiratory center east
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2026
CompletedFirst Submitted
Initial submission to the registry
January 2, 2026
CompletedFirst Posted
Study publicly available on registry
January 23, 2026
CompletedJanuary 23, 2026
January 1, 2026
4.2 years
January 2, 2026
January 15, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Compliance to noninvasive positive airway pressure therapy (nPAP) - 90 days
Use of nPAP a minimum of 4 hours per night for 70% of the time within a consecutive 30-day period within the first 90 days of having the equipment.
0-3 months after start of noninvasive positive airway pressure therapy
Secondary Outcomes (2)
Mortality
1 year
Compliance to noninvasive positive airway pressure therapy (nPAP) - 1 year
Time Frame: 275 to 365 day after start of noninvasive positive airway pressure therapy
Interventions
Use of Positive Airway Pressure Therapy
Eligibility Criteria
Respiratory center east,
You may qualify if:
- years or older
- Body mass index above 30 kg/m2
- Referred to the Respiratory Center East between january 2021 and january 2024
You may not qualify if:
- Neuromuscular disease
- Spinal cord injury
- Craniofacial malformation
- Scoliosis
- Diaphragmatic paresis
- Referred to profylactic secrete management only
- Already in treatment with nPAP with use of nPAP a minimum of 4 hours per night for 70% of the time within a consecutive 30-day period during the last 90 days.
- No medical indication for start of nPAP.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Respiratory Center East, Rigshospitalet
Glostrup Municipality, 2600, Denmark
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Associate professor
Study Record Dates
First Submitted
January 2, 2026
First Posted
January 23, 2026
Study Start
January 1, 2021
Primary Completion
April 1, 2025
Study Completion
January 1, 2026
Last Updated
January 23, 2026
Record last verified: 2026-01