Actively Recruiting
Enhancing PAP Adherence Among Spanish-speaking Hispanic Adults With OSA
Led by Geisinger Clinic · Updated on 2024-02-09
50
Participants Needed
4
Research Sites
136 weeks
Total Duration
On this page
Sponsors
G
Geisinger Clinic
Lead Sponsor
A
American Academy of Sleep Medicine
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study seeks to enhance long-term positive airway pressure (PAP) adherence among Spanish-speaking Hispanics, a group with known PAP outcomes disparities. This study will assess the feasibility of a linguistically and culturally adapted tele-management intervention (Automated Management, AM) for Spanish-speaking Hispanic adults with OSA.
CONDITIONS
Official Title
Enhancing PAP Adherence Among Spanish-speaking Hispanic Adults With OSA
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Spanish-speaking and reading
- Self-identified Hispanic
- Adults 18 years or older
- Males and females
- Moderate-severe OSA defined as AHI ≥15 events/hour using 4% oxygen desaturation criterion
- Expected availability for the 6-month study duration
- Ownership of smartphone with unlimited text messaging capability
- Referred to PAP treatment and able and willing to be treated with PAP
You will not qualify if you...
- Diagnosis of other sleep apnea or nocturnal respiratory failure besides OSA
- Requirement of supplemental oxygen or other non-invasive ventilation
- Women referred to PAP due to new pregnancy (except those already on PAP who become pregnant during trial)
- Anticipated or scheduled bariatric surgery or referred to sleep evaluation by bariatric surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
Kaiser Permanent Southern California
Fontana, California, United States, 92335
Actively Recruiting
2
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
3
Geisinger
Danville, Pennsylvania, United States, 17821
Actively Recruiting
4
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
B
Bruno Saconi, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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