Behavioral Optimization to Overcome Obstructive Sleep Apnea Treatment Barriers

Part of paid clinical trials in West Los Angeles, California.

Sponsor
VA Office of Research and Development
Study ID
NCT07207473
Status
Not Yet Recruiting

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Conditions

Eligibility Criteria

Sex
ALL
Age
50 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Behavioral strategy program X plus Y — BEHAVIORAL
    Brief 4 session education program with sleep specialist focused on behavioral strategies for improving use of sleep apnea therapy. Tests behavioral strategy program X plus Y.
  • Behavioral strategy program X — BEHAVIORAL
    Brief 4 session education program with sleep specialist focused on behavioral strategies for improving use of sleep apnea therapy Tests behavioral strategy X.

Study Details

Previous studies have shown that programs encouraging the use of OSA treatments can help patients use these treatments more often, but the improvement is usually modest. This trial will test if giving patients a decision-making tool when they are first diagnosed with OSA, and combining their responses from this tool into a supportive program, will improve sleep quality and help them use their treatment more regularly.

Key Dates

Start date
Nov 2, 2026
Status verified
Jun 2026
Primary completion
Sep 30, 2030
Completion
Mar 31, 2031

Study Design

Enrollment
128 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Sleep education program X + Y
    Brief 4 session education program with sleep specialist focused on behavioral strategies for improving use of sleep apnea therapy. Tests behavioral strategy program X plus Y.
  • Active Comparator: Sleep education program X
    Brief 4 session education program with sleep specialist focused on behavioral strategies for improving use of sleep apnea therapy Tests behavioral strategy X.

Primary Outcome Measure

Pittsburgh Sleep Quality Index (PSQI) [ Time Frame: 6-months after the end of the intervention/control sessions, which is approximately 8 months after randomization. ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
VA Greater Los Angeles Healthcare System, West Los Angeles, CAWest Los AngelesCalifornia90073-1003
Constance H Fung, MD MSHS
[email protected]
(818) 891-7711
Constance H Fung, MD MSHS (PRINCIPAL_INVESTIGATOR)
John D. Dingell VA Medical Center, Detroit, MIDetroitMichigan48201-1916
M. Safwan Badr, MD
[email protected]
313-576-1000
Susmita Chowdhuri, MD
[email protected]
3135761000

Find similar trials in West Los Angeles, CA

By research site
VA Greater Los Angeles Healthcare System, West Los Angeles, CA· West Los Angeles, CAJohn D. Dingell VA Medical Center, Detroit, MI· Detroit, MI

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