Actively Recruiting
Cognition After OSA Treatment Among Native American People (CATNAP)
Led by Washington State University · Updated on 2026-01-09
140
Participants Needed
1
Research Sites
151 weeks
Total Duration
On this page
Sponsors
W
Washington State University
Lead Sponsor
M
Missouri Breaks Industries Research, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research project will develop and implement a motivational interviewing and electronic messaging intervention to address obstructive sleep apnea (OSA), positive airway pressure (PAP) adherence, and risk of Alzheimer's disease and related dementias in American Indians. The project will work with American Indian Elders, aged 50 years and older, from three Northern Plains Reservations and surrounding communities. A total of 300 American Indian elders with a confirmed OSA diagnosis and prescribed PAP therapy will be randomized to receive usual care consisting of PAP therapy alone (control condition) or usual care plus the culturally informed CATNAP MI component (intervention condition).
CONDITIONS
Official Title
Cognition After OSA Treatment Among Native American People (CATNAP)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 50 years and older
- Self-report as American Indian or Alaskan Native
- Diagnosed with obstructive sleep apnea
- Prescribed positive airway pressure (PAP) therapy and have a PAP device
- Ability to understand written and spoken English
- Ability and willingness to follow all study protocols
You will not qualify if you...
- Living in a household with someone who is enrolled in the study
- Already using PAP device at Medicaid recommended standards
- Cognitive decline causing inability to consent on their own
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Missouri Breaks Industries Research Inc
Eagle Butte, South Dakota, United States, 57625
Actively Recruiting
Research Team
D
Denise Dillard, PhD
CONTACT
M
Madison B Ramos, BA
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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