RECRUITING

Cognition After OSA Treatment Among Native American People (CATNAP)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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).

Official Title

Cognition After Obstructive Sleep Apnea (OSA) Treatment Among Native American People (CATNAP)

Quick Facts

Study Start:2024-12-23
Study Completion:2027-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06227572

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 50 years and older
  2. * Self report American Indian or Alaskan Native
  3. * diagnosed with obstructive sleep apnea
  4. * prescribed PAP therapy and have a device
  5. * \*Ability to understand written and spoken English; and
  6. * \*Ability and willingness to follow all study protocols.
  1. * Living in a household with someone who is enrolled in the study
  2. * Already using PAP device at Medicaid recommended standards
  3. * Cognitive decline, unable to consent on their own

Contacts and Locations

Study Contact

Denise Dillard, PhD
CONTACT
206-708-8633
denise.dillard@wsu.edu
Madison B Ramos, BA
CONTACT
madison.ramos@wsu.edu

Study Locations (Sites)

Missouri Breaks Industries Research Inc
Eagle Butte, South Dakota, 57625
United States

Collaborators and Investigators

Sponsor: Washington State University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12-23
Study Completion Date2027-05-31

Study Record Updates

Study Start Date2024-12-23
Study Completion Date2027-05-31

Terms related to this study

Additional Relevant MeSH Terms

  • Obstructive Sleep Apnea
  • Cognitive Change