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Personalized Sleep Apnea Treatment for Black Adults

This study is looking at how well a personalized approach, called PRAISE, helps Black adults with obstructive sleep apnea (OSA) stick to their recommended treatment plan (Positive Airway Pressure or PAP). Participants will be aged 60-85 and have an OSA diagnosis. You would either receive standard sleep apnea care or standard care plus weekly short videos (Personalized OSA Treatment) accessed online. The main goal is to see how many participants in each group follow their OSA treatment over six months. The study aims to enroll 330 people.

Study design
This interventional study plans to enroll 330 participants who will be divided into two groups: one receiving standard care and another receiving standard care plus personalized video treatment.
What's involved
Participants will receive either standard of care for sleep apnea or standard care plus weekly three-minute videos accessed through a web-based application.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint for adherence to OSA treatment is measured up to 6 months.

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NCT06089161

Personalized Obstructive Sleep Apnea Treatment and Effects on Alzheimer's Disease Biomarkers and Cognition Among Blacks

Recruiting
NAAges 60–85InterventionalHealth services
University of Miami
~330 participants
Updated 2025-05-08 on ClinicalTrials.gov
What's tested:Standard of CarePersonalized OSA Treatment

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Proportion of participants adherence to OSA treatment
Measured over Up to 6 months

Conditions

Sleep Apnea

Explore related trials

Obstructive Sleep Apnea

Where it's being run

1 sites across 1 states
Florida1

Study leadership

  • Girardin Jean-Louis, PhD · PRINCIPAL_INVESTIGATOR · University of Miami

Who to contact

Girardin Jean-Louis, PhD
[email protected]
3052430776
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Self-reported race/ethnicity as African American, African, Caribbean or black
Ages 60-85 years
accessible by phone
OSA diagnosis
consent, including permission to release medical data

Exclusion

progressive illnesses in which disability or death is expected within 1 year
impaired cognitive/ functional ability precluding participation
intention to move within the year
and a family member currently enrolled.

What this trial measures

  • Proportion of participants adherence to OSA treatmentUp to 6 months

    The proportion of participants who answer yes (meaning a participant acknowledges an average of more than 4 hours of continuous positive airway pressure use) or no (meaning a participant acknowledges an average of less than 4 hours of continuous positive airway pressure use).