- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05102175
Addressing Health Disparities in African Americans - Exploring Sleep and Developing Interventions (HD-SLEEP1)
Study Overview
Detailed Description
African Americans (AAs) sleep worse than whites on average, thus contributing to race disparities in major health outcomes. However, contributors to poorer sleep and effective interventions to improve sleep among AAs is lacking due to under-representation of AAs in sleep research. The investigators propose to address this knowledge gap through engagement with the Baton Rouge African American community. The investigators will use focus groups to determine sleep-related perceptions as well as barriers to sleep research recruitment and retention.
In this study, up to 60 African Americans who self-report poor sleep will be invited to participate in focus group discussions to understand 1) sleep related perceptions; 2) factors influencing participation; and 3) willingness to undertake study procedures typical of sleep research studies such as increasing sleep duration, diagnosing and treating OSA; along with other routine research procedures including blood draws, caloric restriction, and body composition exams.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Louisiana
-
Baton Rouge, Louisiana, United States, 70808
- Recruiting core Pennington
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Self-identified African American
- Age range: >18 years (inclusive)
- Sex: Both males and females will be allowed to participate in the study
- Self-perceived poor sleep
- Willing to be audio and video recorded
Exclusion Criteria:
- Unable to provide written informed consent
- Unable to understand English
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
African American adults with poor sleep
Individuals with self-identified poor sleep quality and/or quantity
|
Eligible participants will be invited to a semi-structured focus group discussion.
Each group will include 8 -12 participants.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Importance of Sleep
Time Frame: 1 day
|
Identify if sleep is considered important for health
|
1 day
|
|
Knowledge related to components of good sleep
Time Frame: 1 day
|
Identify adequate sleep duration, good sleep quality, and absence of sleep disorders as important.
|
1 day
|
|
Perceived advantages related to participating in sleep-related
Time Frame: 1 day
|
May improve health and quality of life
|
1 day
|
|
Identify what challenges prevents participation in sleep-related research
Time Frame: 1 day
|
Willingness to undertake sleep related study procedures and time commitment
|
1 day
|
|
Identify facilitators to participation in sleep research
Time Frame: 1 day
|
At-home assessments, study location, number of study visits
|
1 day
|
Collaborators and Investigators
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PBRC 2020-020-1
- U54GM104940 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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