Addressing Health Disparities in African Americans - Exploring Sleep and Developing Interventions (HD-SLEEP1)

August 24, 2022 updated by: Prachi Singh, Pennington Biomedical Research Center
The purpose of the HD-SLEEP1 study is to help researchers understand what African Americans know and think about sleep. The investigators also want to know how to encourage people to participate in research studies designed to improve sleep.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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

Observational

Enrollment (Actual)

36

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Louisiana
      • Baton Rouge, Louisiana, United States, 70808
        • Recruiting core Pennington

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

African Americans residing in Greater Baton Rouge area will be invited to participate in the study.

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

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 Major Dates

Study Start (Actual)

November 1, 2021

Primary Completion (Actual)

August 24, 2022

Study Completion (Actual)

August 24, 2022

Study Registration Dates

First Submitted

October 20, 2021

First Submitted That Met QC Criteria

October 20, 2021

First Posted (Actual)

November 1, 2021

Study Record Updates

Last Update Posted (Actual)

August 29, 2022

Last Update Submitted That Met QC Criteria

August 24, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

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)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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