Addressing Health Disparities in African Americans - Exploring Sleep and Developing Interventions - 2

NCT ID: NCT05102188

Last Updated: 2023-02-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

80 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-11

Study Completion Date

2022-12-31

Brief Summary

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The purpose of the HD-SLEEP2 study is to help researchers understand sleep in African Americans. The investigators also want to know what factors may affect sleep.

Detailed Description

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African Americans who self-report poor sleep (n=80) will be invited to complete questionnaire based self-assessment of known factors and comorbidities contributing to alterations in sleep such as demographic characteristics, anthropometrics, depression, insomnia, and food habits in conjunction with objective and subjective measures of sleep via 7-day accelerometry (sleep duration), overnight oximetry (sleep apnea), and sleep questionnaires.

Conditions

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Sleep

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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African American adults with poor sleep

Individuals with self-identified poor sleep quality and/or quantity

Assessment of sleep and related factors

Intervention Type COMBINATION_PRODUCT

Eligible participants will be invited to fill out several forms and wear a watch-like device on their wrist (an accelerometer) for 7 days to assess their sleep habits. They will also be asked to sleep at home with a watch-like device attached to a sleeve which covers their index finger (an oximeter) for one night to assess whether they may have a sleep problem like sleep apnea.

Interventions

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Assessment of sleep and related factors

Eligible participants will be invited to fill out several forms and wear a watch-like device on their wrist (an accelerometer) for 7 days to assess their sleep habits. They will also be asked to sleep at home with a watch-like device attached to a sleeve which covers their index finger (an oximeter) for one night to assess whether they may have a sleep problem like sleep apnea.

Intervention Type COMBINATION_PRODUCT

Eligibility Criteria

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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

Exclusion Criteria

* Unable to provide written informed consent
* Unable to understand English
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of General Medical Sciences (NIGMS)

NIH

Sponsor Role collaborator

Pennington Biomedical Research Center

OTHER

Sponsor Role lead

Responsible Party

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Prachi Singh

Associate Professor, Sleep and Cardiometabolic Health

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Prachi Singh, PhD

Role: PRINCIPAL_INVESTIGATOR

Pennington Biomedical Research Center

Locations

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Recruiting core Pennington

Baton Rouge, Louisiana, United States

Site Status

Countries

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United States

Other Identifiers

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U54GM104940

Identifier Type: NIH

Identifier Source: secondary_id

View Link

PBRC 2020-020-2

Identifier Type: -

Identifier Source: org_study_id

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