- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03389828
Qualitative Study of Black-White Sleep Disparities
Background:
Sleep that does not last long and is low-quality is tied to a range of serious health issues. These range from obesity to early death. Research has shown that black people who are professionals or managers are more likely to have this kind of sleep than their white counterparts. Black people are also at higher risk than whites for health problems caused by insufficient sleep. Researchers want to learn more about why these differences exist.
Objective:
To study reasons for racial differences in the work-sleep relationship.
Eligibility:
Adults at least 25 years old who:
- Are non-Hispanic black or non-Hispanic white
- Are employed and work 38 or more hours a week
- Live around Raleigh-Durham-Chapel Hill, NC, or Washington, DC
Design:
Participants will be screened with questions. They will give sociodemographic data like job title, annual income level, and gender. They will give their contact information.
Participants will have 1 study visit. They will be in a closed, private conference room. They will join a focus group. The focus groups will be organized by to race, gender, and occupational class.
Participants will give informed consent before the focus group begins.
During the focus group, participants will be asked about their perceptions of health in general, and their typical work day. They will be asked about sleep.
Participants will also fill out a short questionnaire about their job and sleep habits.
Focus groups will be audio recorded. The entire session will last 90 to 120 minutes.
Study Overview
Status
Conditions
Detailed Description
OBJECTIVE:
Prior research has documented racial differences in sleep health by occupational class. While increasing professional responsibility has been associated with shorter sleep duration among non-Hispanic Blacks, increasing professional responsibility appears to be associated with a lower prevalence of short sleep duration among non-Hispanic Whites. The objective of the present study is to investigate reasons for these racial differences in the work-sleep relationship.
STUDY POPULATION:
The study population will consist of approximately 340 focus groups participants. All non-Hispanic black and white adults 25 years of age or older who are currently working at least 38 hours a week will be eligible for inclusion in the study. To mitigate the influence of known cultural differences in sleep behaviors, participation will be limited to English speakers born in the continental United Sates.
DESIGN:
We will conduct 34 demographically homogenous focus groups consisting of 7-12 participants each. Focus groups will be stratified based race, gender, and occupational class, and will be conducted in both North Carolina and the metropolitan DC area. Focus groups will take place in-person and be conducted by a trained facilitator according to a scripted, semi-structured focus group guide. Audio recordings of the focus groups will be transcribed verbatim by a professional transcription service. De-identified transcripts will be reviewed by the study team to identify qualitative themes in the data, which will be coded in an appropriate software program using a double-coding process. Qualitative data analysis will be conducted to identify potential reasons for racial differences in sleep health by occupational class. We will additionally assess variation by other sociodemographic determinants, including gender, education, income, and geographic region.
OUTCOMES MEASURES:
Outcome measures include the themes/patterns regarding potential system-level influences, beliefs, and behaviors that may explain racial differences in the association between occupational class and sleep health.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Maryland
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Silver Spring, Maryland, United States, 20910
- Social and Scientific Systems, Inc.
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North Carolina
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Durham, North Carolina, United States, 27703
- Social and Scientific Systems, Inc.
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
- INCLUSION CRITERIA:
- Non-Hispanic Black or non-Hispanic White
- Female or Male
- 25 years of age or older
- Employed (38 plus hours/week)
- Residing in the area around of Raleigh-Durham-Chapel Hill, NC or Silver Spring, MD
EXCLUSION CRITERIA:
- Born outside the continental United States
- Not fluent in English
- Unwilling to provide answers to all screening questions
- Unwilling to provide informed consent
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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1
The study population will consist of approximately 340 focus groups participants.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Outcome measures include the themes/patterns regarding potential system-level influences, beliefs, and behaviors that may explain racial differences in the association between occupational class and sleep health.
Time Frame: At the time of the focus group and in more detail during data analysis (coding)
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Data will be analyzed via qualitative coding software to identify themes/patterns in the narratives of participants in focus groups and interviews.
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At the time of the focus group and in more detail during data analysis (coding)
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Collaborators and Investigators
Investigators
- Principal Investigator: Chandra L Jackson, Ph.D., National Institute of Environmental Health Sciences (NIEHS)
Publications and helpful links
General Publications
- Luckhaupt SE, Tak S, Calvert GM. The prevalence of short sleep duration by industry and occupation in the National Health Interview Survey. Sleep. 2010 Feb;33(2):149-59. doi: 10.1093/sleep/33.2.149.
- Jackson CL, Redline S, Kawachi I, Williams MA, Hu FB. Racial disparities in short sleep duration by occupation and industry. Am J Epidemiol. 2013 Nov 1;178(9):1442-51. doi: 10.1093/aje/kwt159. Epub 2013 Sep 9.
- Krueger PM, Friedman EM. Sleep duration in the United States: a cross-sectional population-based study. Am J Epidemiol. 2009 May 1;169(9):1052-63. doi: 10.1093/aje/kwp023. Epub 2009 Mar 18.
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
Other Study ID Numbers
- 999918021
- 18-E-N021
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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