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OpenTrials
Completed

NCT Number: NCT02507089

Tailored Approach to Sleep Health Education: A Community Engaged Approach

This study aims to develop educational tools and platforms to promote the transfer of sleep health information to blacks to foster adoption of healthful sleep practices.

Completed

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Key information

Conditions

Healthcare Disparities Mental Disorders Minority Health Nervous System Diseases Neurologic Manifestations Pathological Conditions, Signs and Symptoms Signs and Symptoms Sleep Sleep Disorders Sleep Wake Disorders

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

NYU Langone Medical Center

New York, 10016, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • self-reported race/ethnicity as African American, African, Caribbean American or black men and women; ages ≥18 years;
  • accessible by telephone; no plans to move away from the region within the year following enrollment;
  • consent to participate, which includes permission to release medical record information;
  • documented OSA risk based on scores received from the Apnea Risk Evaluation System questionnaire

Exclusion criteria

  • progressive medical illness in which disability or death is expected within one year;
  • impaired cognitive or functional ability which would preclude meaningful participation in the study;
  • sleep apnea diagnosis;
  • stated intention to move within the same year of enrollment.

Treatment and study plan

Tailored sleep health education materials.

Behavioral

Tailored sleep health materials.

Generic sleep health education materials.

Behavioral

Primary outcomes

  1. Sleep Hygiene Index

    Time frame: 6 months

  2. Apnea Knowledge/Apnea Belief Scale

    Time frame: 6 months

  3. Self-Efficacy Scale

    Time frame: 6 months

  4. Change Assessment Scale

    Time frame: 6 months

Secondary outcomes

  1. 7-Day Physical Activity Recall

    Time frame: 6 months

  2. By-Meal Fruit/Vegetable Intake Screener

    Time frame: 6 months

  3. Rapid Estimate of Adult Literacy in Medicine

    Time frame: 6 months

  4. Medical Outcomes Study Short Form 36

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

NYU Langone Health

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

Registry information

Acronym: TASHE

Important dates

Study start
2014
Primary completion
2017
Study completion
2018
First posted
Jul 23, 2015
Registry last updated
Jun 27, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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