Sleep Health Education and Social Support Among Blacks With OSA



Status:Recruiting
Conditions:Insomnia Sleep Studies, Pulmonary
Therapuetic Areas:Psychiatry / Psychology, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - Any
Updated:6/8/2018
Start Date:November 2015
End Date:December 2019
Contact:Azizi Seixas, MD
Email:Azizi.Seixas@nyumc.org

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Tailored Peer-Based Sleep Health Education and Social Support Among Blacks With Obstructive Sleep Apnea

The primary purpose of this study is to ascertain the effectiveness of tailored, peer based
sleep health education and social support in increasing adherence rates to recommended
Obstructive Sleep Apnea (OSA) evaluation and treatment among blacks at risk of Obstructive
Sleep Apnea.

Obstructive sleep apnea (OSA), which disproportionately affects blacks (31% vs. 10%, whites),
is a critical, preventable and/or treatable disease potentially causing increased
cardiovascular disease (CVD) outcomes (e.g., obesity, diabetes, hypertension, stroke,
arrhythmia, and chronic heart failure). Improving sleep may have direct effects in reducing
CVD risk,2 enhancing brain functions, and increasing workplace productivity. Unfortunately,
our focus groups suggest that most at-risk blacks are unaware of OSA symptoms or its related
morbidity. Thus, it is imperative to address poor adherence among blacks with OSA, if we are
to reduce health disparities associated with CVD outcomes between blacks and whites.

This is a randomized study with a total of 6 sites recruiting; 3 will serve as controls and 3
that will be intervention. Group A participants (Intervention group) will receive health
education from a trained Peer Health Educator and Group B participants (Control group) will
meet with a salon worker, barbershop worker, or church Health Ministry group leader.
Participants will be asked to use a sleep diary and wear a home sleep test device to measure
sleep for 7 days. They will be followed for 12 months.

Inclusion Criteria:

- self-reported race/ethnic minority

- ages ≥18 years

- accessible by telephone

- consent to participate, which includes permission to release medical record
information

- A positive screening for OSA is necessary to be enrolled in the intervention protocol.

Exclusion Criteria:

- are involved in another sleep study.

- are unable to understand and sign this informed consent form.

- know someone who is participating in this study.

- had a heart attack or stroke within the past 12 weeks.

- do not identify yourself as a racial/ethnic minority.

- are pregnant.

- Refuse to use the ARESTM home sleep test device.

- Refuse to use the WatchPATTM home sleep test device.

- are not at risk for sleep apnea.
We found this trial at
1
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550 1st Ave
New York, New York 10016
(212) 263-7300
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