Improving Sleep Health for Asian Americans
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-70
SponsorNew York University
About this trial
Filipino Americans are at high risk of poor sleep and its adverse health consequences. The goal of this study is to test a generative AI-powered chatbot that delivers personalized, evidence-based sleep education and guidance to Filipino Americans who experience poor sleep.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 30 to 70 years
Self-identify as having a Filipino background and reside in the United States
Poor sleep quality, defined as a Pittsburgh Sleep Quality Index (PSQI) score ≥ 5
Short sleep duration, defined as an average Fitbit-measured total sleep time < 7 hours/night over 7 days
Disqualifiers
Severe mental disorders, including major depressive symptoms
Medical conditions, including cognitive impairment, that may interfere with the ability to follow study procedures
Current participation in another lifestyle intervention
Night-shift or rotating-shift worker
Trial design
Design model
Single group
Treatments tested in this trial
Intervention Group
BehavioralParticipants engage with an AI chatbot for two weeks to learn personalized education and skills regarding sleep promotion
Treatment groups
40 Participants
are divided into 1 treatment groupGroup A: InterventionExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Intervention retention
Percentage of participants who complete the 2-week sleep intervention
Time frame
From enrollment to 2-week post-interventionSecondary outcomes
1
Feasibility of recruitment
Percentage of adults who meet the study criteria
Time frame
From screening to baseline2
Feasibility of study enrollment
Percentage of eligible participants who provide consent
Time frame
From screening to enrollment3
Feasibility of completing the study assessment
Percentage of enrolled participants who complete the baseline assessment
Time frame
From enrollment to baseline4
Feasibility of completing the study assessment
Percentage of enrolled participants who complete the post-intervention assessment
Time frame
From enrollment to 2-week post-interventionSponsors and contacts
Click on the lead sponsor to view all of their trials.
New York University
Lead sponsor
National Institute on Minority Health and Health Disparities (NIMHD)
Collaborator
Source ClinicalTrials.gov
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