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personalized behavioral recommendations for Insomnia
N/A
Waitlist Available
Research Sponsored by Howard University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Inclusion Criteria:1. Healthy adults age 18 - 35, self-identified as Black or African American, born in the United States.
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
This trial is testing whether providing feedback and recommendations on how to cope with potentially sleep-disruptive cognitions can help improve sleep efficiency.
Eligible Conditions
- Insomnia
- Post-Traumatic Stress Disorder
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
sleep efficiency
Secondary outcome measures
normalized high frequency ratio of heart rate variability while in bed
pulse wave velocity
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: personalized behavioral recommendationsExperimental Treatment1 Intervention
Will receive recommendations for altering sleep related behavior based on data from in-home monitoring.
Group II: educational controlActive Control1 Intervention
Will receive the data without recommendations. Will receive personalized recommendations after the follow up assessment.
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Who is running the clinical trial?
Howard UniversityLead Sponsor
39 Previous Clinical Trials
13,079 Total Patients Enrolled
1 Trials studying Insomnia
41 Patients Enrolled for Insomnia
Frequently Asked Questions
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