Study Summary
This trial is looking at how well sleep and circadian health affects obese adolescents who are undergoing bariatric surgery. They will be evaluated at 1 year to see how well they sleep and how it affects their weight loss and insulin sensitivity.
Eligible Conditions
- Sleep
Treatment Effectiveness
Study Objectives
1 Primary · 0 Secondary · Reporting Duration: 1 week
1 week
Sleep duration
Trial Safety
Trial Design
1 Treatment Group
Sleep Extension
1 of 1
Experimental Treatment
26 Total Participants · 1 Treatment Group
Primary Treatment: PBS Study · No Placebo Group · N/A
Sleep Extension
Behavioral
Experimental Group · 1 Intervention: PBS Study · Intervention Types: BehavioralTrial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: 1 week
Who is running the clinical trial?
University of Colorado, DenverLead Sponsor
1,608 Previous Clinical Trials
1,932,653 Total Patients Enrolled
5 Trials studying Sleep
220 Patients Enrolled for Sleep
Jill L Kaar, PhDPrincipal InvestigatorUniversity of Colorado Denver | Anschutz
1 Previous Clinical Trials
867 Total Patients Enrolled
Eligibility Criteria
Age 14 - 19 · All Participants · 4 Total Inclusion Criteria
Mark “Yes” if the following statements are true for you:You are currently in high school and may not be getting enough sleep.
You must have completed puberty and have physical characteristics consistent with Tanner Stage 5.
Who else is applying?
What state do they live in?
| Colorado | 100.0% |
How old are they?
| 18 - 65 | 100.0% |
What site did they apply to?
| Children's Hospital Colorado | 100.0% |
What portion of applicants met pre-screening criteria?
| Met criteria | 100.0% |