RecruitingDepression in AdolescenceDelayed Sleep Phase
Better Sleep Study
Eligible age
12–18 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
See if you qualify for this study
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About this study
The overall aim of this proposal is a confirmatory efficacy trial sufficiently powered and designed to test the hypothesis that improving the relationship between biological circadian timing and waketime, a novel modifiable target, improves depression outcomes in a subgroup of adolescents with depression and a misaligned relationship between biological circadian timing and waketime utilizing a cognitive-behavioral sleep intervention.
Sponsor: Children's Hospital Los Angeles
You may not qualify if…
- ✕ mental health/behavioral symptoms that would preclude productive engagement in study assessments or intervention (e.g., active psychosis; Bipolar Disorder; drug dependence
- ✕ severe or unstable medical or psychiatric condition such that treatment has changed within the last month or is expected to change during the course of the study or that would preclude ability to adhere to study procedures (e.g. terminal end-stage cancer)
- ✕ current use of medications or herbs with known effects on sleep
- ✕ plan to undergo or have had medication change in the last 8 weeks
Where it's recruiting
California
Los Angeles
Source: ClinicalTrials.gov · NCT06139861 · last updated 2026-05-11