NCT06139861NARecruiting
Better Sleep Study
Children's Hospital Los Angeles
Start Date
3/15/2024
Completion Date
8/1/2028
Summary
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.
Eligibility Criteria
Age Range: 12 years to 18 years
Inclusion Criteria:
Exclusion Criteria:
* 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
Interventions
BEHAVIORAL
TranS-C
BEHAVIORAL
Psychoeducation
Conditions
Depression in AdolescenceDelayed Sleep Phase
Locations
Children's Hospital Los Angeles
Los Angeles, California 90027
United States