RecruitingNot ApplicableNCT06963463

Transdiagnostic Sleep and Circadian Intervention + Bright Light in Adolescents With Elevated Depression (TranS-C+BL)

Transdiagnostic Sleep and Circadian Intervention + Bright Light in Adolescents With Elevated Depression


Sponsor

University of Pittsburgh

Enrollment

90 participants

Start Date

May 6, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to adapt a sleep intervention for individuals representative of all demographic groups, including those who are at the highest risk for suicidal behavior. Sleep difficulties are a promising target for youth with suicidal thoughts and behavior to focus on as a prevention measure. We aim to increase intervention acceptability and impact by adapting it for the adolescent populations at highest risk for suicidal thoughts and behavior. The research project will compare Transdiagnostic Sleep and Circadian Intervention (TranS-C), an evidence based, modularized intervention that targets a range of sleep difficulties to a treatment as usual or control condition including providing weekly sleep feedback reports from data entered into a daily sleep diary and from wearing a sleep sensing, actigraphy watch. Participants in both conditions (TranS-C vs. Sleep Feedback) will wear an actigraphy sleep watch that monitors sleep, and complete daily sleep diaries via smartphone or email. Participants in the TranS-C condition will also wear bright light (BL) and blue blocking glasses each day as well as attend weekly or biweekly sessions with a Sleep Therapist. The sleep therapist will review sleep feedback during sessions.


Eligibility

Min Age: 12 YearsMax Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a sleep-focused therapy combined with bright light treatment to help teenagers with moderate-to-severe depression who also have sleep problems. The goal is to see if improving sleep can ease depression symptoms. **You may be eligible if...** - You are a teenager between 12 and 18 years old - You have moderate to severe depression (based on a standard questionnaire score of 11 or higher) - You have significant sleep disturbances - You speak and read English well enough to follow the program **You may NOT be eligible if...** - You have obstructive sleep apnea - You have restless legs syndrome - You have symptoms of psychosis - You have bipolar disorder Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALTranS-C

This intervention includes participants attending 6-8 sessions with a Sleep Therapist.

BEHAVIORALSleep Feedback

Participants are provided with an actigraphy watch that is used to monitor their sleep and activity throughout the day and complete a sleep diary daily. Along with wearing the watch they also will be provided access to their actigraphy and sleep diary graphs that document their data.


Locations(2)

Childrens Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

University of Pittsburgh

Pittsburgh, Pennsylvania, United States

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NCT06963463


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