No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
12 – 18
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
90 (estimated)
Sponsor
University of Pittsburgh · Other
Who this trial is looking for
This trial is looking for teenagers who are dealing with depression and sleep issues. Participants will take part in a program that helps improve sleep and includes wearing a special light and completing daily sleep diaries.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 12 and 18 years old.
I have moderate to severe depression.
I have significant sleep problems.
I can read and understand English well.
You may not be able to join if
I have obstructive sleep apnea.
I have restless legs syndrome.
I have psychosis.
I have bipolar disorder.
I have a developmental disability that affects understanding.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 adole…
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adolescents (12-18)
* Current moderate to severe depression as measured by the PHQ-9M with a total score of greater than or equal to 11
* Current clinically significant sleep disturbance measured by the PHQ-9-M sleep item greater than or equal to 2.
* English language fluency …
Inclusion Criteria:
* Adolescents (12-18)
* Current moderate to severe depression as measured by the PHQ-9M with a total score of greater than or equal to 11
* Current clinically significant sleep disturbance measured by the PHQ-9-M sleep item greater than or equal to 2.
* English language fluency and literacy sufficient to engage in study protocol.
Exclusion Criteria:
* Evidence of obstructive sleep apnea,
* Evidence of restless legs syndrome
* Evidence of psychosis
* Evidence of bipolar disorder
* Evidence of a developmental disability precluding comprehension of study procedures per electronic health record and eligibility screening.
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