Sleep and Circadian Interventions for College Students at High Risk of Suicide
Recruiting now · Not applicable
Conditions studied: Sleep Disturbance, Sleep, Depression, Suicide
In brief
The purpose of this study is to examine the extent to which delivering sleep and circadian focused interventions in addition to evidenced based psychiatric care for depression and suicide risk may contribute to decreasing suicide risk among high risk young adults. Investigators will evaluate three interventions targeting sleep in acutely suicidal college students enrolled in intensive outpatient treatment. Participants will be randomly assigned to one of three intervention groups: 1. Triple Chronotherapy (TCT)+ Transdiagnostic Sleep and Circadian Intervention (TSC) 2. Transdiagnostic Sleep and Circadian Intervention (TSC) 3. Sleep Feedback (SF) Participants will be followed for 6 months with primary outcome domains of suicidal thoughts and behaviors and depression evaluated by blinded clinicians at short (Days 1-4 of intervention), medium (2 months) and long (6 month) term intervals.
Key facts
- Study ID
- NCT07346014
- Run by
- University of Pittsburgh
- People needed
- 90
- Starts
- 2026-06-18
- Expected to finish
- 2029-03-01
- Last updated by the study team
- 2026-07-07
Who can join
Age: 18 and older, up to 25. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Enrolled or planning to enroll in treatment at COSTAR Intensive Outpatient Program
- English language fluency and literacy sufficient to engage in study protocol
- Suicidal ideation or suicide attempt in past month
- Clinically significant sleep disturbance, operationalized as Pittsburgh Sleep Quality Index global PSQI score >= 7, and/or delayed bedtimes (>midnight), and/or >2 hours in sleep timing variability
You may not qualify if…
- Non-affective psychosis per electronic health record (EHR) review and/or baseline clinical assessment, or symptom severity or psychosocial functioning impairments that preclude participation
- Contraindications for either sleep deprivation or bright light therapy (e.g., bipolar disorder; seizure disorder; photosensitizing medication)
- Intellectual disability precluding comprehension of study procedures
- Evidence of untreated obstructive sleep apnea and/or restless legs syndrome
- Life-threatening medical condition requiring immediate treatment (such as cancer; end stage disease)
- Pregnancy
Where it is running
- Western Psychiatric Hospital/University of Pittsburgh — Pittsburgh, Pennsylvania, United States (enrolling)
Full record on ClinicalTrials.gov
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