The Reducing Risk Study

University of California San Francisco (UCSF)

Status: Enrolling

Conditions: Delayed Sleep Phase; Insomnia

Treatments: Behavioral: Control; Behavioral: mTranS-C

Study type: Interventional

Funder types: Other

Identifiers

NCT03665337

IRB-47676

Details and patient eligibility

About

The present study will test an innovative mobile health adaptation of a behavioral intervention that improves sleep and mental health concerns among adolescents.

Enrollment: 60 estimated patients

Sex: All

Ages: 12 to 18 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Exclusion Criteria:

• any current psychiatric illness
• currently use of medications or herbs with known effects on sleep
• hospitalization for substance use or suicide within the past 12 months
• known sleep apnea
• unstable major medical conditions
• current psychotherapy for depression, anxiety or sleep health deficits

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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60 participants in 2 patient groups

mTranS-C

Experimental group

Description:

Access to a mobile and computer accessible adaptation of Transdiagnostic Sleep and Circadian Intervention

Treatment:

Behavioral: mTranS-C

Control

Active Comparator group

Description:

Access to a mobile and computer accessible control intervention that targets coping skills and sleep education.

Treatment:

Behavioral: Control