The primary objective of this study is to assess the effectiveness of a digital intervention in reducing suicide attempts.
This double blind, randomized controlled trial will evaluate effectiveness of two digital interventions among 391 participants. Study participation will start when participants sign consent. Participants and research assessors will be blinded to treatment assignment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
356
Experimental Pscyhoeducation and Intervention App
Other Pscyhoeducation App
Treatment as usual may include appointments with psychiatrists and other mental health clinicians, suicide risk assessment, supportive listening, crisis resources, clinician assessment, and referral to outpatient treatment.
UCDDenver / Denver Health
Denver, Colorado, United States
Yale
New Haven, Connecticut, United States
Common Spirit
Omaha, Nebraska, United States
Northwell Health
Glen Oaks, New York, United States
Columbia-Suicide Severity Rating Scale(C-SSRS)
The C-SSRS will be used to assess change in suicide behaviors at 8 separate time points from screening period to Week 104.
Time frame: Screening, Week 4, Week 8, Week 12, Week 24, Week 52, Week 78, Week 104
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
University of Cincinnati
Cincinnati, Ohio, United States
Harding Hospital
Columbus, Ohio, United States