Establishing Efficacy of an Inpatient Intervention and Phone App to Reduce Suicidal Risk
Status: | Not yet recruiting |
---|---|
Conditions: | Psychiatric |
Therapuetic Areas: | Psychiatry / Psychology |
Healthy: | No |
Age Range: | 12 - 17 |
Updated: | 3/23/2019 |
Start Date: | April 1, 2019 |
End Date: | September 2020 |
Contact: | Jessica M. Jones, MA |
Email: | jessica.jones@utsouthwestern.edu |
Phone: | 214-456-3691 |
As Safe As Possible (ASAP): A Balanced, Two-by-Two Design To Test Conjoint and Unique Efficacy of an Inpatient Intervention and an Emotion Regulation/Safety Planning App in Preventing Suicide Attempts Post-Discharge
In this 2-site study, University of Texas Southwestern Medical Center (UTSW) and Western
Psychiatric Institute and Clinic (WPIC), the investigators will conduct a randomized clinical
trial (RCT) in 240 psychiatrically hospitalized suicidal adolescents, examining the single
and additive effects of two components of an inpatient unit intervention for suicidal
adolescents, As Safe As Possible (ASAP), which focuses on emotion regulation and safety
planning, and an emotion regulation/safety plan phone app (BRITE).
Psychiatric Institute and Clinic (WPIC), the investigators will conduct a randomized clinical
trial (RCT) in 240 psychiatrically hospitalized suicidal adolescents, examining the single
and additive effects of two components of an inpatient unit intervention for suicidal
adolescents, As Safe As Possible (ASAP), which focuses on emotion regulation and safety
planning, and an emotion regulation/safety plan phone app (BRITE).
The investigators aim to randomize 240 adolescents psychiatrically hospitalized for suicidal
ideation with a plan or a suicide attempt to one of four treatment arms: (1) ASAP + BRITE +
TAU (treatment as usual); (2) BRITE + TAU (treatment as usual); (3) ASAP + TAU (treatment as
usual); and (4) TAU (treatment as usual) alone. The investigators will assess suicidal
ideation and behavior at 4, 12, and 24 weeks post-intake, in order to:
1. Assess the relative efficacy of ASAP, BRITE and the combination on suicidal ideation,
non-suicidal self-injury (NSSI), and suicide attempts, and re-hospitalizations.
2. Examine mediators and moderators of treatment outcome.
3. Examine the costs and cost efficacy of ASAP and BRITE and the combination.
ideation with a plan or a suicide attempt to one of four treatment arms: (1) ASAP + BRITE +
TAU (treatment as usual); (2) BRITE + TAU (treatment as usual); (3) ASAP + TAU (treatment as
usual); and (4) TAU (treatment as usual) alone. The investigators will assess suicidal
ideation and behavior at 4, 12, and 24 weeks post-intake, in order to:
1. Assess the relative efficacy of ASAP, BRITE and the combination on suicidal ideation,
non-suicidal self-injury (NSSI), and suicide attempts, and re-hospitalizations.
2. Examine mediators and moderators of treatment outcome.
3. Examine the costs and cost efficacy of ASAP and BRITE and the combination.
Inclusion Criteria:
- Youth admitted to the inpatient unit at either site for a recent suicide attempt or
significant suicidal ideation with a plan or intent.
- The youth and parent are able to complete assessments in English, and the youth is
able to complete therapy.
Exclusion Criteria:
- The youth currently exhibits psychosis.
- The youth currently exhibits mania.
- The youth is currently <85% of their ideal body weight.
- The youth is intellectually incapable of completing the study, e.g. has an
intelligence quotient (IQ) < 70.
We found this trial at
2
sites
1801 Inwood Rd
Dallas, Texas 75390
Dallas, Texas 75390
(214) 645-3300
Principal Investigator: Beth D. Kennard, PsyD
Phone: 214-456-3691
University of Texas Southwestern Medical Center UT Southwestern is an academic medical center, world-renowned for...
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4200 Fifth Ave
Pittsburgh, Pennsylvania 15260
Pittsburgh, Pennsylvania 15260
(412) 624-4141
Principal Investigator: David A Brent, MD
Phone: 412-586-9064
University of Pittsburgh The University of Pittsburgh is a state-related research university, founded as the...
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