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Pilot RCT of a Video-based Intervention for Suicide Prevention

Not Applicable
Completed
Conditions
Suicidal Ideation
Suicide
Suicidal Behaviors
Interventions
Behavioral: Treatment as Usual
Behavioral: LifePlans
Registration Number
NCT05127330
Lead Sponsor
Butler Hospital
Brief Summary

The investigators will develop a brief video-based intervention for suicide prevention, called LifePlans. LifePlans will be tested in a pilot randomized controlled trial (n = 40) to examine its feasibility and acceptability. Investigators will recruit patients admitted to a psychiatric hospital for suicidal thoughts and behaviors who will receive the intervention for 4 weeks post-discharge. Patients will be assessed at hospital baseline, 1 month post-discharge, and 6 months post-discharge.

Detailed Description

In this project, we propose to develop a new intervention, called LifePlans. LifePlans will consist of brief videos that highlight patients' experiences. Episodes will cover these topics: 1) developing a personalized "Life Plan" to stay safe and restrict means, 2) clarifying valued life domains and related goals to improve hopefulness, 3) using informal problem solving to cope better with illness, 4) improving communication with family/friends to increase social support, and 5) adhering to primary treatments including pharmacotherapy and psychotherapy to promote illness management. LifePlans will be tested in a pilot randomized controlled trial (n = 40) to examine its feasibility and acceptability. Investigators will recruit patients admitted to a psychiatric hospital for suicidal thoughts and behaviors who will receive the intervention for 4 weeks post-discharge. Patients will be assessed at hospital baseline, 1 month post-discharge, and 6 months post-discharge.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • current psychiatric hospitalization for suicidal thoughts and behaviors
  • 18 years or older
  • ability to speak and read English
  • access to means for viewing videos (computer, tablet, smartphone)
Exclusion Criteria
  • current psychotic symptoms
  • current cognitive impairment

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Treatment as UsualTreatment as UsualIndividuals will receive unrestricted routine care only.
LifePlansLifePlansLifePlans is a video series using real patients telling their stories of overcoming suicidal thoughts and behaviors to help others who are struggling with these issues.
Primary Outcome Measures
NameTimeMethod
Client Satisfaction Questionnaire (CSQ)1 Month

The Client Satisfaction Questionnaire is a self-report measure of patient satisfaction with treatment. The total score will be used and ranges from 8 to 32 with increased scores indicating greater satisfaction with treatment.

Secondary Outcome Measures
NameTimeMethod
Columbia Suicide Severity Rating Scale (C-SSRS)1 Month

The Columbia Suicide Severity Rating Scale is an interviewer-rated measure of suicidal thoughts and behaviors. The total score (sum of items) will be used and ranges from 2 to 25 with higher scores indicating higher suicidal thoughts and behaviors.

Trial Locations

Locations (1)

Butler Hospital

🇺🇸

Providence, Rhode Island, United States

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