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Clinical Trials/NCT05127330
NCT05127330
Completed
Not Applicable

Pilot RCT of a Video-based Intervention for Suicide Prevention

Butler Hospital1 site in 1 country40 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicidal Ideation
Sponsor
Butler Hospital
Enrollment
40
Locations
1
Primary Endpoint
Client Satisfaction Questionnaire (CSQ)
Status
Completed
Last Updated
11 months ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
November 30, 2023
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Client Satisfaction Questionnaire (CSQ)

Time Frame: 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 Outcomes

  • Columbia Suicide Severity Rating Scale (C-SSRS)(1 Month)

Study Sites (1)

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