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Clinical Trials/NCT05127330
NCT05127330CompletedNot Applicable

Pilot RCT of a Video-based Intervention for Suicide Prevention

Butler Hospital1 site in 1 country40 target enrollmentStarted: January 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Client Satisfaction Questionnaire (CSQ)

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

LifePlans

Experimental

LifePlans 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.

Intervention: LifePlans (Behavioral)

Treatment as Usual

Active Comparator

Individuals will receive unrestricted routine care only.

Intervention: Treatment as Usual (Behavioral)

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)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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