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Development of a Video-based Intervention for Suicide Prevention

Sponsor
Butler Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04307394
Collaborator
National Institute of Mental Health (NIMH) (NIH)
10
Enrollment
1
Location
1
Arm
9.1
Actual Duration (Months)
1.1
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The investigators will develop a brief video-based intervention for suicide prevention, called LifePlans. LifePlans will be tested in an initial open trial (n = 10) 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: LifePlans
 N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Development of an Adjunctive Video-Based Suicide Prevention Intervention Immediately Following Psychiatric Hospitalization: Open Trial
Actual Study Start Date :
Jul 29, 2021
Actual Primary Completion Date :
May 1, 2022
Actual Study Completion Date :
May 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: LifePlans

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.

Behavioral: LifePlans
LifePlans is a video-based intervention, in which patients watch episodes starting during a psychiatric hospitalization and continuing through 1 month post-discharge.

Outcome Measures

Primary Outcome Measures

  1. 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

  1. 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Butler Hospital Providence Rhode Island United States 02906

Sponsors and Collaborators

  • Butler Hospital
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Brandon Gaudiano, PhD, Butler Hospital
  • Principal Investigator: Lisa Uebelacker, Ph.D., Butler Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Butler Hospital
ClinicalTrials.gov Identifier:
NCT04307394
Other Study ID Numbers:
  • 1910-001
  • R34MH119414
First Posted:
Mar 13, 2020
Last Update Posted:
Jun 10, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Butler Hospital
video intervention
treatment development
open trial
Additional relevant MeSH terms:
Suicide

Study Results

No Results Posted as of Jun 10, 2022