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Clinical Trials/NCT04903431
NCT04903431
Completed
Not Applicable

Assessing the Effectiveness of Self- and Clinician-administered Crisis Response Planning for Suicide Risk

Ohio State University1 site in 1 country75 target enrollmentDecember 15, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicide, Attempted
Sponsor
Ohio State University
Enrollment
75
Locations
1
Primary Endpoint
Change in Suicide Visual Analog Scale scores from the previous daily assessment
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of the current project is to compare the use and preliminary effectiveness of a self-administered version of the Crisis Response Plan (CRP) in decreasing suicidal/death ideation and distress and increasing positive affect when compared to a clinician-administered version of the protocol in a sample of 150 military Veterans experiencing current death or suicidal ideation.

Registry
clinicaltrials.gov
Start Date
December 15, 2021
End Date
February 21, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lauren Khazem

Principal Investigator

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • US military veteran
  • death or suicidal ideation/suicide attempt within the past month

Exclusion Criteria

  • non-Veteran status
  • acute intoxication or active psychosis precluding provision of informed consent
  • inability to communicate and comprehend English
  • residence outside the United States
  • lack of past-month death/suicide ideation or attempt
  • lack of device connected to webcam or internet

Outcomes

Primary Outcomes

Change in Suicide Visual Analog Scale scores from the previous daily assessment

Time Frame: Administered daily for eight consecutive days

The Suicide Visual Analog Scale The S-VAS assesses "urge to kill myself" using a horizontal line with anchors on the left reflecting "none" (score: 0) and on the right reflecting "extreme" (score: 100). The S-VAS is initially presented with the indicator on the "none" position, and non-movement of the indicator is followed by a prompt to remind the participant to move the indicator, if relevant, to ensure response accuracy. Higher scores are indicative of greater severity

Secondary Outcomes

  • Change in Patient Health Questionnaire - 2 scores from the previous daily assessment(Administered daily for eight consecutive days)
  • Change in Positive and Negative Affect Schedule - Short Form scores from the previous daily assessment(Administered daily for eight consecutive days)
  • Change in Crisis Response Plan Use from the previous daily assessment(Administered daily for eight consecutive days)

Study Sites (1)

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