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

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The Ohio State University

Status

Completed

Conditions

Suicide, Attempted
Suicidal Ideation

Treatments

Behavioral: Crisis Response Planning for Suicide Risk

Study type

Interventional

Funder types

Other

Identifiers

NCT04903431
2020B0414-B

Details and patient eligibility

About

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.

Enrollment

75 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

75 participants in 2 patient groups

Clinician-administered Crisis Response Plan
Active Comparator group
Description:
Clinicians will administer the Crisis Response Plan to 75 military veterans.
Treatment:
Behavioral: Crisis Response Planning for Suicide Risk
Self-administered Crisis Response Plan
Experimental group
Description:
Participants will complete a self-guided version of the Crisis Response plan online.
Treatment:
Behavioral: Crisis Response Planning for Suicide Risk

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Lauren Khazem, PhD

Data sourced from clinicaltrials.gov

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