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Evaluation of the Coping Long Term With Active Suicide Program

Not Applicable
Completed
Conditions
Suicide
Interventions
Behavioral: SAFE
Behavioral: CLASP
Registration Number
NCT02313753
Lead Sponsor
Butler Hospital
Brief Summary

The purpose of this study is to evaluate the utility of the Coping Long Term with Active Suicide Program (CLASP) for reducing suicidal behavior.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
224
Inclusion Criteria
  1. Current patient at Butler Hospital
  2. Suicide attempt or suicidal ideation with intent to make a suicide attempt within 48 hours of hospitalization as indicated on the hospital chart and confirmed by administration of the C-SSRS
  3. Age > 18 years
  4. Have a reliable telephone
  5. Ability to speak, read, and understand English well to complete the procedures of the study
Exclusion Criteria
  1. Current psychotic symptoms severe enough to impair study participation

  2. Participation in a treatment program with established efficacy in preventing suicidal behavior

  3. Cognitive impairment which would interfere with adequate participation in the project (MMSE< 20).

  4. Currently in state custody or pending legal action 5. Already enrolled current or previous CLASP trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SAFESAFESafety Assessment and Follow-up Evaluation Protocol
CLASPCLASPCoping Long Term with Active Suicide Program Protocol
Primary Outcome Measures
NameTimeMethod
A composite composed of the number of participants with either a suicide attempt or death by suicide52 weeks following discharge from hospital

As assessed by both the Columbia Suicide Severity Rating Scale and record review

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Butler Hospital

🇺🇸

Providence, Rhode Island, United States

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