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Clinical Trials/NCT01355848
NCT01355848
Completed
Phase 1

Improving Care Provided to Patients Treated in a Level 1 Trauma Center Post-suicide Attempt

University of Washington1 site in 1 country40 target enrollmentMay 2011
ConditionsSuicidal Ideas

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Suicidal Ideas
Sponsor
University of Washington
Enrollment
40
Locations
1
Primary Endpoint
Patient Satisfaction Questionnaire
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The aim of the study is to refine, elaborate, and pilot a brief intervention for adult patients following a suicide attempt provided during hospitalization in an acute medical setting. 40 participants will be randomized to receive the brief intervention + care as usual or only care as usual. It is hypothesized that the intervention will be acceptable and feasible to both patients and intervention clinicians.

Detailed Description

The aim of the study is to refine, elaborate, and pilot a brief intervention for adult patients following a suicide attempt provided during hospitalization in an acute medical setting, and will be addressed with a sample of cases (N = 40) from Harborview. The participants will be randomized into one of two groups: those that receive the intervention and those that do not. All participants will complete a battery of assessments The intervention is based on the theory of teachable moments, wherein timing in proximity to injury and appropriate treatment setting provide a unique opportunity to create patient behavioral change. The brief intervention consists of engaging the patient in conversation regarding suicidal ambivalence (desire to live vs. desire to die), collaborative discovery of primary and secondary drivers of suicidality, and safety planning. A guide to delivering the intervention has been completed and may undergo changes throughout the study. Adherence measures will be developed in order to assess the degree to which the clinician accurately provided the brief intervention without including additional therapeutic elements or leaving out elements required in the intervention guide. Best methods for integrating the brief intervention into services provided on medical and surgical units will be determined, as well.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
April 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stephen O'Connor

Acting Assistant Professor

University of Washington

Eligibility Criteria

Inclusion Criteria

  • at least 15 years of age
  • Inpatient on medical/surgical unit
  • Admitted following a suicide attempt
  • Sufficient English to benefit from psychotherapy in English
  • Consents to be a research participant

Exclusion Criteria

  • Lack of sufficient English to participate in psychotherapy in English
  • Prisoner/inmate at time of admission
  • Too cognitively impaired, delirious, or psychotic to respond to psychotherapeutic intervention before end of stay on medical/surgical unit. Determination of cognitive impairment, delirium, agitation, and psychosis will be determined through the referral phone call between the PI and the referring care provider, as well as the PI's own clinical assessment of the patient at the outset of the brief intervention.

Outcomes

Primary Outcomes

Patient Satisfaction Questionnaire

Time Frame: (baseline) Assessment taking place immediately after completion of intervention

The Patient Satisfaction Questionnaire will be used to determine the acceptability of the intervention by the patient.

Secondary Outcomes

  • Scale for Suicide Ideation(One month follow-up assessment)

Study Sites (1)

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