Pilot Study of a Brief Intervention for Medically Hospitalized Suicide Attempt Survivors
1 other identifier
interventional
69
1 country
1
Brief Summary
The current study proposes to study the feasibility and acceptability of a brief psychosocial intervention delivered to suicide attempt survivors hospitalized on a medical/surgical floor or inpatient psychiatry unit at Vanderbilt University Medical Center. The proposed study will involve training of care providers affiliated with Vanderbilt University Medical Center to deliver the brief intervention. Additionally, the participants will complete baseline, 1, 3, and 12-month assessments on outcomes of interest, including readiness to change problematic behaviors, engagement in outpatient mental health services, suicidal ideation, self-harming behavior, and reasons for living.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_1
Started Jul 2014
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2014
CompletedFirst Submitted
Initial submission to the registry
December 16, 2014
CompletedFirst Posted
Study publicly available on registry
April 13, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 14, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
June 14, 2017
CompletedMay 3, 2018
May 1, 2018
3 years
December 16, 2014
May 2, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Client Satisfaction Questionnaire
The 8-item Client Satisfaction Questionnaire is a general measure of individual satisfaction with health and human services that takes 3-8 minutes to complete.
Immediately following Brief Intervention
Secondary Outcomes (6)
Change in Stages of Change Questionnaire
Baseline, 1-, 3-, and 12-months interviews
Change in Scale for Suicide Ideation
Baseline, 1-, 3-, and 12-months interviews
Change in Suicide Attempt Self-Injury Count
Baseline, 1-, 3-, and 12-months interviews
Change in Interpersonal Needs Questionnaire
Baseline, 1-, 3-, and 12-months interviews
Change in Reasons for Living Inventory
Baseline, 1-, 3-, and 12-months interviews
- +1 more secondary outcomes
Study Arms (2)
Care as Usual
NO INTERVENTIONParticipants will receive usual care services provided to suicide attempt survivors, including inpatient psychiatry, outpatient psychotherapy, and case management.
Teachable Moment Brief Intervention
EXPERIMENTALThe 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, functional analysis of the suicidal ideation and behaviors, and crisis response planning. Participants will also receive usual care services provided to suicide attempt survivors, including inpatient psychiatry, outpatient psychotherapy, and case management.
Interventions
functional analysis, collaborative interpersonal style
Eligibility Criteria
You may qualify if:
- years of age and above
- Inpatient on medical/surgical unit either currently or prior to transfer to inpatient psychiatric unit
- Admitted following a suicide attempt
- Sufficient English to benefit from psychotherapy in English
- Consents to be a research participant
You may not qualify if:
- 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 in the medical center. Determination of cognitive impairment, delirium, agitation, and psychosis will be determined through the referral phone call between discussions with research team members and the Adult Psychiatry Consultation Service Physician providing care to the patient, as well as the interventionist's own clinical assessment of the patient at the outset of the brief intervention.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Western Kentucky Universitylead
- Vanderbilt Universitycollaborator
Study Sites (1)
Vanderbilt University Medical Center
Nashville, Tennessee, 37232, United States
Related Publications (2)
Witt KG, Hetrick SE, Rajaram G, Hazell P, Taylor Salisbury TL, Townsend E, Hawton K. Psychosocial interventions for self-harm in adults. Cochrane Database Syst Rev. 2021 Apr 22;4(4):CD013668. doi: 10.1002/14651858.CD013668.pub2.
PMID: 33884617DERIVEDO'Connor SS, Mcclay MM, Choudhry S, Shields AD, Carlson R, Alonso Y, Lavin K, Venanzi L, Comtois KA, Wilson JE, Nicolson SE. Pilot randomized clinical trial of the Teachable Moment Brief Intervention for hospitalized suicide attempt survivors. Gen Hosp Psychiatry. 2020 Mar-Apr;63:111-118. doi: 10.1016/j.genhosppsych.2018.08.001. Epub 2018 Aug 10.
PMID: 30389316DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Stephen S O'Connor, Ph.D.
Western Kentucky University
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 16, 2014
First Posted
April 13, 2015
Study Start
July 1, 2014
Primary Completion
June 14, 2017
Study Completion
June 14, 2017
Last Updated
May 3, 2018
Record last verified: 2018-05