Peer Mentorship to Reduce Suicide Risk Following Psychiatric Hospitalization

Not Applicable

Completed

• Conditions: Suicidal Ideation

• Registration Number: NCT02365116
• Lead Sponsor: University of Michigan

Brief Summary

Every year in the United States about 1 million people make a suicide attempt and more than 38,000 die by suicide. The risk of suicide is highest among individuals with mental illness who have been hospitalized due to suicidal thoughts or behaviors, yet there are few interventions known to reduce suicide risk in this population. This study will develop and pilot test a peer mentorship intervention by which trained peer professionals will use their own personal experience with recovery from mental illness to instill hope and belongingness in high-risk patients and provide additional support to prevent future suicidal thoughts or behaviors.

The specific aims of the study are to: (1) develop a peer mentorship intervention to reduce suicide risk among patients psychiatrically hospitalized with suicidal ideation or following a suicide attempt; (2) Conduct a randomized controlled pilot study to assess the acceptability, feasibility, and fidelity of the peer mentorship intervention in preparation for a larger efficacy trial; and (3) an exploratory aim will be to measure potential mediators and moderators of intervention effectiveness in terms of belongingness, burdensomeness, and hopelessness according to the interpersonal theory of suicide.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2014-05-28
• Study First Submitted QC: 2015-02-17
• Study First Posted: 2015-02-18
• Study Start: 2015-08-19
• Primary Completion: 2017-05-26
• Study Completion: 2017-05-26
• Status Verified: 2017-08
• Last Update Submitted: 2017-08-11
• Last Update Posted: 2017-08-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 79

Inclusion Criteria

1. are age 18 years or older
2. have medical record documentation of suicidal ideation or suicide attempt at the time of admission
3. are fluent in English

Exclusion Criteria

1. substantially cognitively impaired (according to Mini-Cog)
2. unable to provide voluntary, written, informed consent for any reason (including incompetency)
3. determined by the patient's attending psychiatrist that due to the patient's psychiatric condition peer mentorship may be harmful to the patient or peer specialist (e.g., severe personality disorder, unstable paranoia)
4. already receiving or intending to receive peer mentorship (including having a sponsor from Alcoholics Anonymous) or participate in group-based peer support on a biweekly or more frequent basis
5. are receiving electroconvulsive therapy (ECT)
6. are located more than 50 miles from any of the peer specialists
7. are being discharged to a residential treatment facility

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Intervention feasibility (Study team's ability to deliver the intervention)	3 and 6 months post-baseline	Study team's ability to deliver the intervention as a measure of feasibility. Measured by at least 50% of eligible patients choosing to enroll in the study, at least 80% of participants assigned to the peer mentorship arm meeting with a peer specialist prior to hospital discharge, at least 70% of participants in both study arms completing follow-up measures at 6 months, and the study meeting its enrollment goal of 60 patients in 12 months.
Intervention acceptability (median number of peer mentorship contacts at 3 months post-discharge is at least 4, as well as by satisfaction questionnaires.)	3 and 6 months post-baseline	Patients' willingness and satisfaction with participating in the intervention as a measure of intervention acceptability. Measured by at least 70% of participants in both study arms completing follow-up measures at 6 months, the median number of peer mentorship contacts at 3 months post-discharge is at least 4, as well as by satisfaction questionnaires.

Secondary Outcome Measures

Name	Time	Method
Current suicidal ideation (measured by the Beck Suicide Scale (BSS)	3 and 6 months post-baseline	Patient's current suicidal ideation as measured by the Beck Suicide Scale (BSS)
Peak suicidal ideation (measured by the Columbia Suicide Severity Rating Scale (CSSR-S)	3 and 6 months post-baseline	Patient's peak suicidal ideation since the last visit as measured by the Columbia Suicide Severity Rating Scale (CSSR-S)
Suicide attempts (measured by the Columbia Suicide Severity Rating Scale)	3 and 6 months post-baseline	Patient's suicide attempts since the last visit as measured by the Columbia Suicide Severity Rating Scale

Trial Locations

Locations (2)

University of Michigan Inpatient Psychiatry Unit; 🇺🇸 Ann Arbor, Michigan, United States

Henry Ford Kingswood Hospital; 🇺🇸 Ferndale, Michigan, United States