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Peer Mentorship to Reduce Suicide Risk Following Psychiatric Hospitalization

Primary Purpose

Suicidal Ideation

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Peer mentorship
Enhanced Usual Care
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Suicidal Ideation focused on measuring Peer Mentorship, Psychiatric Hospitalization, Suicide Risk

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University of Michigan Inpatient Psychiatry Unit
  • Henry Ford Kingswood Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Peer Mentorship intervention

Enhanced Usual Care

Arm Description

A Peer Specialist will be making weekly follow-up contact with study participants in the community or by telephone for 3 months following hospital discharge. The content of the peer mentorship interactions will be based on the manual developed by the study team and will include components such as hope and belongingness.

Patients will continue to receive usual care which typically consists of referral to an outpatient psychiatrist. Participants will also receive a phone call within 24-72 hours from a member of the inpatient unit clinical staff to assess barriers to follow-up care and safety. The enhancement to usual care will occur at the 3 and 6 month follow-up assessments, where participants will be assessed to determine whether they require any additional referral information for follow-up care. If referral information is indicated, the patient will be provided a list of mental health treatment providers in their area.

Outcomes

Primary Outcome Measures

Intervention acceptability (median number of peer mentorship contacts at 3 months post-discharge is at least 4, as well as by satisfaction questionnaires.)
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.
Intervention feasibility (Study team's ability to deliver the intervention)
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.

Secondary Outcome Measures

Current suicidal ideation (measured by the Beck Suicide Scale (BSS)
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)
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)
Patient's suicide attempts since the last visit as measured by the Columbia Suicide Severity Rating Scale

Full Information

First Posted
May 28, 2014
Last Updated
August 11, 2017
Sponsor
University of Michigan
Collaborators
National Institutes of Health (NIH)
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1. Study Identification

Unique Protocol Identification Number
NCT02365116
Brief Title
Peer Mentorship to Reduce Suicide Risk Following Psychiatric Hospitalization
Official Title
Peer Mentorship to Reduce Suicide Risk Following Psychiatric Hospitalization
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
August 19, 2015 (Actual)
Primary Completion Date
May 26, 2017 (Actual)
Study Completion Date
May 26, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Institutes of Health (NIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicidal Ideation
Keywords
Peer Mentorship, Psychiatric Hospitalization, Suicide Risk

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
79 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Peer Mentorship intervention
Arm Type
Experimental
Arm Description
A Peer Specialist will be making weekly follow-up contact with study participants in the community or by telephone for 3 months following hospital discharge. The content of the peer mentorship interactions will be based on the manual developed by the study team and will include components such as hope and belongingness.
Arm Title
Enhanced Usual Care
Arm Type
Active Comparator
Arm Description
Patients will continue to receive usual care which typically consists of referral to an outpatient psychiatrist. Participants will also receive a phone call within 24-72 hours from a member of the inpatient unit clinical staff to assess barriers to follow-up care and safety. The enhancement to usual care will occur at the 3 and 6 month follow-up assessments, where participants will be assessed to determine whether they require any additional referral information for follow-up care. If referral information is indicated, the patient will be provided a list of mental health treatment providers in their area.
Intervention Type
Behavioral
Intervention Name(s)
Peer mentorship
Intervention Description
Patients who are working with a peer specialist will have their sessions audio taped and reviewed by research staff for training purposes and to ensure that peer specialists are following protocol.
Intervention Type
Behavioral
Intervention Name(s)
Enhanced Usual Care
Intervention Description
The enhancement to usual care will occur at the 3 and 6 month follow-up assessments, where participants will be assessed to determine whether they require any additional referral information for follow-up care. If referral information is indicated, the patient will be provided a list of mental health treatment providers in their area.
Primary Outcome Measure Information:
Title
Intervention acceptability (median number of peer mentorship contacts at 3 months post-discharge is at least 4, as well as by satisfaction questionnaires.)
Description
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.
Time Frame
3 and 6 months post-baseline
Title
Intervention feasibility (Study team's ability to deliver the intervention)
Description
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.
Time Frame
3 and 6 months post-baseline
Secondary Outcome Measure Information:
Title
Current suicidal ideation (measured by the Beck Suicide Scale (BSS)
Description
Patient's current suicidal ideation as measured by the Beck Suicide Scale (BSS)
Time Frame
3 and 6 months post-baseline
Title
Peak suicidal ideation (measured by the Columbia Suicide Severity Rating Scale (CSSR-S)
Description
Patient's peak suicidal ideation since the last visit as measured by the Columbia Suicide Severity Rating Scale (CSSR-S)
Time Frame
3 and 6 months post-baseline
Title
Suicide attempts (measured by the Columbia Suicide Severity Rating Scale)
Description
Patient's suicide attempts since the last visit as measured by the Columbia Suicide Severity Rating Scale
Time Frame
3 and 6 months post-baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: are age 18 years or older have medical record documentation of suicidal ideation or suicide attempt at the time of admission are fluent in English Exclusion Criteria: substantially cognitively impaired (according to Mini-Cog) unable to provide voluntary, written, informed consent for any reason (including incompetency) 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) 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 are receiving electroconvulsive therapy (ECT) are located more than 50 miles from any of the peer specialists are being discharged to a residential treatment facility
Facility Information:
Facility Name
University of Michigan Inpatient Psychiatry Unit
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Name
Henry Ford Kingswood Hospital
City
Ferndale
State/Province
Michigan
ZIP/Postal Code
48220
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Peer Mentorship to Reduce Suicide Risk Following Psychiatric Hospitalization

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