ClinicalTrials.Veeva

Menu

Peer Mentorship to Reduce Suicide Attempts Among High-Risk Adults (PREVAIL)

University of Michigan logo

University of Michigan

Status

Completed

Conditions

Suicidal Ideation

Treatments

Behavioral: Peer mentorship
Behavioral: Enhanced Usual Care

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03373916
1R01MH115111-01
HUM00137787

Details and patient eligibility

About

This is a single-blind, randomized controlled trial to test the effectiveness of a peer mentorship intervention (PREVAIL) for reducing suicide risk compared to enhanced usual care among participants (N=455) at high-risk for suicide recruited from inpatient psychiatric units.

Full description

Amid consistently worsening suicide rates, in 2012 the U.S. Surgeon General's National Strategy for Suicide Prevention proposed to "change the narrative" about suicide prevention to include a focus on promoting hope and belongingness. Despite hopelessness and thwarted belongingness being among the most replicated risk factors for suicide, many widely implemented suicide prevention efforts instead emphasize the identification of acute suicide risk and referral to mental health treatment services. However, there are very few health service interventions known to reduce suicides among those identified as high risk. Those interventions shown to be effective have not achieved the wide scale implementation necessary to alter the trend of increasing suicide deaths. New interventions are needed, and one promising, scalable intervention with a novel approach to addressing the risk factors advocated by the Surgeon General is peer mentorship. A peer mentorship intervention, PREVAIL, has been piloted in a two-site randomized controlled trial (N=70) and is acceptable and feasible with enrollment of nearly half of eligible high-risk patients, mean completion of over 6 mentorship sessions, and 85% of sessions meeting fidelity standards for addressing the intended targets of hope and belongingness.

The aims of this hybrid effectiveness-implementation study are:

Specific Aim 1: Determine the effectiveness of the PREVAIL peer mentorship intervention for reducing suicide attempts and suicidal ideation among recently hospitalized adult psychiatric patients at high risk for suicide.

Specific Aim 2: Examine the mechanisms of peer mentorship by measuring the effects of PREVAIL on potential mediators,including hope and belongingness.

Specific Aim 3: Identify barriers and facilitators to implementation of PREVAIL.

Enrollment

455 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. are age 18 years or older,
  2. are currently admitted to an inpatient psychiatric unit and have medical record documentation of suicidal ideation or suicide attempt at the time of admission,
  3. have a Beck Suicide Scale score of 5 or higher for the 1-week period prior to admission,
  4. are fluent in English,
  5. are able to be reached reliably by telephone.

Exclusion criteria

  1. substantially cognitively impaired (according to the Mini-Cog),
  2. unable to provide informed consent for any reason (including incompetency),
  3. determined by the patient's attending psychiatrist that peer mentorship is not appropriate due to unstable psychosis, cognitive disorder, or severe personality disorder,
  4. already receiving or intending to receive peer mentorship (i.e., sponsor from Alcoholics Anonymous) or group-based peer support on a biweekly or more frequent basis,
  5. residing more than 50 miles from any peer mentor,
  6. planning to be discharged to another inpatient or residential facility, or
  7. receiving electroconvulsive therapy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

455 participants in 2 patient groups

Peer Mentorship intervention (PREVAIL)
Experimental group
Description:
PREVAIL peer mentorship
Treatment:
Behavioral: Enhanced Usual Care
Behavioral: Peer mentorship
Enhanced Usual Care (EUC)
Active Comparator group
Description:
Enhanced Usual Care
Treatment:
Behavioral: Enhanced Usual Care

Trial documents
2

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems