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N/A N=17 Health Services Research

Peer Based Suicide Prevention

Suicide

Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Apr 2025
Primary outcome: Primary: Questionnaire About the Process of Recovery (QPR) Change — 48.3; 50.1 score on a scale — p=.05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Peer Specialist Suicide Prevention (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Dec 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Questionnaire About the Process of Recovery (QPR) Change
48.3; 50.1 .05
PRIMARY
Hearth Hope Index
27.5; 29.2 .05
PRIMARY
Suicide Cognitions Scale (SCS) Change
38.8; 36.3 .05
PRIMARY
Interpersonal Needs Questionnaire (INQ) Change - Perceived Burden
20.7; 20.3 .05
PRIMARY
Interpersonal Needs Questionnaire (INQ) Change - Thwarted Belonging
37.3; 41.1 .05
PRIMARY
Quick Inventory of Depressive Symptoms (QIDS) Change
19.4; 17.3 .05
PRIMARY
Columbia-Suicide Severity Rating Scale (C-SSRS) - Suicidal Ideation
2.67; 1.08 .05
PRIMARY
Columbia-Suicide Severity Rating Scale (C-SSRS) - Suicidal Ideation Intensity
11.8; 9.42 .05

Summary

Veterans Health Administration (VHA) suicide rates remain high, requiring new approaches. VHA patients tend to have high medical and behavioral health care needs that cause disruption in their lives and heighten their risk of suicide. This study will adapt and pilot test an intervention that expands the focus of care for VHA patients with high risk for suicide to building a life of self-respect, meaning, and connectedness in one's local community. The pilot intervention will involve receiving support and mentorship from a fellow Veteran living with the same challenges who has been trained in helping others manage their disabilities while achieving specific life goals (i.e., a 'Peer Specialist'). Results from this study will demonstrate the preliminary effectiveness of supplementing the VHA's current clinical approaches to suicide prevention with support provided by a trained Peer Specialist that offers empathy, hope, and practical advice that stemming from 'lived experience' of disability and recovery.

Eligibility Criteria

Inclusion Criteria

  • The investigators will target Veterans with suicide flags because they are at greatest risk for suicide and therefore most in need of intervention
  • Eligibility will be limited to Veterans diagnosed with unipolar or bipolar depression as this diagnostic group is the most prevalent in suicidal samples and is supported by prior meta-analyses on peer-provided interventions
  • The investigators will ensure decision-making capacity using the Blessed Orientation, Memory, Concentration Test and a brief quiz about the study
  • This quiz will involve an iterative process of querying the participants' understanding of consent information with a 10-item true/false test and providing feedback until an acceptable level of understanding is achieved (must get 100% correct after 3 tries to enroll)

Exclusion Criteria

  • cognitive impairment as indicated by a Blessed score of >10
  • unable to provide voluntary, written informed consent for any reason
  • e.g., incompetency
  • determination by the patient's psychiatrist not to be appropriate for participation due to unstable psychosis, cognitive disorder, or severe personality disorder
  • residing more than 50 miles away
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04222673). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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