A Novel Peer-Delivered Recovery-Focused Suicide Prevention Intervention for Veterans With Serious Mental Illness

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVA Office of Research and Development

About this trial

Suicide is a major public health concern, particularly among Veterans with serious mental illness (SMI, i.e., psychotic disorders or bipolar disorders). Wellness Recovery Action Plan (WRAP) is a well-established evidence-based practice for those with SMI that centers on identifying warning signs of mental illness, developing wellness tools for functional independence, planning for day-to-day effective living within one's community, and building an action plan to create a valued life worth living. This proposed study will refine and pilot SUicide Prevention by Peers Offering Recovery Tactics (SUPPORT), a novel integrated recovery program that is an adaptation of peer-delivered WRAP for Veterans with SMI. In SUPPORT, a Peer Specialist leads a Veteran at increased risk for suicide through recovery planning that is tailored to the Veteran's suicidal experiences with cognitive learning strategies to enhance safety plan recall and improve functioning.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Veterans who report present suicidal ideation (i.e., Columbia-Suicide Severity Rating Scale (C-SSRS) > 2 ("Active thoughts of killing oneself") in past 1 month and/or a suicide attempt in the prior 3 months as identified by the C-SSRS

Current SMI diagnosis (i.e., schizophrenia and other psychotic disorders, mood disorders with psychotic features, bipolar disorders)

Capable of informed consent via the University of California San Diego Brief Assessment of Capacity to Consent (UBACC)

Certified Peer Specialist employed at VA San Diego Healthcare System (VASDHS) in the Mental Health Care Line (individuals must demonstrate competency in basic suicide screening and referral procedures to be certified)

Disqualifiers

Cannot complete the assessment battery

Current intoxication requiring immediate detoxification or outpatient plan directed specifically to residential substance use disorder (not mental health) services

Imminent psychiatric hospitalization

Trial design

Design model

Parallel

Treatments tested in this trial

  • SUicide Prevention by Peers Offering Recovery Tactics

    Behavioral

    Following the completion of a comprehensive mental health evaluation by a licensed VA provider, which includes a suicide safety plan, if a Veteran is having active thoughts of suicide or made a suicide attempt in past three months, they may be eligible for SUPPORT. In SUPPORT, the Peer Specialist and Veteran co-create a personalized suicide-focused recovery plan (SUPPORT Plan) in flexible, 50-minute weekly encounters. The SUPPORT Plan includes modules that focus on valuing recovery, building a hope kit and daily plan, setting recovery goals, and looking ahead to enhance the Veteran's safety plan. Learning strategies are incorporated into each module to promote salience and recall of intervention material. The Peer Specialist works closely with the Veteran's treatment team and uses the most recent safety plan in the Veteran's chart to help complete the SUPPORT Plan as well as reinforce the usage of the Veteran's safety plan.

Treatment groups

69 Participants
are divided into 2 treatment groups
Group A: SUPPORTExperimental treatment 1 intervention
Group B: ESCNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Feasibility of recruitment and retention

Recruitment and retention is determined by the number of participants who were initially contacted, consented, completed baseline data, and completed follow-up data.

Time frame
Through study completion, an average of 4 years
2

Acceptability of SUPPORT as measured by the Client Satisfaction Questionnaire-8 (CSQ-8)

The CSQ-8 brief survey has been used extensively in VA and non-VA settings to assess overall satisfaction with care, and it has excellent internal consistency (0.93). An overall score" is calculated by summing the participant's rating score for each scale item. Scores range from 8 to 32, with higher values indicating higher satisfaction.

Time frame
At the end of the intervention, an average of 4-weeks

Secondary outcomes

1

Change in the Scale for Suicide Ideation (SSI)

The SSI is an 19-item interviewer administered assessment of suicidal ideation (SI) severity. The total score ranges from 0 to 38 with higher scores indicating more serve SI. The scale has demonstrated strong validity and reliability.

Time frame
Baseline, 2-weeks, 4-weeks, 3-month follow-up
2

Change in Recovery Assessment Scale-41

The RAS-41 is a self-report measure of personal recovery with five domains: personal confidence and hope; willingness to ask for help; goal and success orientation; reliance on others; no domination by symptoms. A review study found high Cronbach's alphas (.76 and .97) and test-retest reliability (.65 to .88). The RAS has been widely used in VA and non-VA clinical trial studies with diverse populations, a range of mental illnesses, and has demonstrated sensitivity to change over time.

Time frame
Baseline, 2-weeks, 4-weeks, 3-month follow-up

Other outcomes

Sponsors and contacts

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