This study will determine if suicidal middle-aged men who use a personalized computer program addressing suicide risk before a primary care visit are more likely to discuss suicide and accept treatment, reducing their suicide preparatory behaviors and thoughts.This is important because half of all men who die by suicide visit primary care within a month of death, yet few broach the topic, missing chances for prevention.
In this study, the investigators will enroll middle-aged men with active suicide thoughts in a randomized controlled trial (RCT) to examine whether their use of the Men and Providers Preventing Suicide (MAPS) tailored interactive multimedia patient activation program immediately before a primary care provider (PCP) visit, linked with integrated telephone evidence-based follow-up care (TEBFC) (vs. attention control exposure linked with TEBFC), reduces suicide preparatory behaviors and ideation over 3 months. About half of all middle-aged men who die by suicide are seen by a PCP within a month of dying, suggesting the value of primary care-based suicide prevention efforts, to complement strategies in other settings. Current impediments to primary care-based prevention are that many suicidal middle-aged men do not visit a PCP, and among those who do the topic of suicide is rarely broached, due to societal gender-linked norms (e.g., toughness); stigma; spurious concerns that talking about suicide increases risk; competing time demands; and lack of resources to cope with positive responses. PCP-targeted educational interventions have increased detection of suicidal men, but have inconsistently affected suicide behaviors, and still many suicidal men went undetected. Suicide behaviors are more likely to be reduced by evidence-based follow-up care - supportive follow-up contact and collaborative mental health care. However, such care can only be effective if at-risk men visit a PCP who identifies suicide risk and offers the care, and the men accept it. Thus, there is a pressing need to study the use of innovative tools like MAPS to activate at risk middle-aged men to signal their receptiveness to suicide discussion and care, prompting PCP inquiry and referrals to a form of follow-up care that is feasible for most practices to implement (e.g., TEBFC).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
93
3 minute video on sleep hygiene produced by HealthiNation
3 months of suicide-focused collaborative mental health care, directed by a supervising psychiatrist and implemented by a care manager working with the patient and their primary care provider
Palo Alto Medical Foundation Research Institute
Palo Alto, California, United States
University of California Davis Health System
Sacramento, California, United States
Patient: Beck Scale for Suicide Ideation
Time frame: 3 months
Patient: Reported discussion of suicide during study visits
Time frame: Immediately post-study visit
Patient: suicidal intent scale
Time frame: 3 months
Patient: enrollment in telephone evidence-based follow-up care
Time frame: Immediately post-study visit, 1 month, 2 months, 3 months
Patient adherence to telephone evidence-based follow-up care, ascertained from care manager patient contact logs
Time frame: 1 month, 2 months, 3 months
Patient: Interpersonal Needs Questionnaire
Perceived burdensomeness and belongingness to others
Time frame: 1 month, 2 months, 3 months
Patient: augmented Patient Health Questionnaire (PHQ-9)
PHQ-9 plus six "male depression" items
Time frame: 1 month, 2 months, 3 months
Patient: Short Form-12 health survey (SF-12) Mental Component Summary score
Mental health status
Time frame: 1 month, 2 months, 3 months
Patient: SF-12 Physical Component Summary score
Physical health status
Time frame: 1 month, 2 months, 3 months
Patient: Toughness scale
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Brief (30 minutes total time) video modules presenting participating patients' primary care providers with a patient-centered framework for suicide risk assessment and intervention
Gender-linked views regarding health-related help-seeking
Time frame: 1 month, 2 months, 3 months
Patient: perceptions of the study interventions and trial participation questionnaire
Time frame: 3 months
PCP: perceptions of baseline training videos questionnaire
Measured by questionnaire
Time frame: Immediately after completing the video training
PCP: reported discussion of suicide during study visits
Time frame: Immediately post-study visit
PCP: The number of times that PCPs refer study patients to TEBFC, ascertained from study care manager logs
Time frame: Through study completion, up to 3 years
PCP: attitudes toward caring for suicidal patients questionnaire
Time frame: At study completion, up to 3 years
PCP: perceptions of study participation questionnaire
Time frame: At study completion, up to 3 years