Adapting a Brief Suicide Intervention for Pediatric Primary Care: Enhancing Uptake and Impact

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age10+
SponsorUniversity of Washington

About this trial

Suicide is a leading cause of death among adolescents in the United States and improving access to high quality just-in-time suicide interventions to reduce risk has important public health implications. Integrating such interventions into routinely accessed settings, such as pediatric primary care, holds promise; however, many clinicians in these settings fail to adequately screen or intervene in youth suicidal thoughts and behaviors, representing a key barrier to reducing suicide. The proposed study is a pre-post quasi-experimental pilot feasibility and preliminary efficacy trial of a suicide prevention intervention informed by evidence based interventions including the SAFETY-Acute suicide prevention intervention implemented in 3 pediatric primary care clinics.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

adolescent between the ages of 10 and 18 years old

speaks fluent English

current or recent suicide risk

Disqualifiers

high suicide risk (in need of immediate crisis stabilization services such as inpatient medical or psychiatric hospitalization)

does not speak fluent English

does not have a primary care provider

has a child who meets inclusion criteria

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pilot Intervention

    Behavioral

    This intervention is a suicide prevention intervention that will be adapted from evidence-based suicide prevention interventions including the SAFETY-Acute program. The specific intervention components will be determined from information gathered in this study but the investigators anticipate will include components such as identifying strengths, coping skills, safety planning, lethal means restriction, psychoeducation, motivation building, and care linkage.

  • Treatment as Usual

    Behavioral

    Treatment as usual delivered in participating clinics.

Treatment groups

48 Participants
are divided into 2 treatment groups
Group A: Treatment as usualActive comparator 1 intervention
Group B: Pilot InterventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility of Intervention Measure

Feasibility of the intervention (includes 4 items scored on a 5 point likert scale with higher scores representing greater feasibility.)

Time frame
Participant and providers complete approximately 2 weeks after completing intervention
2

Acceptability of Intervention Measure

Participant rated acceptability of the intervention (includes 4 items scored on a 5 point likert scale with higher scores representing greater acceptability.)

Time frame
Participant and providers complete approximately 2 weeks after completing intervention
3

Intervention Appropriateness Measure

Participant rated appropriateness of the intervention (includes 4 items scored on a 5 point likert scale with higher scores representing greater appropriateness.)

Time frame
Participant and providers complete approximately 2 weeks after completing intervention
4

Client Satisfaction Questionnaire

Participant rated satisfaction with the intervention (includes 8 items scored on a 4 point likert scale with higher scores representing greater satisfaction.)

Time frame
Participant completes approximately 2 weeks after completing intervention

Secondary outcomes

1

Parent Self Efficacy Scale

Caregiver rated self-efficacy of being able to keep youth safe (includes 5 items scored on a 5 point likert scale with greater total score representing greater parent self-efficacy).

Time frame
Participant completes at baseline, approximately 2 weeks after completing intervention, and again 2 months following the intervention
2

Adapted General Self-Efficacy Scale

Patient rated self-efficacy of being able to keep self safe (includes 10 items scored on a 4 point likert scale with greater total score representing greater self-efficacy).

Time frame
Participant completes at baseline, approximately 2 weeks after completing intervention, and again 2 months following the intervention
3

Adult Child Relationship Scale (ACRS)/Child Parent Relationship Scale (CPRS)

Patient and caregiver rated family involvement/relationship quality (includes 19 items scored on a 5 point likert scale with two subscales \[closeness and conflict\] where higher total score on each subscale represents greater closeness or conflict).

Time frame
Participant completes at baseline, approximately 2 weeks after completing intervention, and again 2 months following the intervention

Other outcomes

1

Ask Suicide Screening Questions (ASQ)

Exploratory suicide and mental health outcomes (includes 5 items scored as yes/no with greater number of yes or a yes on item 5 representing greater suicide risk).

Time frame
Participant completes at baseline, approximately 2 weeks after completing intervention, and again 2 months following the intervention
2

Revised Children's Anxiety and Depression Scale-25

Exploratory suicide and mental health outcomes (includes 25 items scored on a 4 point likert scale with higher total score representing greater symptom severity).

Time frame
Participant completes at baseline, approximately 2 weeks after completing intervention, and again 2 months following the intervention
3

Diagnostic and Statistical Manual of Mental Disorders-5 cross cutting assessment

Exploratory suicide and mental health outcomes (includes 25 items scored on a 4 point likert scale with higher scores representing greater symptom severity).

Time frame
Participant completes at baseline, approximately 2 weeks after completing intervention, and again 2 months following the intervention

Sponsors and contacts

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University of Washington

Lead sponsor

National Institute of Mental Health (NIMH)

Collaborator