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Improving Screening and Follow Up for Suicidal Ideation and Behaviors Among Latinx Youth in Primary Care

Not Applicable
Recruiting
Conditions
Suicidal Ideation
Interventions
Behavioral: PALOMA
Registration Number
NCT06229223
Lead Sponsor
Johns Hopkins University
Brief Summary

The objective of this proposal is to develop and pilot a systems-level strategy in pediatric primary care to enhance identification and management of suicidal ideation and behavior in Latinx youth, particularly those in immigrant families with parents who have limited English proficiency (LEP). The investigators will focus on the use of trained community health workers (CHWs) to increase clinic capacity and quality of suicide risk screening and early intervention, with a focus on safety planning, parent psychoeducation and care coordination.

Specific aims are 1: To develop site-specific implementation protocols for the integration of CHWs into SIB screening and safety planning for Latinx youth and the youths families; 2: To pilot the implementation of the program in a six-month open trial in four pediatric primary care practices representing a range of usual practice settings; and 3: To engage a stakeholder network to explore barriers and facilitators, including costs and billing strategies, to implementation of this approach across a broad range of pediatric primary care settings.

Parents/guardians of youth who have been referred to and agree to participate in the intervention by the child's primary care provider will participate in a 2-month program consisting of 6-8 phone sessions with a community health worker focusing on safety planning, information/education, program solving and self-care. Research participants will be asked to complete a survey via phone at the beginning of the program and another at the end of the program. The participants may also be asked to participate in an additional interview about the study.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
250
Inclusion Criteria
  • Youth has history of suicidal ideation/behavior or non-suicidal self-harm and
  • Youth identifies as Latino/Latinx/Hispanic/Latin American and
  • Guardian(s) speaks Spanish
Exclusion Criteria
  • None

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
PALOMAPALOMAParents/guardians of youth who have been referred to and agree to participate in the intervention by the child's primary care provider will participate in a 2-month program consisting of 5-7 phone sessions with a community health worker focusing on safety planning, information/education, program solving and self-care. Research participants will be asked to complete a survey via phone at the beginning of the program and another at the end of the program. The participants may also be asked to participate in an additional interview about the participants experience during the study.
Primary Outcome Measures
NameTimeMethod
Percent of Participants ScreenedMonthly for 9 months

Percent of patients 10-18 years old screened for depression and suicidal ideation and behavior at clinic level

Feasibility as assessed by percent of sessions completedMonthly for 9 months

Percent of eligible patients receiving a CHW session

Quality as assessed by percent of CHW visitsMonthly for 9 months

Percent of CHW visits that include delivery of one or more intervention components

Engagement as assessed by number of follow-up visitsMonthly for 9 months

number of follow-up mental health visits with PCP or specialty provider among youth identified as having suicidal ideation or behavior.

Secondary Outcome Measures
NameTimeMethod
Family Functioning as assessed by the SCORE-15 Index of Family Functioning and Change (SCORE-15)Baseline and 3 months

SCORE-15 Index of Family Functioning and Change: Score range 5-15, higher total means worse functioning.

Parent Self Efficacy as assessed by Brief Parenting Self Efficacy Scale (BPSES) QuestionnaireBaseline and 3 months

Brief Parenting Self Efficacy Scale (BPSES) Questionnaire: Total score ranges from 5 to 25, higher scores indicate higher levels of parental self-efficacy.

Depression as assessed by the Patient Health Questionnaire - Adolescent (PHQ-A)Baseline and 3 months

Patient Health Questionnaire - Adolescent (PHQ-A): Each item on the PHQ-A is scored as follows: Not at all = 0 Several Days = 1 More than half the days = 2 Nearly every day = 3. A weighted score of 5 or more means a positive screen for depressive symptoms. A weighted score of 0-4 means a negative screen for depressive symptoms.

Suicidal Ideation and Behavior as assessed by the Ask Suicide-Screening Questionnaire (ASQ)Baseline and 3 months

Ask Suicide-Screening Questionnaire (ASQ): 4 Yes or No Questions. "Yes" to questions 1 through 4, or refuses to answer is considered a positive screen. "Yes" to question 5 = acute positive screen (imminent risk identified); "No" to question 5 = non-acute positive screen.

Parental Self-Efficacy to Support Teens During a Suicidal Crisis surveyBaseline and 3 months

9 items. Answer choices ranged from 0 (not at all confident) to 10 (completely confident), with an anchor of 5 (somewhat confident); score range 0-90; higher score higher confidence.

Parent expectations of adolescents' risk surveyBaseline and 3 months

3 items. Answer choices ranged from 0 (not at all confident) to 10 (completely confident), with an anchor of 5 (somewhat confident). Score range 0-30; higher score higher confidence.

Trial Locations

Locations (1)

BMS at Yard 56

🇺🇸

Baltimore, Maryland, United States

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