MedPath

An Adaptive Intervention to Increase Engagement to Community-Based Care After an ED Admission

Not Applicable
Recruiting
Conditions
Suicidal and Self-injurious Behavior
Linkage to Care
Registration Number
NCT07092345
Lead Sponsor
Rhode Island Hospital
Brief Summary

The goal of this study is to develop a feasible brief, family-based adaptive intervention, via SMART design, for youth with suicidal and non-suicidal self-injurious behavior (SSIB) to increase community-based mental health (MH) care attendance and reduce SSIB risk post emergency department (ED) admission. The intervention will focus to increase understanding on youth MH literacy, MH communication, and MH engagement. Integrating an adaptive intervention via a SMART design in the ED could address subsequent barriers to youth obtaining appropriate level of community-based MH care and therefore reduce ED readmissions.

Detailed Description

This adaptive intervention allows for two stages of randomization to address treatment non-response. First, youth and caregivers (dyads) will be randomized to receive 1st-stage interventions in the ED, either the digital psychosocial-only condition or the psychosocial with digital health communication via text messages condition. If after two weeks, youth are identified as non-response, then dyads will be re-randomized to 2nd-stage intervention(s) that will include the use of a family navigation model.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
186
Inclusion Criteria
  • Youth 8 to 17 years
  • Youth presenting to the ED with suicide and self-injurious behavior
  • Youth living at home with at least one legal guardian/caregiver
Exclusion Criteria
  • Youth presenting to the ED with psychosis, sexual assault, child abuse
  • Youth in police custody,
  • Youth with an active investigation with the department of child and youth services (DCYF)
  • Youth unable to assent due to severity of illness or developmental disabilities,
  • Youth who cannot communicate in English or Spanish,
  • Youth without a caregiver/legal guardian who can provide consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Primary Outcome Measures
NameTimeMethod
Intervention Feasibility3-month & 6-month follow-up assessments

Recruitment rate (% of ppl who agree to be in the study), Study completion (% of ppl who complete entire study)

Child and Adolescent Service Assessment (CASA)3-month and 6-month follow-up assessments

Youth Attendance to Community-based Mental Health Care. CASA question and caregiver report of youth attendance in behavioral health care/community-based mental health services (yes or no) after discharge from emergency department admission.

Intervention Acceptability3-month and 6-month follow-up assessments

Client Satisfaction Questionnaire. An 8-item questionnaire that provides (positive \& negative) feedback from user opinion. Higher scores = greater satisfaction with intervention.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Hasbro Children's Hospital

🇺🇸

Providence, Rhode Island, United States

Hasbro Children's Hospital
🇺🇸Providence, Rhode Island, United States
Mary Kathryn Cancilliere, PhD
Contact
401-444-7443
marykathryn.cancilliere@brownhealth.org

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.