Actively Recruiting

Phase Not Applicable
Age: 12Years - 17Years
All Genders
Healthy Volunteers
NCT07197476

Adolescent Stress and Substance Intervention Subsequent to Trauma

Led by Rhode Island Hospital · Updated on 2026-04-28

92

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

Sponsors

R

Rhode Island Hospital

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The long-term goal of this study is to address the adoption of the new trauma center requirement to establish best practices of screening for acute stress with an intervention to prevent both adolescent PTSD and substance use. The investigators will develop, refine, and pilot test the Adolescent Stress and Substance Intervention Subsequent to Trauma (ASSIST) video interventions that build upon the American College of Surgeons Committee on Trauma guidelines to improve mental health care during and after hospitalization for traumatic injury. The aims are: PHASE I - Primary Aim 1: To develop and refine two ASSIST video interventions for adolescents and parents admitted to a level 1 pediatric trauma center. PHASE II * Primary Aim 2a: To evaluate the feasibility, acceptability and implementation potential of the ASSIST video interventions. * Primary Aim 2b: Develop the ASSIST implementation protocol using a national advisory panel of pediatric trauma center leaders. Participants in PHASE 1: Parent and child duo: * Review storyboards for the video interventions * Participate in qualitative interviews at hospital admission and 1 month following discharge Pediatric trauma center clinical staff members: \- Complete qualitative interviews Participants in PHASE II: Parent and child duo: * Shown their own video interventions * Complete assessments at admission and 1-, 2-, 3- months after discharge

CONDITIONS

Official Title

Adolescent Stress and Substance Intervention Subsequent to Trauma

Who Can Participate

Age: 12Years - 17Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth aged 12 to 17 years
  • Fluent in English or Spanish
  • Able to provide informed assent
  • Has a parent or guardian able to provide informed consent
  • Parent or guardian lives with the admitted pediatric trauma patient
  • Parent or guardian fluent in English or Spanish
  • Parent or guardian able to provide informed consent
Not Eligible

You will not qualify if you...

  • Prisoner or in police custody
  • Involvement with child protective services
  • Admission due to suicide attempt or non-suicidal self-injury
  • Any acute condition preventing informed consent or assent

AI-Screening

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Trial Site Locations

Total: 1 location

1

Rhode Island Hospital

Providence, Rhode Island, United States, 02903

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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