Actively Recruiting

Phase Not Applicable
Age: 12Years - 17Years
All Genders
ID07150832

I-CARE: Efficacy of a Digital Health Intervention to Reduce Suicidal Ideation During Psychiatric Boarding in Adolescents

Led by Dartmouth-Hitchcock Medical Center · Updated on 2025-10-31

173

Participants Needed

4

Research Sites

N/A

Total Duration

On this page

Sponsors

D

Dartmouth-Hitchcock Medical Center

Lead Sponsor

Y

Yale University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effectiveness of I-CARE, a digital health program designed to support adolescents aged 12 to 17 who experience suicidal thoughts, suicide attempts, or self-harm and are awaiting psychiatric hospitalization in emergency departments. This study addresses the challenge of psychiatric boarding, where youth remain in the emergency department while waiting for a psychiatric inpatient bed, a vulnerable time with little research on supportive interventions. The trial compares I-CARE against standard safety supervision to determine if it can improve care quality during boarding. I-CARE is a tablet-based program featuring seven web-based animated videos and workbook exercises that teach evidence-based psychosocial skills grounded in cognitive behavioral therapy and dialectical behavior therapy. The program is facilitated by trained staff who are not mental health professionals and is delivered alongside usual one-on-one safety supervision during boarding. Participants are randomized to either receive I-CARE in addition to standard safety supervision or standard safety supervision alone. Participants will be assessed at multiple points: at hospital admission, discharge (about 72 hours after admission), and then 30, 60, and 90 days after discharge. Researchers will use standardized questionnaires to measure depression, anxiety, stress, suicidal risk, and suicidal behaviors. The study includes ongoing monitoring and data collection over these time points to evaluate the impact of the intervention on youth mental health during and after psychiatric boarding.

CONDITIONS

Brief Title

Efficacy of the I-CARE Digital Health Intervention

Who Can Participate

Age: 12Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescents aged 12 to 17 years at emergency department visit or hospital encounter
  • Presenting with suicide attempt, suicidal ideation, or self-harm
  • Medically stable condition
  • English-speaking
  • Awaiting transfer for inpatient psychiatric care or disposition
Not Eligible

You will not qualify if you...

  • Cognitive or developmental delays that prevent participation (intellectual functioning below 12 years of age)
  • Behavioral limitations that prevent program participation
  • Active psychosis
  • Legal parent or caregiver unable to speak English or unavailable to provide consent (e.g., wards of the state)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Inpatient Treatment

Duration - Approximately 72 hours or duration of psychiatric boarding

Participants receive the I-CARE digital intervention consisting of 7 tablet-based animated video modules and workbook exercises during psychiatric boarding while awaiting transfer to inpatient psychiatric care.

1 baseline visit during boarding

Follow-up

Duration - 90 days post-discharge

Participants are monitored for mental health outcomes after discharge from the hospital to assess the effects of the intervention.

Visits approximately at 30, 60, and 90 days post-discharge

Trial Site Locations

Total: 4 locations

1

Yale

New Haven, Connecticut, United States, 06520

Actively Recruiting

2

Dartmouth College

Hanover, New Hampshire, United States, 03755

Not Yet Recruiting

3

Dartmouth Health

Lebanon, New Hampshire, United States, 03756

Not Yet Recruiting

4

Weill Cornell Medicine

New York, New York, United States, 10065

Actively Recruiting

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Research Team

S

Stephanie C. Acquilano, MA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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