Reducing self-injurious thoughts and behaviors in adolescents during and after hospitalization
Official title: Therapeutic Evaluative Conditioning to Reduce Adolescents' Self-injurious Thoughts and Behaviors During and After Psychiatric Inpatient Hospitalization
Run by Franciscan Hospital For Children, INC. · NCT05796531 · Data updated 2026-11-12
This study is testing a new way to help teenagers aged 12-19 who have self-harm thoughts and behaviors feel better during and after their hospital stay using an app on iPads and smartphones.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 19 Years |
| Sex | All |
| Enrollment | 155 (estimated) |
| Sponsor | Franciscan Hospital For Children, INC. Academic / other |
| Locations | 1 site (Brighton, Massachusetts) |
| Status | Recruiting |
| Started | March 31, 2023 |
| Main results expected | August 15, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | July 12, 2024 |
| Trial ID | NCT05796531 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adolescents aged 12-19 who are admitted to the McLean-Franciscan Child and Adolescent Inpatient Program with self-injurious behavior, suicidal ideation, or a history of suicide attempts.
✕Probably not a fit
Patients who may not benefit from this study include those with severe cognitive impairments, acute intoxication, or those unable to participate effectively due to language barriers.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to evaluate a brief intervention using therapeutic evaluative conditioning to reduce suicidal thoughts and behaviors among adolescents aged 12-19 during and after their inpatient hospitalization. The intervention will be administered via iPads during the inpatient period and continued through smartphone apps for one month post-discharge. The study consists of a pilot phase and a randomized controlled trial phase, assessing treatment targets and outcomes at multiple time points. The goal is to determine the effectiveness and sustainability of the intervention in decreasing suicide risk during a critical period.
Why it matters
Potential benefit: If successful, this intervention could significantly reduce the risk of suicide and self-injury among adolescents during a high-risk period following hospitalization.
How similar studies have gone: While the approach of evaluative conditioning is innovative, similar interventions targeting suicide prevention in adolescents have shown promise, suggesting potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Be a patient on McLean-Franciscan Child and Adolescent Inpatient Program (MF-CAIP) of Franciscan Children's (FC) * Be 12-19 years-old * Own a smartphone * Have a parent/guardian that can provide permission * Child can assent * Presentation to the hospital with non-suicidal self-injury (NSSI), suicidal ideation or a suicide attempt. Exclusion Criteria: * Any factor that impairs an individual's ability to comprehend and effectively participate in the study, including * an inability to speak or write English fluently * the presence of gross cognitive impairment due to florid psychosis, intellectual disability, dementia, acute intoxication, etc., or the presence of extremely agitated or violent behavior * a potential discharge location anticipated to be a residential program in which the average length of stay is more than 14 days
Where it's running
-
Franciscan Hospital For Children, Inc.
Brighton, Massachusetts, United States Recruiting
Study contacts
- Study coordinator: Kelly Zuromski, PhD
- Email: kzuromski@franciscanchildrens.org
- Phone: 617-475-0595
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.