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Plan and Protect: Safety Planning for Teens in Rural Emergency Departments

Recruiting

Development & Implementation of Culturally Sensitive Safety Planning to Reduce Suicide Risk in Adolescents Seeking Care in Rural Emergency Departments

Who can join

Ages 12 and older · All sexes

Full eligibility criteria
Inclusion criteria for children:

* 12-17 years of age (and their parent/caregiver(s))
* Ability to speak and complete surveys in English
* History of emergency department visit for suicidality, self-harm or mental health crisis
* Medically stable

Exclusion criteria for children:

* Cognitive or developmental delays that preclude program participation based on clinical team assessment
* Diagnosis of psychosis
* Primary diagnosis of an eating disorder
* Parent/guardian not able to provide consent in English
* Clinical team concern for patient or staff safety based upon active behavioral concerns
* Parent/guardian not available to provide consent (e.g youth is in child protective custody/ward of the state)

Inclusion criteria for parents/caregivers:

* Parent or caregiver of an eligible child
* 18 years old or older
* Ability to speak and complete surveys in English

Exclusion criteria for parents/caregivers:

-Inability to understand key aspects of the study

About the study

The goal of this observational study is to determine whether implementing a culturally sensitive, tablet-based safety planning program called Plan \& Protect (P\&P) within rural emergency departments can improve home safety and reduce suicide risk in adolescents presenting to the emergency department with suicide-related concerns.

The main questions it aims to answer are:

* Will implementing P\&P increase caregiver-reported home safety (reduce access to firearms and unsafe medication storage) for adolescents 12-17 years old presenting to rural EDs with suicidal ideation, self-harm, or mental health crisis? * Will implementing P\&P decrease adolescent-reported perceived suicide risk and related outcomes (e.g., suicide events, and attendance at follow-up mental healthcare)?

Researchers will compare outcomes for adolescents and caregivers receiving P\&P (implemented as the new standard of care at sites during the intervention periods) to those receiving usual care (prior to P\&P implementation at those hospitals) to see if P\&P increases home safety and decreases suicide risk and related healthcare utilization.

Participants will, if clinically appropriate:

* Complete the tablet-based P\&P modules during their ED visit * Complete self-report measures at baseline, \~30 days, and \~3 months post-discharge * A subset will also participate in semi-structured interviews

What is being tested

Sponsor: Dartmouth-Hitchcock Medical Center · Participants: 550 · Started: Aug 3, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07325474

Locations in the U.S.

New HampshireValley Regional Hospital, Claremont (Not yet recruiting)
Cheshire Medical Center, Keene
Alice Peck Day Memorial Hospital, Lebanon
Dartmouth-Hitchcock Medical Center, Lebanon
New London Hospital, New London
VermontMount Ascutney Hospital, Windsor

Conditions

From ClinicalTrials.gov, data retrieved Oct 3, 2026. Each study sets its own eligibility; the study team decides who can join.