Plan and Protect: Safety Planning for Teens in Rural Emergency Departments (NCT07325474)
Development & Implementation of Culturally Sensitive Safety Planning to Reduce Suicide Risk in Adolescents Seeking Care in Rural Emergency Departments
๐ฉบ Plain-English Summary (8th-Grade Level)
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 with suicidality. 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
Who can join: Review the eligibility criteria below.
Location: Cheshire Medical Center โ Keene, New Hampshire
Age range: 12 Years to 17 Years
๐งช Interventions in This Study
- Plan & Protect safety planning intervention (BEHAVIORAL)
- Care as usual (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (4 Sites)
- Cheshire Medical Center โ Keene, New Hampshire
- Dartmouth-Hitchcock Medical Center โ Lebanon, New Hampshire
- Alice Peck Day Memorial Hospital โ Lebanon, New Hampshire
- New London Hospital โ New London, New Hampshire
๐ Contact the Study Coordinator
Phone: (603) 646-5614
Email: jacqueline.a.pogue@dartmouth.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Suicide Ideation
- A New Clinical Model for the Engagement of Latinx Youth With Suicidal Behavior โ Providence, Rhode Island
Explore by condition: All Suicide Ideation clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.