RECRUITING

Integrated Suicide Supports and Safety Planning for Youth

Conditions

Suicidal Ideation Suicidal Behavior adolescents young adults suicide prevention health services research

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to evaluate an app to help keep teens and young adults with suicidal thoughts safe. The app includes a safety plan created by adolescents and healthcare providers in the clinic, and videos to encourage supportive communication and skills for teens and young adults to stay safe. The main question it aims to answer is whether the use of an app can increase youth suicide-related coping for youth with suicidal ideation, parent suicide prevention self-efficacy, and healthcare provider self-efficacy in suicide management. Researchers will compare usual care to usual care with the app. Participants, including adolescents, their caregivers and healthcare providers, will use the ISSP app (if assigned to that group) and complete three online surveys.

Official Title

Integrated Screening and Safety Planning (ISSP) for Adolescents With Suicidal Thoughts

Quick Facts

Study Start:2025-06-27

Study Completion:2026-04-30

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06701006

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:13 Years to 21 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:CHILD, ADULT

Inclusion Criteria	Exclusion Criteria
* Age 13 -21 years, an Ask Suicide Questions (ASQ) screen score of 1-4 with no current plan or intent (item 5 negative and as assessed by their clinical providers) and/or a risk level of suicidal thoughts and behaviors (STB) that constitutes the need for higher level assessment (such as the BSSA or C-SSRS) and/or a safety plan, as determined by an HCP because of a risk screener or a clinical interaction * Parents/guardians: One "parent" per AYA will also be invited to participate. * HCPs: All HCPs in participating clinics who may conduct assessments of SI (physicians, nurse practitioners/physician's assistants, social workers, nurses, psychologists) will be invited to participate. * All subjects must have access to the internet and a computer or tablet device.	* Previously recruited to other affiliated Suicide Care Research Center study, no phone access, no parent willing to participate, non-English speaking, or already has a suicide safety plan that is being overseen by a mental health specialist.

Inclusion Criteria

Exclusion Criteria

* Age 13 -21 years, an Ask Suicide Questions (ASQ) screen score of 1-4 with no current plan or intent (item 5 negative and as assessed by their clinical providers) and/or a risk level of suicidal thoughts and behaviors (STB) that constitutes the need for higher level assessment (such as the BSSA or C-SSRS) and/or a safety plan, as determined by an HCP because of a risk screener or a clinical interaction
* Parents/guardians: One "parent" per AYA will also be invited to participate.
* HCPs: All HCPs in participating clinics who may conduct assessments of SI (physicians, nurse practitioners/physician's assistants, social workers, nurses, psychologists) will be invited to participate.
* All subjects must have access to the internet and a computer or tablet device.

* Previously recruited to other affiliated Suicide Care Research Center study, no phone access, no parent willing to participate, non-English speaking, or already has a suicide safety plan that is being overseen by a mental health specialist.

Contacts and Locations

Study Contact

Laura Richardson, MD, MPH

CONTACT

206-987-2028

lpr@uw.edu

Principal Investigator

Laura Richardson, MD, MPH

PRINCIPAL_INVESTIGATOR

University of Washington

Study Locations (Sites)

Seattle Children's Hospital

Seattle, Washington, 98115

United States

Collaborators and Investigators

Sponsor: University of Washington

Laura Richardson, MD, MPH, PRINCIPAL_INVESTIGATOR, University of Washington

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-06-27

Study Completion Date2026-04-30

Study Record Updates

Study Start Date2025-06-27

Study Completion Date2026-04-30

Terms related to this study

Keywords Provided by Researchers

adolescents
young adults
suicide prevention
health services research

Additional Relevant MeSH Terms

Suicidal Ideation
Suicidal Behavior