Seattle Children's Hospital
Seattle, Washington, 98115, United States
Location status: Recruiting
Location contact
Adia Abler, BA
CONTACT
Cari McCarty, PhD
PRINCIPAL_INVESTIGATOR
Laura Richardson, MD MPH
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06701006
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, 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/caregiver 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, caregivers, and healthcare providers, will use the ISSP app (if assigned to that group) and view video content and complete three online surveys.
Interested in participating?
Request Info13 year–21 year
All sexes
Interventional
Not applicable
Seattle, Washington, 98115, United States
Location status: Recruiting
Adia Abler, BA
CONTACT
Cari McCarty, PhD
PRINCIPAL_INVESTIGATOR
Laura Richardson, MD MPH
PRINCIPAL_INVESTIGATOR
The current study aims to evaluate the Jaspr app relative to usual care among youth (ages 13-21 years) who indicate suicidal ideation in pediatric medical settings. The Jaspr app includes supported safety planning between the young person and the healthcare provider, as well as skills and support videos for youth and caregivers intended to increase coping and decrease distress with an opportunity to access these resources through an at home app. Adolescents, parents, and clinicians will participate in the project to assess the effectiveness of Jaspr augmenting usual care, compared to usual care alone. The study will use a pre-post design in which each setting begins with a control period and then transitions to the addition of Jaspr following healthcare provider training on use of the app. Participants and their parents/caregivers will receive study assessments at baseline, 1-month, and 2-month follow up timepoints, and healthcare providers complete a survey at baseline, and the end of each period (control and intervention). Study assessments with youth will ask about coping, suicidal ideation and severity, anxiety and depression, service utilization, functional impairment, access to lethal means, and acceptability of the app. Study assessments for parents/caregivers will ask about their self-efficacy in managing their youth's suicidality, acceptability of the videos/app, and service utilization for the youth. Healthcare providers will complete surveys assessing their self-efficacy in managing youth suicidality and feasibility of use of the app. Youth, their legal guardian, and healthcare providers each assent/consent to participate in the research procedures.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Youth Inclusion Criteria:
Youth Exclusion Criteria:
This is a digital app that includes supported safety planning resources in medical settings as well as coping skills and lived experience videos for adolescents, young adults and parents/caregivers that can be accessed while in the medical setting or at home.
Other names: Jaspr
Time frame: Baseline, 1 month, 2 month
Total Score on the 17-item Youth Suicide-Related Coping Scale
Time frame: Baseline, 1 month, 2 month
Total score on the Parent suicide prevention self-efficacy scale
Time frame: Baseline, end of control period, and end of intervention period
Total score on the Provider suicide Intervention Questionnaire
Time frame: Up to 1 month
Safety Planning Scoring Algorithm (SPISA) based on youth medical chart review
Time frame: Baseline, 1 month, 2 month
Total score on the online self-report version of the Columbia Suicide Severity Rating Scale (C-SSRS)
Time frame: Baseline, 1 month, 2 month
Total Score on Youth Self-Reported Generalized Anxiety Disorder -7 item scale
Time frame: Baseline, 1 month, 2 month
Youth and Parent Report on the Acceptability of Intervention Measure (AIM)
Time frame: Baseline, 1 month, 2 month
Total score on the youth reported EQ-5D-Y quality of life measure
Time frame: Baseline, 1 month, 2 month
Total Score on the Harkavy Asnis Suicide Scale ideation subscale (HASS-I),
Time frame: Baseline, 1 month, 2 month
Total score on the Patient Health Questionnaire 9
Time frame: 1 month
BRFSS Module 17 - Youth report of access to a firearm
Time frame: Baseline, 1 month, 2 month
Healthcare Provider Report on the Feasibility of Intervention Measure (FIM)
Time frame: Baseline, 2 months
Dichotomous rating of any mental health service use following baseline using chart review or indication based on parent or youth report on the Services Assessment for Children and Adolescents (SACA)
Contact information is provided by the study sponsor or research team.
University of Washington
Other
Integrated Screening and Safety Planning (ISSP) for Adolescents With Suicidal Thoughts
Acronym: ISSP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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