By InvitationNot Applicable

SAFETY-Parent: Online Learning Module to Support Parents of Suicidal Youth

United States65 participantsStarted 2024-06-10

Plain-language summary

This project aims to adapt the parent component of Safe Alternatives for Teens and Youth (SAFETY) outpatient intervention to SAFETY-Parent (SAFETY-P), a self-paced interactive learning module for parents, to be implemented as an augmentation for youth being seen for suicidal ideation, suicidal behavior, or recent suicide attempts across multiple settings at Nationwide Children's Hospital (NCH, Columbus, Ohio).

Who can participate

Age range10 Years – 18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Youth is currently in treatment with the Critical Assessment and Treatment Clinic (CATC) at NCH for suicidal thoughts or behaviors
✓. Youth is between the ages of 10-18 (18-year-old youth must still be in high school and living at home with parents for duration of the study)
✓. At least one parent is able to participate
✓. Youth and parent are fluent in English

Exclusion criteria

✕. The youth or parent has an acute psychiatric or medical condition that would interfere with their ability to participate in study procedures
✕. Lack of access to a digital device (smartphone, iPad, tablet computer, desktop, laptop PC)

What they're measuring

Satisfaction with intervention on the Peabody Treatment Progress Battery (PTPB) - Service Satisfaction Scale (SSS)

Timeframe: 1 month, 3 months

Use of intervention as measured by information provided by the Brainer Learning Management System (LMS)

Timeframe: 1 month, 3 months

Intervention feasibility and acceptability on the SAFETY-P Satisfaction Scale

Timeframe: 1 month, 3 months

Intervention usability on the System Usability Scale

Timeframe: 1 month

Intervention acceptability on the Mobile Application Rating Scale: User Version (uMARS)

Timeframe: 1 Month

Utilization of mental health services on the Child and Adolescent Services Assessment: Brief and Adapted version (CASA)

Timeframe: Baseline, 1 month, 3 months

Trial details

NCT IDNCT06460220

SponsorJennifer Hughes

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-12

View on ClinicalTrials.gov More Suicide trials

Plain-language summary

Who can participate

Age range10 Years – 18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Youth is currently in treatment with the Critical Assessment and Treatment Clinic (CATC) at NCH for suicidal thoughts or behaviors
✓. Youth is between the ages of 10-18 (18-year-old youth must still be in high school and living at home with parents for duration of the study)
✓. At least one parent is able to participate
✓. Youth and parent are fluent in English

Exclusion criteria

✕. The youth or parent has an acute psychiatric or medical condition that would interfere with their ability to participate in study procedures
✕. Lack of access to a digital device (smartphone, iPad, tablet computer, desktop, laptop PC)

What they're measuring

Satisfaction with intervention on the Peabody Treatment Progress Battery (PTPB) - Service Satisfaction Scale (SSS)

Timeframe: 1 month, 3 months

Use of intervention as measured by information provided by the Brainer Learning Management System (LMS)

Timeframe: 1 month, 3 months

Intervention feasibility and acceptability on the SAFETY-P Satisfaction Scale

Timeframe: 1 month, 3 months

Intervention usability on the System Usability Scale

Timeframe: 1 month

Intervention acceptability on the Mobile Application Rating Scale: User Version (uMARS)

Timeframe: 1 Month

Utilization of mental health services on the Child and Adolescent Services Assessment: Brief and Adapted version (CASA)

Timeframe: Baseline, 1 month, 3 months