RecruitingACTRN12625001287426

Feasibility and acceptability of EDBridge: A brief contact intervention for adolescents at risk of suicide and their parents

Feasibility and acceptability of EDBridge: A multi-component brief contact intervention program involving safety planning, psycho-educative resources, and automated follow-up text message support for adolescents at risk of suicide and their parents/caregivers, investigating the impact on suicide risk, suicide-related coping, parent mental health and self-efficacy in managing adolescent suicide risk, and community treatment engagement.


Sponsor

Deakin University

Enrollment

144 participants

Start Date

Nov 5, 2025

Study Type

Interventional

Conditions

Summary

Suicide remains a leading cause of death for Australian adolescents, and suicide and self-harm related Emergency Department presentations are rising. Brief contact interventions are an important component of comprehensive treatment approaches for adolescent suicide risk. Research has found that families feel excluded from their adolescent’s care in the ED and don’t receive sufficient information about how to support them, despite evidence suggesting involving families in adolescent suicide prevention interventions leads to better outcomes. Additionally, there is a need to provide continuity of care after discharge from the ED. The EDBridge Pilot Feasibility & Acceptability trial involves a multi-component brief-contact intervention for adolescents aged 12-18 who are discharged from an Emergency Department with suicidal thoughts or behaviours, and their parents/carers. It involves a suicide safety planning intervention for adolescents, a parent factsheet resource to support parents to manage adolescent suicide risk outside the ED, and an automated follow-up text message support program for both adolescents and their parents/carers. The aims of this trial are to determine whether EDBridge is feasible (that is, how easy or practical EDBridge is to provide), and acceptable to adolescents, parents, and clinicians. We also aim to collect early information about whether EDBridge can help improve the mental health and suicide-related symptoms of parents and adolescents, and increase their engagement with community mental health support. We hypothesise that EDBridge will be feasible and acceptable to clinicians, adolescents, and parents. We also hypothesise that the pilot trial will give early indication that EDBridge can support adolescents and parents to improve suicide-related and mental health outcomes and increase engagement with community mental health support.


Eligibility

Sex: Both males and femalesMin Age: 12 Yearss

Plain Language Summary

Simplified for easier understanding

When a young person is seen in an emergency department after a suicidal crisis, the period after they are discharged home is a critical and often under-supported time. Families often feel excluded from their child's care and unsure how to help. EDBridge is a new multi-part programme designed to bridge this gap — it includes a safety planning conversation with the adolescent, a factsheet resource for parents and carers, and an automated follow-up text message programme for both the young person and their family in the weeks after discharge. This pilot trial is testing whether EDBridge is practical to deliver and acceptable to adolescents, parents, and the clinicians who work in the emergency department. Early signals of whether it improves mental health and helps young people engage with ongoing community support will also be examined. You may be eligible if you are an adolescent aged 12 to 18 who has presented to the participating paediatric emergency department with suicidal thoughts or behaviour and is being discharged home, accompanied by a parent or carer. Families need a mobile phone and the ability to read English to receive the text message component. Young people in out-of-home care or without a parent present at the time of presentation are not eligible for this pilot.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

EDBridge involves three intervention components including safety planning (for teen participants), a psychoeducative factsheet (for parent participants), and an automated text message support program

EDBridge involves three intervention components including safety planning (for teen participants), a psychoeducative factsheet (for parent participants), and an automated text message support program (for teen and parent participants). All teens who enrol in this study will be given access to the safety planning and text message intervention components. All parents who enrol in this study will be given access to the psychoeducative factsheet and text message intervention components. All intervention components will be delivered in the participating ED for seven months. 1. Safety planning (for adolescents) Adolescent participants will develop a collaborative safety plan with a trained paediatric emergency psychiatry clinician during their routine assessment in the Paediatric Emergency Department (ED). Adolescents will first be offered to develop a safety plan using the Beyond Now smartphone app, with a paper or verbal safety plan offered as alternatives. Beyond Now is a suicide safety planning smartphone application initially developed by Beyond Blue (now owned by Lifeline) that is freely available to the public on all major app stores. It has not been specifically designed for this study. The Beyond Now safety planning app contains seven steps for managing a suicidal crisis, including 1. identifying warning signs of a suicidal crisis, 2. making the environment safe (e.g., removing access to lethal means), 3. reasons for living, 4. internal coping strategies, 5. social contacts and places for distraction, 6. social support for help with a suicidal crisis, and 7. professional supports. The paper based safety plan will follow the same format as Beyond Now. If adolescents already have a safety plan developed, they will have the option to transition the plan to Beyond Now or an alternative. After developing a safety plan (with or without Beyond Now), adolescent participants will engage with their safety plan at their own discretion and will not be asked to use the app or their safety plan for any minimum duration once discharged from the ED (however some text messages as part of the text message intervention will encourage engagement with their safety plan). Clinicians will receive training on developing safety plans using Beyond Now two weeks prior to the anticipated first enrolment. Clinicians will record whether a participant safety plan was developed with Beyond Now, paper-based format, or verbally. Adherence to app usage will not be directly monitored (e.g., via app analytics). Adolescent participants will be surveyed on their engagement with their safety plan during follow up surveys at Week 2 and Week 12 post enrolment. Because participants are only eligible for the study if they are discharged out of the hospital system, and there is no follow up appointments with the ED clinician (due to the nature of cross-sectional ED assessments), participants will not have their safety plan reviewed by ED clinicians unless they return to the ED or discuss their safety plan with a community-based clinician (e.g., private psychologist). Reviewing of safety plans is not within the scope of the current research protocol. 2. Parent/caregiver psychoeducative factsheet (for parents/carers) Parents/caregivers of adolescents presenting to the ED will receive a paper-based psycho-educative factsheet resource from the trained paediatric emergency psychiatry clinician (or a researcher) upon discharge from the ED. The two-sided A4 factsheet includes strategies for managing adolescent suicide risk in the 24-48 hours post-discharge, options for seeking treatment and caregiver support, and psycho-education. The factsheet is tailored to the recruitment site and was co-designed by researchers, young people with lived experience and their parents, and clinicians. 3. Text message support (for adolescents and parents) Both adolescents and parents will receive a one-way, automated follow-up text message support program post-discharge from the ED. The trained paediatric emergency psychiatry clinician will activate the text message program using a web platform developed for the trial. Participants will be randomly allocated to one of two text-message intervention arms: a short-term (2-week) or long-term (3-month) arm. Parents in the short-term arm will receive 14 messages and adolescents in the short-term arm will receive 12 messages. For adolescents, text messages contain information and strategies about managing a suicidal crisis, safety planning, transitioning back to school/work, problem solving, places to get support (e.g., online support, crisis support, longer term mental health treatment), and psychoeducation about suicide and suicide risk factors (e.g., self-harm). Parents will receive information and strategies about safety planning for their teen, how to monitor for and respond to changes in suicide risk, connecting with their teen, places their teen can get mental health support (including crisis support), and options for parent/caregiver support. The long-term intervention arm does not contain additional or new information for parents or adolescents but rather involves reminders about previously delivering strategies and information. Text message delivery will be monitored via Twilio, a cloud-based communication service that is being used to deliver text messages.


Locations(1)

Monash Children’s Hospital - Clayton

VIC, Australia

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ACTRN12625001287426