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Recruiting NCT07136584

NCT07136584 SOS for Caregiver Wellbeing

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Clinical Trial Summary
NCT ID NCT07136584
Status Recruiting
Phase
Sponsor Murdoch Childrens Research Institute
Condition Mental Health
Study Type INTERVENTIONAL
Enrollment 100 participants
Start Date 2025-10-22
Primary Completion 2026-08

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Screening, Outcomes and Referral Pathways

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 100 participants in total. It began in 2025-10-22 with a primary completion date of 2026-08.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Parents and caregivers of children who have a chronic condition carry a large care burden and are at higher risk of having mental health symptoms. This study aims to see if completion of a mental health questionnaire by parents / caregivers at or before the child's paediatric appointment can help identify any symptoms of stress, anxiety or depression. Following the questionnaire, parents / caregivers will be provided with the results of the questionnaire along with an information resource sheet. This will include information on anxiety, stress and depression, as well as different agencies they can contact to get support. Parents / caregivers will be followed up at 3 and 6 months to see if they have any changes to mental health and quality of life, and whether they accessed any support services. Participants who did not complete the 3-month survey will be asked at the 6-month clinic visit to provide responses on an iPad to up to 5 questions selected from the 3-month survey. A text message will be sent prior to the visit to inform them. The primary aim for this trial is to see whether parents / caregivers find this process acceptable, and whether it can work in a busy hospital clinic.

Eligibility Criteria

Inclusion Criteria: * must be a parent of a child \<18yo in an outpatient clinic at Royal Children's Hospital (in enrolled clinics either neuromuscular or diabetes) * able to complete a consent form in English without an interpreter Exclusion Criteria: * need for an interpreter to complete informed consent

Contact & Investigator

Central Contact

Nadia Coscini, BA, MBBS, MSc

✉ nadia.coscini@mcri.edu.au

📞 +61 3 8341 6762

Principal Investigator

Nadia Coscini, BA, MBBS, MSc

PRINCIPAL INVESTIGATOR

Murdoch Children's Research Institute & University of Melbourne

Frequently Asked Questions

Who can join the NCT07136584 clinical trial?

This trial is open to participants of all sexes, studying Mental Health. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07136584 currently recruiting?

Yes, NCT07136584 is actively recruiting participants. Contact the research team at nadia.coscini@mcri.edu.au for enrollment information.

Where is the NCT07136584 trial being conducted?

This trial is being conducted at Parkville, Australia.

Who is sponsoring the NCT07136584 clinical trial?

NCT07136584 is sponsored by Murdoch Childrens Research Institute. The principal investigator is Nadia Coscini, BA, MBBS, MSc at Murdoch Children's Research Institute & University of Melbourne. The trial plans to enroll 100 participants.

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