Actively Recruiting
PATSy Perspectives on Antibiotics and Tracking Symptoms in Children - a Mixed Methods Feasibility Study
Led by Murdoch Childrens Research Institute · Updated on 2025-09-22
300
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
Sponsors
M
Murdoch Childrens Research Institute
Lead Sponsor
R
Royal Children's Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating families' perspectives and decision-making about how long children aged 4 to 17 should take oral antibiotics for uncomplicated bacterial infections. This study focuses on children treated at the Royal Children's Hospital Emergency Department, either discharged with oral antibiotics or transferred to Hospital-in-the-Home for IV antibiotics before switching to oral therapy. The study also assesses how practical and acceptable it is to use a Garmin Smartwatch and the WeGuide platform to track children's symptoms during treatment. The study involves all eligible participants completing daily symptom questionnaires throughout their antibiotic course, a one-time survey about views on antibiotic duration, and two short follow-up questionnaires on days 14 and 28 to record if antibiotics were restarted and to gather feedback on study procedures. A small group of about 60 participants will wear a Garmin Smartwatch during their antibiotic treatment to collect data on heart rate, skin temperature, sleep, and activity, which will be compared with parent-reported symptoms. Participants and their parents will be involved in completing surveys and, if selected, wearing the smartwatch while antibiotics are taken. Data collection occurs through the WeGuide platform, which manages enrollment, consent, and survey responses. Researchers will measure how often the smartwatch is worn, any issues reported with the device or questionnaires, and the agreement between smartwatch data and parent reports. The study will also track antibiotic use and symptom resolution up to 28 days after starting antibiotics. The total participation duration varies based on antibiotic course length and follow-up timing.
CONDITIONS
Brief Title
Perspectives on Antibiotics and Tracking Symptoms in Children
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between the ages of 63 4 years and 63 17 years at enrolment
- Diagnosed with urinary tract infection, cellulitis, impetigo, pharyngitis, tonsillitis, respiratory tract infections, or otitis media at RCH Emergency Department
- Prescribed oral antibiotics either immediately or after switching from IV antibiotics following transfer to Hospital-in-the-Home
- Parent or guardian provides signed and dated informed consent form
You will not qualify if you...
- Parent or guardian does not speak English
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote) for eligibility assessment and consent
Duration - Duration of antibiotic course (up to 10 days)
Participants take prescribed oral antibiotics as standard care while completing daily symptom tracking questionnaires and, for some, wearing a Garmin Smartwatch to collect health data.
Daily symptom tracking questionnaires and daily Garmin Smartwatch use for those assigned
Duration - Up to 28 days after starting antibiotics
Participants complete follow-up questionnaires on day 14 and day 28 to report on antibiotic use, health status, and provide feedback on study procedures and devices.
2 follow-up questionnaires at day 14 and day 28
Trial Site Locations
Total: 1 location
1
Royal Children's Hospital
Melbourne, Victoria, Australia, 3052
Actively Recruiting
Research Team
A
A/Prof Penelope Bryant
L
Lucy Hill
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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