Status:
NOT_YET_RECRUITING
Non-Expert Acquisition & Remote Expert Review of Screening Echocardiography Images From Child Health & AnteNatal Clinics
Lead Sponsor:
Menzies School of Health Research
Collaborating Sponsors:
The University of Western Australia
Telethon Kids Institute
Conditions:
Rheumatic Heart Disease
Eligibility:
All Genders
5+ years
Phase:
NA
Brief Summary
The Non-Expert Acquisition and Remote Expert Review of Screening echocardiography images from Child health and AnteNatal clinics (NEARER SCAN) study is a co-designed, implementation research project t...
Detailed Description
This study titled 'Non-Expert Acquisition and Remote Expert Review of Screening echocardiography images from Child health and AnteNatal clinics' (NEARER SCAN; "LENO BESIK" in Tetum) aims to co-design,...
Eligibility Criteria
Inclusion
- Inclusion Criteria in Australia:
- Any child between the age of 5 - 20 years old living in the participating community
- Pregnant women at high risk for RHD undergoing antenatal appointments or a hospital admission will be invited to participate. High risk for RHD will be defined as being from an area where RHD all-age prevalence is \>1/1000 RHD or acute rheumatic fever incidence \>30/100,000 per year in 5-14-year-olds. For practical purposes, this means Aboriginal women living in urban, rural or remote communities in northern Australia, or immigrants from high-risk settings.
- Inclusion criteria for Timor-Leste:
- Any child between the age of 5-20 years old and any pregnant woman.
- Exclusion criteria for Australia and Timor-Leste:
- Women who are unable to consent due to physical, mental, or intellectual disability will be excluded. Women and children with known existing cardiac disease will NOT be excluded since evaluation of severity and change in severity during pregnancy will be tracked, and data will inform the calculation of prevalence.
Exclusion
Key Trial Info
Start Date :
April 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2025
Estimated Enrollment :
1500 Patients enrolled
Trial Details
Trial ID
NCT06002243
Start Date
April 1 2024
End Date
December 1 2025
Last Update
March 18 2024
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