No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
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At a Glance
Age
18 – 44
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
9,000 (estimated)
Sponsor
Juliana CN Chan · Other
Who this trial is looking for
This trial is looking for adults aged 18 to 44 who have at least one risk factor for diabetes. Participants will take tests, answer questions, and receive personalized health reports, along with support to help reduce their risk of diabetes.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 18 and 44 years old
I have at least one risk factor for diabetes
You may not be able to join if
I have a known history of diabetes
I have conditions not suitable for the program as determined by the project team
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
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This is a community-based implementation program consisting of multiple components delivered by a multidisciplinary team to detect and prevent young onset diabetes with precision and value using biogenetic markers, digital tools, integrated care through public private partnership. Adults aged between 18 and 44 (inclusive) without known diabetes and with at least one risk factor for diabetes will u…
This is a community-based implementation program consisting of multiple components delivered by a multidisciplinary team to detect and prevent young onset diabetes with precision and value using biogenetic markers, digital tools, integrated care through public private partnership. Adults aged between 18 and 44 (inclusive) without known diabetes and with at least one risk factor for diabetes will undergo a saliva DNA and capillary blood test and complete a questionnaire. Depending on their risk levels, participants will be stratified to high risk and low risk progressors to diabetes. The high risk progressors will undergo annual oral glucose tolerance test to detect diabetes and impaired glucose tolerance (IGT). All participants will receive a personalized report indicating their genetic and modifiable risk explained by nurses or doctors. All participants will be offered regular access to webinars for education and empowerment for 2 years. The high risk group will additionally receive a 2-year risk-stratified intervention with different combinations of care interventions. These include clinical and laboratory assessment for comprehensive evaluation of cardiovascular-kidney-metabolic risks, medical and nurse consultations, empowerment by health messages, webinars, face-to-face workshops, subsidies for medications and self-monitoring tools (e.g. CGM devices, weighing scale) to motivate behavioural change. The outcomes will be analysed within the REAIM framework (reach, effectiveness, adoption, implementation and maintenance), progresssion to prediabetes or diabetes, patient reported outcomes and cost effectiveness.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Aged between 18 and 44 years old
* With at least one risk factor for diabetes
Exclusion Criteria:
* Known history of Diabetes
* With conditions considered not suitable by the project team (including illiteracy)
The risk factors for diabetes include central or general obesit…
Inclusion Criteria:
* Aged between 18 and 44 years old
* With at least one risk factor for diabetes
Exclusion Criteria:
* Known history of Diabetes
* With conditions considered not suitable by the project team (including illiteracy)
The risk factors for diabetes include central or general obesity, family history of diabetes, smoking history, history of hypertension/ high blood glucose level/ abnormal lipid level/ vascular disease/ fatty liver, history of gestational diabetes/ polycystic ovary syndrome/ delivery of baby≥ 4kg (for women only), and less than 150mins of physical activity every week.
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