Oral glucose tolerance test and HbA1c
Diagnostic TestFollowing overnight fasting for 8 hours
NCT Number: NCT07452159
This observational study aims to develop novel contemporary risk factor tools for detecting young onset diabetes (under 40y) in young Asians in Singapore. The investigators aim to recruit 3000 people not currently known to have diabetes, selected across age and Body Mass Index categories, and perform formal diagnostic tests for diabetes (oral glucose tolerance test and HbA1c). The participants will also undergo continuous glucose monitoring sensor, keep a food diary, and undergo body composition analysis using bioimpedance analysis, handgrip measurements for muscle strength, and sociobehavioural profiling through download of a curated list of social media interactions. The participants will also have a blood sample retrieved and stored for subsequent comparison between people with normal glucose versus abnormal glucose levels. The whole group will also have another blood sample stored for whole gene analysis.
Trial opening soon.
Get Notified21 year–39 year
All sexes
Observational
Overarching aim: To improve the case detection rate of T2D in young Singaporeans adults aged 21-40y.
Specific Aim 1: To conduct a case-finding study for T2D and prediabetes through age- and BMI-stratified sampling in a contemporary population of young Singaporean adults aged 21-40y.
Specific Aim 2: To identify novel risk factors and develop a composite score to improve the detection rate for Asian YOD and prediabetes. These include non-traditional predictors such as glucometrics from continuous glucose monitoring (CGM), body composition measures, and socio-behavioural analyses.
Specific Aim 3: To identify the contribution of genomic differences to the risk of Asian Young Onset Diabetes
To fulfil Aim 1 within the first 1 to 2 years, the investigators plan to perform island-wide screening for diabetes or prediabetes amongst people aged 21-40y (n=3000). Recruitment will be stratified firstly by age categories (21-25y, 25-30y, 30-35y, 35-40y), aiming for n=750 per age category, followed by BMI categories of normal, overweight or obese by Asian thresholds (<23kgm2, 23-27.5kg/m2 and >=27.5kg/m2) within each age group. Participants will be recruited through online and print media including social media advertisements, word of mouth and /or referrals. A study poster advert will be posted online and in print, which will then direct participants to a webpage www.thdiary.sg which will explain the study design further and eligibility requirements and additional study details. The partiipants can proceed to register themselves via FORMSG on this webpage and if they meet the criteria they will be directed to CALSG to book an appointment with the study team.
Upon consent and recruitment, the following will be done:
In Aim 2, the investigators aim to identify novel contemporary risk markers associated with T2D or prediabetes in young adults. This aim will not require another study visit from participants. Stored samples from Aim 1 baseline OGTT venipuncture will be used as well as the data retrieved from the study procedures in aim 1. Those who are diagnosed with T2D and prediabetes (estimated n=200 each), together with a normoglycaemic group (n=200) from Aim 1 will have the following done to enable diabetes subtyping: lipids, C-peptide, Insulin levels, Glutamic Acid Decarboxylase (GAD), Islet Antigen 2 (IA-2) Antibodies (Ab) and Zinc Transport 8 (ZnT8) Ab.
A composite score will then be developed for the diagnosis of prediabetes and diabetes. The dataset will be split into development and validation sets. Logistic regression modelling and Receiver Operating Characteristics (ROC) curve analysis will be employed to develop a composite score in identifying people with T2D or prediabetes, based on the sample with 200 newly diagnosed T2D, 200 prediabetes and 200 normoglycaemic participants. With the development set, two models will be fitted to predict a subject belongs to T2D, prediabetes or normoglycaemia: (a) candidate predictor variables of all abovementioned indicators and their derivatives, including sociodemographic, family history of diabetes and comorbid conditions, dietary intake, physical activity levels, body composition metrics, health-seeking behaviours, as well as CGM biomarkers, and (b) candidate predictor variables of all these variables except those extracted / derived from CGM. Variable selection methods will be employed to determine final models with optimal predictability, parsimony and model fit indices. Two composite scores, including and not including CGM biomarkers, will then be defined by the final selected models.
To fulfil aim 3, stored blood from participants will be used in ongoing large scale genomic studies such as the National Precision Medicine's Phase 3 programme. In this program, participants will have whole genome sequencing performed under research, with a cluster specific centralized genomics team made up of clinical geneticists, bioinformaticians, variant curators, and genetic counsellors available to process the genetic specimens end to end (genomics innovation hub). This would involve curating genes relevant to the disease subtype, in this case, diabetes, but also returning incidental findings that are Tier 1 American College of Medical Genetics and Genomics (ACMG) conditions. VCF files from the participants of this study will be returned to this study team so that further research can be done to determine if genomic information can further help risk stratify Asian YOD.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Following overnight fasting for 8 hours
Body Mass Index, Waist-Hip ratio, Blood pressure
Body composition analysis
Handgrip strength measured using Jamar Dynanometer
Use of Retrospective continuous glucose monitoring sensor (Freestyle Libre Pro IQ)
Including written food records and photographs for all food and drink intake
Retrieval of sociodemographic details, family history of diabetes and comorbid conditions, information on dietary intake, physical activity levels, and health seeking behaviour. This includes average daily step count for 7/30 days.
Form to feedback on any sensor skin reactions
This will involve a highly curated list of information to be retrieved from Facebook, Instagram and TikTok to enable AI-led sociobehavioural profiling. This will not retrieve any information on posts, photos, likes, comments, reactions or any item that will express intent.
Whole blood sample will be retrieved and stored before being sent for whole genome sequencing at a later stage.
Time frame: Baseline
Fasting glucose >/=7mmol/l or 2-hour glucose >/=11.1 mmol/l on oral glucose tolerance test or HbA1c >/=7%.
Time frame: Baseline
Fasting glucose >/=5.7mmol/l or 2-hour glucose >/=7,8 mmol/l on oral glucose tolerance test or HbA1c >/= 5.7%.
Contact information is provided by the study sponsor or research team.
Daphne SL Gardner, BA, BMBCh (Oxon), MRCP (UK)
CONTACT
Navreen Kaur
CONTACT
Singapore General Hospital
Other
Acronym: DIARY
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.