Diabetes In Asians at Risk in Youth (DIARY)

March 1, 2026 updated by: Singapore General Hospital

Diabetes in Asians at Risk in Youth

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.

Study Overview

Detailed Description

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:

  1. Anthropometric measurements alongside traditional risk factors including blood pressure (BP), and waist-hip-ratio.
  2. Body Impedance Analysis. This is a painless way to measure what the body is made of and involves standing on a special scale and holding onto handles.
  3. Venipuncture will be conducted for an oral glucose tolerance test (OGTT) for 0 min, 1h and 2h glucose readings and HbA1c and storage.
  4. Download of selected social media data (not directly containing personal data or posts) for up to 1 year preceding the visit from facebook, instagram and tiktok.
  5. Continuous glucose monitor (CGM) sensor insertion. On the day of CGM insertion, a pre-insertion questionnaire (using form.sg, DIARY skin reaction form 1 before sensor wear) will be filled in which includes a picture of the site before sensor insertion.
  6. A survey will also be conducted to ascertain sociodemographic (employment, type of residence) and educational status, family history of diabetes and comorbid conditions (if any), the individual's dietary intake, physical activity levels, and health-seeking behaviour. This survey will also include a section to fill in their average daily step count for 7/30 days. The participant will be guided to look for their step count data over 7 or 30 days (depending on what is available) from their smartphone activity tracker (this includes Apple Health, Samsung Health or Google Fit or any other activity tracker). This information will then be entered into the survey form on form.sg. No screenshots or data export is required.
  7. Handgrip measurements
  8. Second and third venipunctures for second part of OGTT.
  9. Collection of dietary data via a digital food log

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.

Study Type

Observational

Enrollment (Estimated)

3000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Islandwide across Singapore

Description

Inclusion Criteria:

  • Asian/Part Asian ethnicity living in Singapore, not known to have diabetes

Exclusion Criteria:

  • Pregnancy women
  • Non-Asian ethnicity
  • On active cancer/steroid therapy
  • Haemoglobinopathies or haemolytic anaemia
  • Previous bariatric surgery
  • Previous partial/total pancreatectomy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Singaporeans of Asian ethnicity under 40 years
Not previously known to have diabetes
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diagnosis of diabetes
Time Frame: Baseline
Fasting glucose >/=7mmol/l or 2-hour glucose >/=11.1 mmol/l on oral glucose tolerance test or HbA1c >/=7%.
Baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diagnosis of pre-diabetes
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%.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

March 18, 2026

Primary Completion (Estimated)

January 2, 2029

Study Completion (Estimated)

January 2, 2029

Study Registration Dates

First Submitted

December 1, 2025

First Submitted That Met QC Criteria

March 1, 2026

First Posted (Actual)

March 5, 2026

Study Record Updates

Last Update Posted (Actual)

March 5, 2026

Last Update Submitted That Met QC Criteria

March 1, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

This is an observational study, only aggregated data will be provided. In addition, there is a part of the study that retrieves information social media activity. There is a potential that individual level data can lead to sensitive personal information being revealed.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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