NCT07247409

Brief Summary

All participants of the Diabesity Register will receive structured assessment by nurses guided by the JADE portal at baseline including eye, feet, blood and urine examination with evaluation of BMI, blood pressure, HbA1c, lipid profile, renal and liver function tests, urine for albumin-creatinine ratio. All patients will return at 3-year for a repeat assessment of physical and psychological health, as well as changes over time.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
800

participants targeted

Target at P75+ for all trials

Timeline
41mo left

Started Oct 2025

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress19%
Oct 2025Dec 2029

Study Start

First participant enrolled

October 22, 2025

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

November 18, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

November 25, 2025

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2029

Last Updated

November 25, 2025

Status Verified

October 1, 2025

Enrollment Period

1.2 years

First QC Date

November 18, 2025

Last Update Submit

November 18, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • A composite of incidence

    Incidence of diabetes-related complications

    3 years

Secondary Outcomes (6)

  • Incidence of diabetic mellitus retinopathy

    3 years

  • Incidence of diabetic mellitus nephropathy

    3 years

  • Incidence of diabetic mellitus neuropathy

    3 years

  • Incidence of myocardial infarction

    3 years

  • Incidence of stroke

    3 years

  • +1 more secondary outcomes

Study Arms (1)

Diabesity

People with diabetes and obesity

Other: No Intervention: Observational Cohort

Interventions

It is an registry so no intervention will be used.

Diabesity

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

All study subjects will be recruited from the Diabetes Mellitus and Endocrine Centre (DMEC) at PWH. Since 1995, the PWH runs a comprehensive complication screening program as part of a quality improvement program in the DMEC. On a weekly basis, patients with diabetes mellitus undergo comprehensive assessments for risk factors and complications by nurses and health care assistants using standard protocols.

You may qualify if:

  • Type 2 diabetes;
  • Obesity reaching action level as defined as body mass index (BMI) 27.5 kg/m2 and/or waist circumference (WC) 80cm in women and 90cm in men;
  • Age between 18 and 50 years;
  • Able to conversate with smartphone technology and web-based program.
  • Able to read Chinese and communicate using Chinese.

You may not qualify if:

  • Type 1 diabetes;
  • Active malignant disease including those with history of malignant disease less than 5 years of disease-free duration;
  • Life expectancy less than 12 months;
  • Any medical illness or condition as judged by the investigators as ineligible to participate the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Medicine and Therapeutics, The Chinese University of Hong Kong (CUHK), Ward 3M, Diabetes and Endocrine Research Centre, 3/F Day Treatment Block and Children Wards (Old Block), Prince of Wales Hospital

Hong Kong, Hong Kong

RECRUITING

MeSH Terms

Conditions

Diabesity

Condition Hierarchy (Ancestors)

Diabetes ComplicationsDiabetes MellitusEndocrine System DiseasesObesityOverweightBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Alice Pik Shan Kong, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Years
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

November 18, 2025

First Posted

November 25, 2025

Study Start

October 22, 2025

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2029

Last Updated

November 25, 2025

Record last verified: 2025-10

Locations