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Chinese Alliance for Type 1 Diabetes Multi-center Collaborative Research

Recruiting
Conditions
Type 1 Diabetes Mellitus
Registration Number
NCT04096794
Lead Sponsor
Second Xiangya Hospital of Central South University
Brief Summary

The China Alliance for Type 1 Diabetes (CAT1D) is committed to exploring and implementing the model of graded diagnosis and treatment of type 1 diabetes and comprehensive management of outpatient service, carrying out a series of educational activities for patients, and cooperating in the development of multi-center prospective clinical research on type 1 diabetes.

Detailed Description

1. Through the CAT1D, expand the cohort construction of type 1 diabetes patients and first-level relatives in China, establish the electronic information database of type 1 diabetes, and lay a foundation for obtaining the research data of type 1 diabetes in China.

2. observe and study the occurrence and development rules of acute and chronic complications of type 1 diabetes in China, analyze the influencing factors, and provide intervention means for reducing acute complications and preventing chronic complications.

3. Through the established management platform and structured education system, verify and promote the comprehensive management mode based on structured education, and build a standard treatment plan and process based on evidence-based science and suitable for Chinese people and medical background.

4. By using mobile health (mHealth) and Artificial Intelligence (AI) technologies, a new mode of intelligent structured education is established, which provides a new way to explore the individualized education management mode and improve the outcome of chronic diseases through modern technology.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
500
Inclusion Criteria
  • Individuals diagnosed with Type 1 Diabetes according to the 1999 World Health Organization report
  • Written informed consent from the patient or family representative;
  • Individuals who own smartphone and are capable of using wechat or apps
Exclusion Criteria
  • Non-t1dm patients with autoimmune polyendocrine adenopathy syndrome (APS) are the first disease
  • With mental disorders
  • Have any other condition or disease that may hamper from compliance with the protocol or complication of the trial

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
changes in serum hemoglobin A1c levelBaseline and every up to 12 weeks afterwards

A1c reflects the average blood glucose level in the past 3 months.

Secondary Outcome Measures
NameTimeMethod
Stool samplesBaseline and every up to 12 weeks afterwards
Adverse effectsBaseline and every up to 12 weeks afterwards

Adverse effects are recorded at each time-point of the follow-up

Systolic blood pressureBaseline and every up to 12 weeks afterwards

Systolic blood pressure

Height in metersBaseline and every up to 12 weeks afterwards

Height in meters will be measured

C-peptideBaseline and every up to 12 weeks afterwards

C-peptide are measured before and 2-hour after a mixed meal tolerance test at each follow-up of this study

changes in Time in range (TIR)Baseline and every up to 12 weeks afterwards

TIR measures the time where the blood glucose remains within the proposed target range.

Diastolic blood pressureBaseline and every up to 12 weeks afterwards

Diastolic blood pressure

Change in lipid profilesBaseline and every up to 12 weeks afterwards

Including triglyceride, total cholesterol, HDL-cholesterol and LDL-cholesterol

Weight in kilogramsBaseline and every every up to 12 weeks afterwards

Weight in kilograms will be measured

Fasting blood glucoseBaseline and every up to 12 weeks afterwards

the blood sugar level after fasting for eight hours

Change in titer of autoantibodiesBaseline and every up to 12 weeks afterwards

Trial Locations

Locations (1)

Institute of Metabolism and Endocrinology, Second Xiangya Hospital, Central South University

🇨🇳

Changsha, Hunan, China

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