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Research on the Early Recognition, Classification and Precision Intervention System of Diabetes Based on Artificial Intelligenc

Research on the Early Recognition, Classification and Precision Intervention System of Diabetes Based on Artificial Intelligenc

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083379
Enrollment
Unknown
Registered
2024-04-23
Start date
2024-04-30
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

diabetes

Interventions

Part One: ungroup:None
Part Two: General lifestyle control group:All the groups were not classified, and the general lifestyle intervention was carried out according to the guidelines.
Part Two: Precise classification of individual intervention group:The classification and intervention were carried out in Beijing Hospital and Beijing Tiantan Hospital Affiliated to Capital Medical Un
The second group is the moderate-risk group of obesity and insulin deficiency, and intensive lifestyle intervention is recommended by reference to the 2020 edition of the Chinese Guidelines for the pr
At least reduce the total daily calories in your diet 400-500kcal (1kcal=4.184kJ), overweight or obese people should reduce 500-750kcal
(3) Saturated fatty acid intake accounted for less than 30% of total fatty acid intake
The total amount of salt per person per day should not exceed 5g
? Moderate intensity physical activity should be maintained at least 150min/ week
The third group is the high-risk insulin resistance type group, which recommends lifestyle +500mg tid metformin intervention.
Part Three: ungroup:None

Sponsors

Beijing hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Part Two and Part Three: (1) Diabetes high-risk groups diagnosed by the identification model; (2) Age 18-75 years old; (3) Sign informed consent and take the test voluntarily;

Exclusion criteria

Exclusion criteria: Part Two and Part Three: (1) Incomplete data; (2) critically ill patients; (3) Patients with mental illness who cannot sign informed consent; (4) Refusing to participate in the survey; (5) can not use artificial intelligence equipment or life can not take care of themselves.

Design outcomes

Primary

MeasureTime frame
Glycosylated hemoglobin;Fasting blood glucose;Postprandial blood glucose;weight;Blood pressure;Fasting insulin;triglyceride;cholesterol;Low density lipoprotein cholesterol;High density lipoprotein cholesterol;BMI;Fasting c-peptide;Postprandial C-peptide;Postprandial insulin;

Secondary

MeasureTime frame
Waist-hip circumference;urine protein;urine acetone bodies;Urinary nitrite;glutamic-pyruvic transaminase;glutamic oxalacetic transaminase;total bilirubin;alkaline phosphatase;urea nitrogen;creatinine;height;pulse;

Countries

China

Contacts

Public ContactGuo lixin

Beijing hospital

glx1218@163.com+86 139 0131 7569

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026