China Diabetes Cognitive Dysfunction Early Diagnosis and Intervention Study (China-DECODE Study)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age45+
SponsorThe Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

About this trial

Type 2 diabetes (T2D) and dementia are both diseases with increasing incidence and prevalence globally, leading to substantial economic burdens for families and society. Notably, diabetes significantly increases the risk of cognitive dysfunction, which is classified into preclinical stage, mild cognitive impairment and dementia based on the disease severity. Cognitive dysfunction is a critical contributor to disability and mortality in elderly diabetes patients. Early diagnosis and intervention are crucial for delaying disease progression, enhancing treatment efficacy, and mitigating the impact of dementia. Currently, research and clinical management of cognitive dysfunction in individuals with diabetes are in their infancy, characterized by limitations such as single-center studies, limited sample sizes, inconsistent diagnostic criteria, and insufficient data sharing. Consequently, clinical diagnosis and treatment strategies are underdeveloped, medical staff's related knowledge is lacking, and potential therapeutic targets remain unexplored. In view of these problems and shortcomings, the population cohort study is supposed to be carried out based on accurate diagnosis and constructed the high standard information and sample bank. The study will establish the standard and quality system of T2D with cognitive dysfunction cohort study (unified standards and norms). The study will integrate the standard biological samples stratified acquisition function module (homogeneity and precision) of cognitive dysfunction in T2D, and complete the construction of biological samples bank and clinical diagnosis and treatment information database. The study will apply and develop brain structural and functional imaging technology to support precision diagnosis of cognitive dysfunction in T2D.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age ≥45 years;

Type 2 diabetes diagnosed according to the American Diabetes Association criteria;

Willingness and ability to complete systematic neuropsychological tests;

Understanding of the research procedures and methods, potential benefits and risks of the trial, and sign written informed consent.

Disqualifiers

Fewer than 6 years of education;

Left-handedness;

Dementia;

Acute metabolic complications such as diabetic ketoacidosis, hyperglycaemic hyperosmolar state and hypoglycaemic coma within the previous 3 months;

Trial population

This study is a dynamic prospective cohort study.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Naturalistic observation

    Other intervention

    Naturalistic observation

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Prevalence, incidence of cognitive dysfunction in type 2 diabetes

Prevalence, incidence of mild cognitive impairment in type 2 diabetes

Time frame
From 2016 to 2034
2

Risk factors for cognitive dysfunction in type 2 diabetes, such as diabetes duration, poor glycemic control, hypertension, obesity, dyslipidemia, and active inflammation, et al.

Risk factors for the occurrence and progression of mild cognitive impairment in type 2 diabetes, such as diabetes duration, poor glycemic control, hypertension, obesity, dyslipidemia, and active inflammation, et al.

Time frame
From 2016 to 2034
3

Biomarkers of cognitive dysfunction in type 2 diabetes

Diagnostic biomarkers, predictive biomarkers, and prognostic biomarkers of cognitive dysfunction in type 2 diabetes

Time frame
From 2016 to 2034
4

Glycemic control targets for cognitive dysfunction in type 2 diabetes

Glycemic control targets (including glycated hemoglobin, glycemic fluctuations and hypoglycemic events) for slowing or reversing disease progression of cognitive dysfunction in type 2 diabetes.

Time frame
From 2016 to 2034

Secondary outcomes

Other outcomes

Sponsors and contacts

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