Patients With Type 2 Diabetes

Cohort Study of Patients With Type 2 Diabetes

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07245082

Enrollment

2000

Registered

2025-11-24

Start date

2025-10-09

Completion date

2028-08-21

Last updated

2026-09-15

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

Conditions

Diabetes Mellitus Type 2

Keywords

Obesity, Diabetic macular edema, diabetic kidney disease, Diabetic retinopathy, Nutritional status, Physical activity, Peripheral Arterial Occlusive Disease, Body composition, Metabolic Syndrome, Dynapenia

Brief summary

Diabetes mellitus

Detailed description

This study aims to establish both retrospective and prospective cohorts of patients with type 2 diabetes, enabling long-term follow-up of metabolic factors and related complications (such as cardiovascular disease, nephropathy, and neuropathy), as well as changes in nutritional status and physical function (including dietary habits, body composition, and grip strength). The goal is to identify risk factors that influence clinical outcomes and to provide evidence to support individualized treatment and integrated care strategies.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

1. Adults aged 18 or older. 2. Patients diagnosed with type 2 diabetes (based on medical history, diagnostic code, or use of hypoglycemic medication). 3. Participants are willing to participate in the study and have signed the consent form. 4. Participants are able to complete basic assessments (e.g., height, weight, waist circumference, grip strength, body composition, etc.).

Exclusion criteria

1. Individuals who cannot understand the study content. 2. Individuals who cannot cooperate with relevant assessments. 3. Other individuals who are clinically deemed unsuitable for participation by the project leader.

Design outcomes

Primary

Measure	Time frame
Changes in nutritional status and physical function (including dietary habits, body composition, and grip strength)	Everytime after physician's appointment(Usually 3 months).

Countries

Taiwan

Contacts

CONTACTChia-Wen Lu, Present Professor

biopsycosocial@gmail.com886-2-23123456

STUDY_CHAIRChia-Wen Lu, Present Professor

Department of Family Medicine, National Taiwan University Hospital

Outcome results