Patients With Type 2 Diabetes
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Diabetes Mellitus Type 2. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Taiwan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Cohort Study of Patients With Type 2 Diabetes
Overview
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.
Primary outcome measures
- Changes in nutritional status and physical function (including dietary habits, body composition, and grip strength) [Time frame: Everytime after physician's appointment(Usually 3 months).]
Eligibility criteria
Inclusion criteria
- Adults aged 18 or older.
- Patients diagnosed with type 2 diabetes (based on medical history, diagnostic code, or use of hypoglycemic medication).
- Participants are willing to participate in the study and have signed the consent form.
- Participants are able to complete basic assessments (e.g., height, weight, waist circumference, grip strength, body composition, etc.).
Exclusion criteria
- Individuals who cannot understand the study content.
- Individuals who cannot cooperate with relevant assessments.
- Other individuals who are clinically deemed unsuitable for participation by the project leader.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Taiwan · 1 center
- National Taiwan University Hospital — Taipei
Identifiers
NCT: NCT07245082 · 202507201RINE