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Recruiting NCT06861283

Development and Validation of a Digital Twin-based Clinical Research System (X Town Stage I)

Observational Chronic Disease

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: Chronic Disease. 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
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Chronic diseases, characterized by their prolonged duration and slow progression, have emerged as predominant contributors to global morbidity and mortality. The investigators have developed a digital twin-based clinical research system (termed X Town) for chronic diseases, to predict clinical outcomes under various interventions. In this study, the investigators aim to evaluate the reliability of the developed digital twin-based clinical research system in predicting short-term clinical outcomes via virtual and real-world clinical studies.

Primary outcome measures

  • The agreement between the simulated short-term clinical outcomes in the virtual clinical studies and the real-world short-term clinical outcomes in the real-world clinical studies [Time frame: Within 3 months]

Eligibility criteria

Inclusion criteria

  • Age≥18 years old
  • Receiving care at a community health service centre
  • Able to understand and comply with the study procedures
  • Agrees to participate in the study and signs the informed consent form

Exclusion criteria

  • Patients with severe mental illness
  • Patients expected to be unable to complete follow-ups

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
Other

Study locations

China · 1 center
  • Shanghai Health and Medical Center — Wuxi

Identifiers

NCT: NCT06861283 · 2025-KY-025(K)

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗