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A digital cohort study of cardiometabolic health in older adults

Digital Intelligence for Cardiometabolic Health Management in Older Adults: a community-based prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096478
Enrollment
Unknown
Registered
2025-01-24
Start date
2025-01-27
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Cardiometabolic diseases, mainly including hypertension, type 2 diabetes mellitus, hyperlipidemia, ischemic heart disease, cerebrovascular disease, etc.

Interventions

Elderly patients with cardiometabolic diseases:Cardiometabolic risk factors and other possible risk factors

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 60-80 years old; 2.A resident of the community for a period exceeding six months; 3.A history of at least one cardiometabolic disease, including hypertension, type 2 diabetes mellitus, hyperlipidemia, ischemic heart disease and cerebrovascular disease, has been previously diagnosed; 4.The patient is able to utilise smartphones and mobile phone applications (apps) with proficiency, either independently or with the assistance of family members; 5.The patients themselves have elected to participate in the study and have signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Excluding those who have suffered from cardiovascular events in the past year or have been hospitalised for any reason in the past six months; 2.The presence of comorbid active malignant tumours, severe autoimmune diseases, or long-term use of hormones, immunosuppressants, or biologically targeted therapies; 3.Neurological diseases or serious mental illnesses (e.g., mania, schizophrenia) that result in dementia/aphasia or intellectual disabilities that impede the ability to cooperate with enumerators in the completion of data collection and communication tasks; 4.Long-term residence in a care facility for the elderly. e. The presence of skin soft tissue lesions, fractures, or aberrant vascular supply (vascular occlusion or thrombosis, trauma) in both upper extremities may impact the ability to wear or accurately measure the bracelet; 5.Inability to utilise the device or mobile phone application correctly during the screening period, or to record or assess as required; 6.Various reasons for which the subject is unable to wear the bracelet for the requisite duration; 7.Any additional conditions that the investigator deems unsuitable for enrolment;

Design outcomes

Primary

MeasureTime frame
Major adverse cardiovascular events;

Secondary

MeasureTime frame
Sarcopenia;Fall;Dementia;Number of unplanned hospitalisations;Death;

Countries

China

Contacts

Public ContactJiang Hua

Shanghai East Hospital

huajiang2013@tongji.ed+86 21 38804518

Outcome results

None listed

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