Assessment and Digital-health Based Intervention on Subclinical Organ Damage and Cardiovascular Risk in Chinese

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShanghai 10th People's Hospital

About this trial

To comprehensively evaluate subclinical organ damage of Chinese adults and its association with future cardiovascular disease and events.

To observe the significance of intervention based on digital health in preventing the onset and/or progression of subclinical organ damage and cardiovascular disease and events.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

aged 18 years or older

willing to participate the study and sign informed consent

available for long-term follow-up

Disqualifiers

severe heart disease (NYHA IV)

stage 4 or 5 CKD

malignant tumors or with life expectancy less than 5 years

stroke within 3 months

Trial population

All healthy subjects having cardiovascular health check-up and patients with cardiovascular diseases in the cardiovascular research clinic of our hospital are eligible for this study

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

composite endpoint of cardiovascular events

rate of subject with myocardial infarction, stroke, heart failure, cardiovascular death

Time frame
5 years

Secondary outcomes

1

Individual cardiovascular events

rate of subject with individual components of composite endpoint

Time frame
5 years
2

all cause mortality

rate of death

Time frame
5 years
3

New on-set subclinical organ damage

Rate of subject with new on-set subclinical organ damage. Subclinical organ damage evaluated contains heart (left ventricular hypertrophy and diastolic dysfunction), kidneys (chronic kidney disease, microalbuminuria), vasculature (arterial stiffness, carotid plaque, intima-media thickness), and eye background (arteriosclerotic retinopathy).

Time frame
5 years

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: