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Study on Cardiac Output Evaluation Based on Wearable Monitoring Data

N

Navy General Hospital, Beijing

Status

Not yet enrolling

Conditions

Cardiac Output

Treatments

Other: Exercise

Study type

Observational

Funder types

Other

Identifiers

NCT06938893
HZKY-PJ-2024-57

Details and patient eligibility

About

Based on the monitoring data of wearable devices, with cardiac output (CO) as the gold standard, this study intends to develop a non-invasive evaluation model of CO based on wearable data, and optimize the parameters to realize the cardiac capacity detection function in resting and exercise states on the wearable device.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Over 18 years old
  • Left ventricular ejection fraction (Left ventricular ejection fraction, LVEF) < 50%(200 subjects)
  • Left ventricular ejection fraction (Left ventricular ejection fraction, LVEF) ≥50% (100 subjects)
  • Able to use smart phones and operate wearable devices such as wristbands/watches

Exclusion criteria

  • Patients with pacemaker implantation
  • No smartphone
  • Currently participating in other clinical trials
  • Lactating women
  • Pregnant Women
  • Unable to run and ride due to personal physical and external reasons (subjects participating in the exercise state cardiac output model study)
  • Physical examination results in the past year have clear cardiovascular, metabolic, bone and joint related diseases that have exercise risk, or have diseases and related potential health risks confirmed by the self-examination form of physical status before exercise (participants in the exercise state cardiac output model study)
  • No informed consent was obtained

Trial contacts and locations

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Central trial contact

Yutao Guo

Data sourced from clinicaltrials.gov

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