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Construction of a model for preoperative functional assessment with wearable devices for medical use comparing cardiopulmonary combined exercise testing: a volunteer study

Construction of a model for preoperative functional assessment with wearable devices for medical use comparing cardiopulmonary combined exercise testing: a volunteer study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085588
Enrollment
Unknown
Registered
2024-06-13
Start date
2024-06-15
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

None

Interventions

group 1:Cardiopulmonary exercise test followed by a six-minute walk test
group 2:Six-minute walk test followed by cardiopulmonary exercise test

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Those who voluntarily participate in this trial and allow de-privatization of scientific data for publication in professional journals or platforms; between the ages of 20-45 years old; of any gender; who are in good health, have not undergone any surgery or long-term medication, and who are able to provide a physical examination report issued within the last 2 years at a qualified and certified physical examination institution/hospital.

Exclusion criteria

Exclusion criteria: Cardiac arrhythmia, including but not limited to ventricular premature beats, atrial premature beats, etc.; deliberate concealment of true medical conditions; long-term smoking, alcoholism; long-term high-intensity sports and fitness; long-term poor living or working habits, such as sedentary, long standing (for example, after removing 8 hours of sleep, the remaining time more than 2/3 of the time is sedentary or long standing, which is considered as a bad habit); important joints or spinal injuries history; concurrent participation in other clinical trials.

Design outcomes

Primary

MeasureTime frame
peak oxygen consumption;

Secondary

MeasureTime frame
anaerobic threshold;Carbon dioxide ventilation equivalent slope;

Countries

China

Contacts

Public ContactXu Zhenzhen

Peking University First Hospital

derekmerrr@126.com+86 188 1159 1915

Outcome results

None listed

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