Validation of a device for remote pulse assessment in Traditional Chinese Medicine

Validation Study of an Assistive Pulse Data Collection Device

Phase 1 Interventional The Hong Kong Polytechnic University · NCT06974227

This study is testing a new device that records pulse information to see if it can help Traditional Chinese Medicine practitioners assess patients remotely.

Quick facts

PhasePhase 1
Study typeInterventional
Enrollment30 (estimated)
Ages18 Years to 65 Years
SexAll
SponsorThe Hong Kong Polytechnic University Academic / other
Locations1 site (Hong Kong)
Trial IDNCT06974227 on ClinicalTrials.gov

What this trial studies

This study aims to validate an Assistive Pulse Data Collection Device (APDC) designed to capture and regenerate pulse features for remote assessment in Traditional Chinese Medicine (TCM). Participants aged 18-65 with a specific BMI range will have their pulse recorded by the device, which will then be evaluated by Chinese Medicine Practitioners (CMPs) for accuracy and reliability. The study will collect feedback from both CMPs and subjects to refine the device's functionality and ensure it accurately reflects the subjects' pulse characteristics.

Who should consider this trial

Good fit: Ideal candidates for this study are healthy male and female subjects aged 18-65 with a BMI between 18.5 and 22.5 kg/m2.

Not a fit: Patients with a dorsally located radial artery will not benefit from this study due to exclusion criteria.

Why it matters

Potential benefit: If successful, this device could enhance remote diagnostic capabilities in TCM, improving patient access to healthcare.

How similar studies have performed: While the approach of using technology for pulse assessment is innovative, similar studies in remote diagnostics have shown promise, indicating potential for success.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age 18-65 years
2. BMI 18.5-22.5 kg/m2
3. Willing to give informed consent

Exclusion Criteria:

1\. dorsally located radial artery

Where this trial is running

Hong Kong

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Healthy Male and Female Subjectsmachinepulsewave formTCM
Last reviewed 2026-06-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.