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Study identifier: NCT06974227 Synced from ClinicalTrials.gov · July 28, 2026
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Validation Study of an Assistive Pulse Data Collection Device

Condition: Healthy Male and Female Subjects  ·  Sponsor: The Hong Kong Polytechnic University

PhasePhase 1
Planned participants30
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

Background: Traditional Chinese Medicine (TCM) relies on pulse diagnosis, a subjective and complex method that is crucial for assessing patients' health status. The COVID-19 pandemic has disrupted healthcare delivery, highlighting the need for remote diagnostic tools. To address this, an Assistive Pulse Data Collection Device (APDC) has been developed to capture and regenerate pulse features for remote pulse assessment in TCM. Objective: This study aims to validate the accuracy and reliability of the APDC by assessing its agreement with Chinese Medicine Practitioners (CMPs) and collecting users' feedback. Intervention: The APDC consists of a radial artery viewing device, pulse collection device, and pulse regeneration device. Methods: Subjects will be recruited via social media and posters at the University. Inclusion criteria include age 18-65 years and BMI 18.5-22.5 kg/m2, while exclusion criteria include a dorsally located radial artery. Registered CMPs with at least 5 years of clinical experience will assess the pulse from both participants and the regenerated pulse by the device. Outcome Assessment: Agreement in pulse features between the subjects' real pulse and the pulse regeneration device will be assessed using a self-developed questionnaire, covering frequency, rhythm, wideness, and force. Quantitative and qualitative feedback from subjects and CMPs will be collected to assess their views on the APDC Device in terms of satisfaction, ease of use, and comfortabili…

This description comes directly from the study's public registry record.

Talk to the study team

WF Yeung, Ph.D  ·  852-27664151  ·  jerry-wf.yeung@polyu.edu.hik

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Locations (1)

The Hong Kong Polytechnic UniversityHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT06974227