Visualization Engineering Platform for TCM Pulse Diagnosis - Pulse Diagnosis Based on Federated Learning to Diagnose Slippery and Choppy and Other Pulses Waveform Image Features to Assist in the Study of TCM Pathological Logic Analysis

December 2, 2022 updated by: China Medical University Hospital
The diagnoses processes of Traditional Chinese Medicine (TCM) focus on the following four main types of diagnoses methods consisting of inspection, olfaction, inquiry, and palpation. The most important one is palpation also called pulse diagnosis which is to measure wrist artery pulse by TCM doctor's fingers to detect patient's health state. The pulse diagnosis has three parts, namely 'Chun', 'Guan' and 'Chy', with the location. Wrist measurements correspond to different parts of the body's organs. In this project, it is to classify pulse types by using specialized pulse measuring instruments. The measured pulse wave (Measured Pulse Wave, MPW) was segmented into arterial pulse wave curves (APWC) by the image suggestion method. The research object of this project is to collect and group patients diagnosed by traditional Chinese medicine practitioners, namely slippery pulse, choppy pulse group and normal pulse control group, with at least 80 cases for each group. The research purpose of this project is mainly to carry out the visualization engineering platform of TCM pulse diagnosis - based on the pulse diagnosis of federated learning to diagnose the pulse waveform image features such as slippery pulse and choppy pulse to provide auxiliary TCM pathological logic analysis research and back-end cross-federal learning of TCM pulse diagnosis Implementation of the node system. In other words, it is expected that the pulse wave characteristics measured by TCM physicians who cooperate with experts in the field can be collected from many TCM pulse diagnosis federated learning nodes, and analyzed by the Multiple-Expert Repertory Grid Elicitation (MERGE) method. Finally, the artificial intelligence model based on FL is trained to carry out TCM pathological logic analysis and related research. The results will be provided to TCM physicians as an important reference to assist clinical diagnosis.

Study Overview

Status

Recruiting

Study Type

Observational

Enrollment (Anticipated)

240

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North District
      • Taichung, North District, Taiwan, 40447
        • Recruiting
        • China Medical University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

outpatient

Description

Inclusion Criteria:

  1. Already sign test consent permit.
  2. More than 20-year-old.

Exclusion Criteria:

1. There is a wound or inflammation at the wrist skin measurement.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Other
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Slippery Pulse
Time Frame: 30 minutes in duration
The purpose of the study was to establish a scientific slippery pulse diagnosis system
30 minutes in duration

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

December 1, 2022

Primary Completion (Anticipated)

September 1, 2024

Study Completion (Anticipated)

September 1, 2024

Study Registration Dates

First Submitted

November 20, 2022

First Submitted That Met QC Criteria

November 20, 2022

First Posted (Actual)

November 29, 2022

Study Record Updates

Last Update Posted (Estimate)

December 6, 2022

Last Update Submitted That Met QC Criteria

December 2, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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