- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06620224
Exploring the Impact of VR-based Acupuncture Treatment on Patient Experience and Doctor-patient Interaction.
September 30, 2024 updated by: China Medical University Hospital
Exploring the Impact of Virtual Reality-based Traditional Chinese Acupuncture Treatment on Patient Experience and Doctor-patient Interaction.
Develop and establish a virtual reality acupuncture system, and introduce the technology acceptance model to systematically explore the impact of acupuncture treatment effectiveness and its related medical experience and doctor-patient interaction
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Whether it's Western medicine's surgical treatment or traditional Chinese medicine's acupuncture and acupotomy treatment, for patients preparing to undergo invasive treatment, pre-treatment explanations can improve patient compliance and reduce patient anxiety about disease treatment.
The application of virtual reality systems in the medical field is mostly in preoperative training and medical education, while in the field of traditional Chinese medicine, it focuses on acupuncture teaching, with less evaluation of explanations before acupuncture treatment.
Therefore, this study will develop and establish a virtual reality acupuncture system, and introduce the technology acceptance model to systematically explore the impact of acupuncture treatment effectiveness and its related medical experience and doctor-patient interaction
Study Type
Interventional
Enrollment (Estimated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yu-Chen Lee, M.D.,PhD
- Phone Number: 886-975-682023
- Email: 005167@tool.caaumed.org.tw
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- general public and people see a doctor in the department of acupuncture
Exclusion Criteria:
- participant refusing the intervention of the virtual reality
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
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Participant wear the Virtual Reality system
Establish a virtual reality acupuncture system, and introduce the technology acceptance model to systematically explore the effectiveness of acupuncture treatment and its related impact on the patient experience and doctor-patient interaction,
|
we only use single group in this study, before the acupuncture treatment, let the participant wear the virtual reality to realize the course of the acupuncture treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Technology Acceptance Model
Time Frame: Immediately
|
Measured by the 5-point likert scale:very agree(5), agree(4), neither agree nor disagree(3), disagree(2), very disagree(1)
|
Immediately
|
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 (Estimated)
September 20, 2024
Primary Completion (Estimated)
September 20, 2024
Study Completion (Estimated)
August 31, 2025
Study Registration Dates
First Submitted
September 23, 2024
First Submitted That Met QC Criteria
September 30, 2024
First Posted (Actual)
October 1, 2024
Study Record Updates
Last Update Posted (Actual)
October 1, 2024
Last Update Submitted That Met QC Criteria
September 30, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CMUH113-REC1-147
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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