Analyze the Comparison of the Effectiveness of Kinesio ®and Dynamic Taping for De Quervain's Teno… (NCT07062276) | Clinical Trial Compass
TerminatedNot Applicable
Analyze the Comparison of the Effectiveness of Kinesio ®and Dynamic Taping for De Quervain's Tenosynovitis
Stopped: The COVID epidemic broke out shortly after the project started, and the number of cases coming to the hospital dropped sharply. Finally, the research project had to be terminated because it expired.
Taiwan8 participantsStarted 2022-06-30
Plain-language summary
\_De Quervain's tenosynovitis is inflammation and swelling of the tendon caused by repetitive thumb movements. In severe cases, the tendon sliding is limited, resulting in limited joint range of motion and affecting the quality of life. Kinesio ®can effectively improve pain, edema, and assist functional movements. The elasticity of the patch creates wrinkles to relax the extensor pollicis brevis and the abductor longus muscle of the thumb. The dynamic tape is a new type of treatment. The material has high resilience. Its purpose is to help muscles and tissues absorb external forces and reduce tissue energy consumption. By adjusting the human motor control mode, the work of injured tissues can be reduced, thereby improving the discomfort of sports injuries , accelerating the recovery of injured tissues and reducing the load of the extensor pollicis brevis tendon and the abductor pollicis longus tendon to assist the two tendons in their work. However, in the past, there was no dynamic taping applied to the study of De Quervain's tenosynovitis, and no dynamic taping and Kinesio ® applied to the study of De Quervain's tenosynovitis.
Who can participate
Age range
20 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* An outpatient case of De Quervain's tenosynovitis referred by a rehabilitation physician.
* Symptoms need to last for more than 1 month.
* The case did not administer any medications and did not receive any rehabilitation treatment before being transferred to the occupational therapy department.
* The case will not have any uncomfortable reaction to Kinesio ® and dynamic taping.
* The case or the main caregiver can understand and cooperate with the relevant instructions of the research.
* Those who are willing to sign the consent form after fully understanding this research
Exclusion Criteria:
* Medical personnel have identified medical problems that may affect the test
* Authors of stroke recurrence or epilepsy during the intervention
* Participate in other experimental researches on rehabilitation efficacy during this research period
* Those who refuse to sign the subject's consent form
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Basic Demographic Information
Timeframe: Before the intervention.
2
The Patient-Rated Wrist Evaluation(PRWE)
Timeframe: Change from Baseline and after intervention 24hours
3
JAMAR® dynamometer
Timeframe: Change from Baseline and after intervention immediately
Trial details
NCT IDNCT07062276
SponsorTaipei Medical University Shuang Ho Hospital