- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06834750
The Application of Kinesio Taping Technique in the Early Upper Limb Functional Activities Induction of Hemiplegic Patients After Stroke
March 20, 2025 updated by: The Fourth Affiliated Hospital of Zhejiang University School of Medicine
- To observe the inducing and promoting effect of kinesio taping technique on the recovery of upper limb function in early-stage stroke patients.
- To compare the different effects of kinesio tape and sports white tape on the induction and promotion of limb function in patients.
- To verify that kinesio taping technique is a safe and promotable technical means for stroke patients.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
120
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: Yinkai Cheng
- Phone Number: +86-15067757337
- Email: 505184583@qq.com
Study Locations
-
-
Zhejiang
-
Yiwu, Zhejiang, China, 310000
- 4th Affiliated Hospital, School of Medicine, Zhejiang University, China
-
Contact:
- Yinkai Cheng
- Phone Number: 15067757337
- Email: 505184583@qq.com
-
-
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
No
Description
Inclusion Criteria:
- The subjects voluntarily participated in the experiment and signed informed consent
- Diagnosed as a stroke patient
- No other major cardiovascular and cerebrovascular diseases
- First new stroke
- After evaluation by evaluators, subjects had Brunnstrom stage < 3
Exclusion Criteria:
- The subject's compliance was poor
- Increased muscle tone in the affected upper extremity
- Subjects with skin allergies
- Those who did not receive continuous treatment during the experiment
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: control group
The control group was pasted with sports white tape.
|
The control group was pasted with sports white tape (the pasting method was the same as above, replaced with sports white tape).
|
|
Experimental: experimental group
The experimental group received intramuscular patch therapy.
|
The application methods of kinesiology tape for the experimental group are as follows:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To observe the inducing and promoting effect of kinesio taping technique on the recovery of upper limb function in early-stage stroke patients.
Time Frame: Within 3 days of hospitalization, on the 1 day of discharge, one month after discharge
|
Fugl-Meyer Functional Score (FMA) is evaluated, and the higher the score, the stronger the motor function.
|
Within 3 days of hospitalization, on the 1 day of discharge, one month after discharge
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
To compare the different effects of kinesio tape and sports white tape on the induction and promotion of limb function in patients.
Time Frame: Within 3 days of hospitalization, on the 1 day of discharge, one month after discharge
|
Fugl-Meyer Functional Score (FMA) is evaluated, and the higher the score, the stronger the motor function.
|
Within 3 days of hospitalization, on the 1 day of discharge, one month after discharge
|
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)
April 1, 2025
Primary Completion (Estimated)
January 1, 2026
Study Completion (Estimated)
May 31, 2026
Study Registration Dates
First Submitted
February 14, 2025
First Submitted That Met QC Criteria
February 14, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 20, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KY-2024-244
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
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.