- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05106543
Immediate Effect Of Kinesiological Taping
Immediate Effect Of Kinesiological Taping On Functionality In Hemiplegic Patients
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Istanbul, Turkey
- Okan University
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Istanbul, Turkey
- Immediate Effect Of Kinesiological Taping On Functionality In Hemiplegic Patients
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- agree to participate in the study after detailed information about the study,
- to have sufficient cognitive functions, to be diagnosed with hemiplegia by a specialist physician,
- to be 18 years of age or older
Exclusion Criteria:
- Diagnosis of other neurological diseases (Parkinson's, Multiple Sclerosis, etc.),
- cancer other than hemiplegia, heart failure, surgery in the area to be applied,
- vascular problems in the lower extremity,
- chronic kidney failure,
- infection.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: kinesiologic tape
first group of 20 people (experimental group) T max branded kinesiology tape was applied to both M. Quadriceps Femoris and M. Gastrocnemius muscles of the experimental group. Timed get up and go test was applied to evaluate functionality. All evaluations were applied before taping, immediately after taping and 45 minutes after taping. Patients in both groups were asked not to have their tapes removed until the 4th day. Apart from routine physical therapy methods and taping, no other treatment was applied to the patients. |
Kinesiological Taping
|
Placebo Comparator: patch tape
second group of 20 people (control group) Roll branded patch tape was applied to both M. Quadriceps Femoris and M. Gastrocnemius muscles of the control group. Timed get up and go test was applied to evaluate functionality. All evaluations were applied to both groups before taping, immediately after taping and 45 minutes after taping. Patients in both groups were asked not to have their tapes removed until the 4th day. Apart from routine physical therapy methods and taping, no other treatment was applied to the patients. |
Kinesiological Taping
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Immadiate Effect Of Kinesiological Taping
Time Frame: 4 days
|
With a computerized randomization system, 40 people, 20 of whom we applied kinesiology taping in the first group (study group), and the second group of 20 people (control group), were determined. T max branded kinesiology tape was applied to both M. Quadriceps Femoris and M. Gastrocnemius muscles of the experimental group. Roll branded plaster tape was applied to both M. Quadriceps Femoris and M. Gastrocnemius muscles of the control group. Timed get up and go test was applied to evaluate functionality. All evaluations were applied to both groups before taping, immediately after taping and 45 minutes after taping. Patients in both groups were asked not to have their tapes removed until the 4th day. All patients were re-evaluated on the 4th day. Apart from routine physical therapy methods and taping, no other treatment was applied to the patients. |
4 days
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: emine atici, pt phd, Okan University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BaskentU 1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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