- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05768022
Origin to Insertion Kinesio Tapping vs Non-Directional Kinesio Tapping on Quadriceps Peak Torque
March 12, 2023 updated by: Mohamed Moustafa Mohamed Ahmed, University of Jazan
Origin to Insertion Kinesio Tapping vs Non-Directional Kinesio Tapping on Quadriceps Peak
This study was conducted to investigate the effect of kinesio tapping on electrical activity and peak torque of quadriceps during concentric and eccentric muscle contraction were carried out in the motion analysis Laboratory.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A Pretest posttest control group design was used to. Two hundred normal subjects of both sexes were recruited.
Subjects were randomly assigned into two groups of equal number.
- Cura Kensio-tapping group: consisted of 100 subjects (females and males) will receive kinesio taping from origin to insertion on the superficial muscles of Quadriceps femoris (vastus medialis (VM), vastus lateralis (VL), rectus femoris (RF).
- Placebo-Group: consisted of 100 subjects (females and males) will receive placebo kinesio taping across quadriceps.
Study Type
Interventional
Enrollment (Actual)
200
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 Locations
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Gizan
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Jazan, Gizan, Saudi Arabia, 45142
- Jazan University
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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
22 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age must be ranged from 22-30 years.
- Body mass index must be ranged from 20-24.9 kg/m².
Exclusion Criteria:
- Knee or quadriceps disorders preventing physical stress.
- Cardiovascular or neurological problems.
- Athletic subjects.
- Smokers.
- Heavy caffeine intake subjects.
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Cura kinesio-taping
100 subjects (females and males) will receive kinesio taping from origin to insertion on the superficial muscles of Quadriceps femoris (VM,VL, RF).
|
Cura tapes, a cotton strip with an acrylic adhesive.
allows for unidirectional elasticity up to 60% beyond its resting length.
|
Placebo Comparator: Placebo
100 subjects (females and males) will receive placebo kinesio-taping across quadriceps.
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placebo taping
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Peak Torque Measurement 1
Time Frame: Before tapping.
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The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
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Before tapping.
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Peak Torque Measurement 2
Time Frame: After the application of tapping by 10 minutes
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The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
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After the application of tapping by 10 minutes
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Peak Torque Measurement 3
Time Frame: 24 hours after tapping.
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The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
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24 hours after tapping.
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Peak Torque Measurement 4
Time Frame: 72 hours After tapping
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The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
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72 hours After tapping
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Peak Torque Measurement 5
Time Frame: 5 days after removal of tapping b
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The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
|
5 days after removal of tapping b
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
February 1, 2023
Primary Completion (Actual)
February 26, 2023
Study Completion (Actual)
March 5, 2023
Study Registration Dates
First Submitted
February 18, 2023
First Submitted That Met QC Criteria
March 12, 2023
First Posted (Actual)
March 14, 2023
Study Record Updates
Last Update Posted (Actual)
March 14, 2023
Last Update Submitted That Met QC Criteria
March 12, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 91177
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.
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