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

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

    • Gizan
      • Jazan, Gizan, Saudi Arabia, 45142
        • Jazan University

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.
placebo taping

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Peak Torque Measurement 1
Time Frame: Before tapping.
The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
Before tapping.
Peak Torque Measurement 2
Time Frame: After the application of tapping by 10 minutes
The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
After the application of tapping by 10 minutes
Peak Torque Measurement 3
Time Frame: 24 hours after tapping.
The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
24 hours after tapping.
Peak Torque Measurement 4
Time Frame: 72 hours After tapping
The peak torque of quadriceps muscle of dominant lower limb was measured using Biodex system 830-200 Isokinetic dynamometer.
72 hours After tapping
Peak Torque Measurement 5
Time Frame: 5 days after removal of tapping b
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.

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

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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