Influence of Kinesio Tapping on Quadriceps Muscle Peak Torque and Bioelectrical Activity After Meniscectomy

April 12, 2023 updated by: Mohamed Moustafa Mohamed Ahmed, University of Jazan

Influence of Kinesio Tapping on Quadriceps Muscle Peak Torque and Bioelectrical Activity After Arthroscopic Partial Meniscectomy (RTC)

A Pretest post-test control group design will be used to investigate the effect of kinesio taping on electrical activity and peak torque of the quadriceps femoris muscle during concentric and eccentric contraction after arthroscopic partial meniscectomy (APM) surgery.

Study Overview

Status

Completed

Conditions

Detailed Description

Fifty patients after APM of any knee of both sexes will participate in this study after signing a written informed consent form approved.

from the ethical committee of Jazan University. They are selected according to the following Inclusion criteria:

  1. All performed APM only without any other knee injury.
  2. Finished the period of hospital stay (6-8 weeks)
  3. Their age ranged from 20-40.
  4. Their Body mass index ranged from 20-24.9 kg/m². 2- The subjects will be excluded from the study if they had one of th e following exclusion criteria: a- Knee or quadriceps disorders preventing physical stress. b- Subjects with cardiovascular or neurological problems. c- Smokers. d- Heavy caffeine intake subjects. 3- The subjects will be randomly assigned into two groups of equal numbers. Group A (Study) consisted of 66 subjects who will receive kinesio-taping from origin to insertion on the superficial muscles of the Quadriceps femoris (QF) (Vastus Medialis (VM), Vastus Lateralis (VL), Rectus Femoris (RF)). - Group B (Control) consisted of 66 subjects who will receive a placebo kinesio-taping across quadriceps. Anthropometric measures including "weight and height" and body. mass index (BMI) will be measured for all subjects in the first meeting before starting the evaluative procedures. All subjects were asked to shave the hair of their thigh before starting the evaluative procedure using blades, which was essential to prevent artifact during EMG evaluation and to facilitate the adherence of the tape to the skin. Bioelectrical activity and peak torque of quadriceps muscle of the lower extremity that had APM will be measured. The evaluation will be carried out before tapping, and then after the application of tapping for 10 minutes.

Study Type

Interventional

Enrollment (Actual)

132

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

20 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Clinical diagnosis only with arthroscopic partial meniscectomy
  2. Must be finished a period of hospital stay (6-8 weeks)
  3. Must have body mass index ranged from 20-24.9 kg/m².

Exclusion Criteria:

a. Knee or quadriceps disorders preventing physical stress. b- Cardiovascular or neurological problems. c- Smokers d- 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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Cura kinesio-taping
consisted of 25 subjects who will receive kinesio-taping from origin to insertion on the superficial muscles of Quadriceps femoris (QF) (Vastus Medialis (VM), Vastus Lateralis (VL), Rectus Femoris (RF)
Cura tapes, a cotton strip with an acrylic adhesive. allows for unidirectional elasticity up to 60% beyond its resting length will be applied on origin to insertion on the superficial muscles of Quadriceps femoris (QF) (Vastus Medialis (VM), Vastus Lateralis (VL), Rectus Femoris (RF)
Placebo Comparator: Placebo kinesio-taping
consisted of 25 subjects who will receive placebo kinesio-taping across quadriceps.
Placebo kinesiotaping

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Peak muscle torque
Time Frame: 1. Baseline: before tapping 2. after10 minutes of Cura kinesio-taping.
Peak torque of the quadriceps femoris muscle during concentric and eccentric contraction after arthroscopic partial meniscectomy (APM) surgery using Biodex system
1. Baseline: before tapping 2. after10 minutes of Cura kinesio-taping.
Bioelectrical activity of quadriceps muscle
Time Frame: 1. Baseline: before tapping 2. after10 minutes of Cura kinesio-taping.

bioelectrical activity of the three quadriceps muscle heads will be measured. All subjects were asked to shave the hair of their thigh before starting.

the evaluative procedure using blades, which was essential to prevent artifact during EMG evaluation and to facilitate the adherence of the tape to the skin

1. Baseline: before tapping 2. after10 minutes of Cura kinesio-taping.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Mohamed M Ahmed, Assistant Professor, Jazan University

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 6, 2023

Primary Completion (Actual)

February 26, 2023

Study Completion (Actual)

March 5, 2023

Study Registration Dates

First Submitted

December 16, 2022

First Submitted That Met QC Criteria

February 3, 2023

First Posted (Actual)

February 6, 2023

Study Record Updates

Last Update Posted (Actual)

April 18, 2023

Last Update Submitted That Met QC Criteria

April 12, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 1147

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

I will share the data on request.

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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