Fascia Release Techniques Applied to Plantar Flexor Muscles and Acute Efficacy of Kinesio Taping

December 6, 2023 updated by: Dr. Öğr. Üyesi Ömer Şevgin, Uskudar University

Investigation of the Effects of Fascia Relaxation Techniques Applied to Plantar Flexor Muscles on Proprioception, Balance and Flexibility.

The aim of this study; The aim of this study is to examine the effects of kinesio taping technique and percussive massage technique applied to plantar flexor muscles on proprioception, balance and flexibility in healthy individuals.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The sample of the study will consist of healthy individuals who have not had any discomfort or surgical operation related to the lower extremity in the last 6 months. The demographic information of the individuals who agreed to participate in the study will be recorded and their written consent will be obtained. Participants will be divided into 2 groups as kinesio taping and Percussive Massage groups by randomization method. The dominant lower extremities of both groups will be applied. The Percussive Massage group will be applied to the posterior part of the sural fascia for 5 minutes, 3 times a week, including the plantar flexor muscles. In the kinesio taping group, taping will be done in accordance with the fascia correction technique, including the plantar flexor muscles, and it will be requested to stay for 3 days. Both groups will be evaluated before and after the application. Joint position sense test will be used to evaluate proprioception. In the evaluation of balance, the one-leg standing test will be considered. In the evaluation of flexibility; The flexibility of the hamstring, gastrocnemius, and plantar fascia will be examined. The Straight Leg Lift Test will be performed to look at the flexibility of the hamstring muscle. Pre- and post-intervention data were statistically analyzed and compared.

Study Type

Interventional

Enrollment (Actual)

40

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

  • Turkey
    • İstanbul
      • Umraniye, İstanbul, Turkey
        • Üsküdar Unıversıty

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

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Volunteering to participate in the study
  • Being between the ages of 18 and 60

Exclusion Criteria:

  • Injury or surgery involving the lower extremity in the last 6 months
  • having had an operation
  • Malignancy, aneurysm, fever, infection, fracture, osteoporosis, rheumatoid arthritis, diabetes,
  • coagulation disorder etc. myofascial release techniques are contraindicated
  • have ailments
  • Having any disorder that will affect balance

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
Experimental: kinesio taping
kinesio taping Technique: It is used to provide support to the joint range of motion and tissues. It has a wide range of uses for purposes such as correcting functional disorders, healing, protecting, reducing pain and inflammation. There are differences in cutting shapes according to the applied area and the target to be achieved.
Other: taping
Kinesio taping will be applied in accordance with the fascia correction technique, including the plantar flexor muscles, and it will be requested to stay on the skin for 3 days.
Experimental: percussive massage
Percussive Massage Technique: It is one of the instrument-assisted soft tissue mobilization techniques that emerged as a result of combining the effects of traditional massage and vibration therapy. With the mechanical oscillation effect that occurs in the Percussive Massage Technique, the muscle fiber is stimulated and an increase in reflex activity is observed.
Other: massage
Percussive Massage will be applied to the posterior part of the sural fascia, including the plantar flexor muscles, 3 times a week for 5 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Joint Position Sense Test
Time Frame: 1 weeks
The joint to be evaluated is passively brought to a certain angle and it is waited for 10 seconds so that the person can learn the position of the joint. The person is asked to actively bring the evaluated extremity back to this angle with the eyes closed. When the person completes the movement, the error degrees between the predetermined angles are determined and averaged.
1 weeks
One Leg Standing Test
Time Frame: 1weeks
Persons are positioned on one leg, with their hands on their waists, in front of a visually determined target. The foot to be tested is on the ground. The raised foot should not touch the leg on the ground. Time is kept from standing on one leg. The time taken until the foot held above touches the other leg or is lowered to the ground is recorded.
1weeks
Evaluation of Gastrocnemius Elasticity
Time Frame: 1 weeks
The person to be evaluated is positioned by extending his legs so that the heel is in contact with the wall, without bending the knees. The person is asked to pull the ankle towards himself without removing the heel from the wall. The distance between the person's thumb and the wall is measured and recorded.
1 weeks
Evaluation of Plantar Fascia Flexibility
Time Frame: 1 weeks
The person to be evaluated is positioned by extending his legs so that the heel is in contact with the wall, without bending the knees. The person is asked to pull the fingers back without separating the heel and metatarsal heads from the wall. The distance between the person's thumb and the wall is measured and recorded.
1 weeks
Straight Leg Lift Test
Time Frame: 1 weeks
The person to be evaluated lies in the supine position without bending their knees. The person is asked to raise the leg to be evaluated to the point where he or she will feel a stretching sensation in the back of the thigh, keeping the knee straight. It is recorded by measuring with a goniometer or digital inclinometer.
1 weeks

Collaborators and Investigators

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

Sponsor

Uskudar University

Investigators

  • Study Chair: Gamze MAMUR, Uskudar University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

September 1, 2023

Primary Completion (Actual)

October 1, 2023

Study Completion (Actual)

December 1, 2023

Study Registration Dates

First Submitted

August 17, 2023

First Submitted That Met QC Criteria

August 17, 2023

First Posted (Actual)

August 23, 2023

Study Record Updates

Last Update Posted (Estimated)

December 7, 2023

Last Update Submitted That Met QC Criteria

December 6, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • Uskudar61

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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