Ankle Kinesio Taping vs Mulligan's Mobilization With Movement

November 14, 2018 updated by: Murat TOMRUK, Dokuz Eylul University

Comparison of the Effects of Kinesio Taping and Mulligan's Mobilization With Movement on Balance, Muscle Strength and Flexibility in Healthy Ankles

The aim of the study is to compare the effects of Kinesio taping and Mulligan's mobilization with movement technique on balance, muscle strength and flexibility in healthy ankles . Patients will randomly be divided into 4 groups: Kinesio taping (KT) group, sham Kinesio taping (SKT) group, Mulligan's mobilization with movement (MWM) group and sham mobilization with movement (SMWM) group . Kinesiotape will be applied both ankles as "Correction technique" in KT group, 'Posterolateral glide mobilization with movement' will be applied 10 times to both ankles in MWM group. The evaluations will be repeated after waiting 45 minutes to reveal the effects of Kinesio taping and Mulligan mobilization with movement.

Study Overview

Study Type

Interventional

Enrollment (Actual)

80

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

      • İzmir, Turkey
        • Dokuz Eylül 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

18 years to 35 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Age between 18-35
  • Healthy individuals
  • Able to read, write and understand Turkish
  • willing and able to attend study

Exclusion Criteria:

  • Any neurological, musculoskeletal or vascular disease in any of the lower extremity.
  • Previous history of surgery in any of the lower extremity.
  • Mental and cognitive disorders that would seriously affect cooperation

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
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Kinesio-taping
Kinesiotape will be applied both ankles.
Kinesiotape will be applied both ankles as "Correction technique".
EXPERIMENTAL: Mulligan's mobilization with movement
'Posterolateral glide mobilization with movement' will be applied both ankles.
'Posterolateral glide mobilization with movement' will be applied 10 times to both ankles.
SHAM_COMPARATOR: Sham Kinesio-taping
Sham kinesio-taping technique will be applied both ankles.
Sham Kinesio-taping technique will be applied both ankles.
SHAM_COMPARATOR: Sham Mulligan's mobilization with movement
Sham Mulligan's mobilization with movement will be applied both ankles.
Sham Mulligan's mobilization with movement technique will be applied both ankles.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in balance
Time Frame: Before intervention and 45 minutes after the intervention
Change in balance will be measured by using Biodex Balance System.
Before intervention and 45 minutes after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in muscle strength
Time Frame: Before intervention and 45 minutes after the intervention
Change in muscle strength will be assessed by using hand-held dynamometer.
Before intervention and 45 minutes after the intervention
change in flexibility
Time Frame: Before intervention and 45 minutes after the intervention
Change in flexibility will be assessed by weight-bearing lunge test
Before intervention and 45 minutes after the intervention
change in range of motion
Time Frame: Before intervention and 45 minutes after the intervention
Change in range of motion will be assessed by using electronic gonyometer
Before intervention and 45 minutes after the intervention

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)

August 6, 2018

Primary Completion (ACTUAL)

October 13, 2018

Study Completion (ACTUAL)

October 31, 2018

Study Registration Dates

First Submitted

July 27, 2018

First Submitted That Met QC Criteria

August 2, 2018

First Posted (ACTUAL)

August 8, 2018

Study Record Updates

Last Update Posted (ACTUAL)

November 15, 2018

Last Update Submitted That Met QC Criteria

November 14, 2018

Last Verified

November 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • MullKT

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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