- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03619629
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
Status
Completed
Conditions
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.
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)
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
Keywords
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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