- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01792908
Kinesio Tape Effects on Ankle Proprioception
February 14, 2013 updated by: Iris Miralles Rull, University Rovira i Virgili
Has Kinesio Tape Effects on Ankle Proprioception? A Randomized Clinical Trial
The aim of the present study was to establish whether Kinesio Tape (KT) on the ankle (Kase protocol for the lateral ankle ligament) improves Joint Position Sense (JPS) in healthy volunteers immediately after its application and 48 hours later.
Study Overview
Detailed Description
The investigators assessed Joint Position Sense (JPS) through the difference of error (DoE) and the deviation of the target angle (DTA).
JPS was assessed before the Kinesio Tape (KT) was placed, immediately after and 48 hours later.
Study Type
Interventional
Enrollment (Actual)
73
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
-
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Tarragona
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Reus, Tarragona, Spain, 43201
- Faculty of Medicina i Ciències de la Salut; University Rovira i Virgili.
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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
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Must be signed the informed consent
- Aged between 18 and 35 years
- Did not suffered from ankle or foot skin diseases
- Active dorsal/plantarflexion ARoM equal to or above 15º and inversion/eversion
- ARoM equal to or above 5º.
Exclusion Criteria:
- Traumatic, neurological or circulatory diseases diagnosed
- Joint laxity
- More than three ankle sprains in their lives or one in the last 12 months that required treatment and ankle or foot pain at the time of study enrolment in the non-dominant lower limb.
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: KT group
The KT group received ankle KT on the lateral ligament in the non-dominant leg and a recommendation guide.
The Kinesio tape procedure was carried out by the same certified athletic therapist to ensure consistency throughout the study.
|
The KT used was Kinesiology Tape® of 5 cm and it was applied according to Kase protocol (Kase K).
The first layer of tape consisted of a single strip placed over the anterior talofibular ligament from insertion to origin, with a 50% tension, except the two-centimetre proximal and distal ends, applied with no tension.
The same procedure was repeated for the calcaneofibular ligament and posterior talofibular ligament
Other Names:
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No Intervention: Control group
Any intervention has been applied.
Using another kind of tape or a different KT application for control group may increase cutaneous information, undermining our goal.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Joint position sense on the Difference of Error from the target angle
Time Frame: Change from baseline in proprioception at 48h
|
The primary outcome, difference of error (DE) in degrees was calculated to show changes in error from the target angle over time.
We compared error, before and immediately after intervention (DoE 1-2), before and 48 hours after intervention (DE 1-3) and immediately and 48 hours after intervention (DE 2-3).
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Change from baseline in proprioception at 48h
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Deviation of the target angle
Time Frame: Change from baseline in proprioception at 48h
|
We also calculated the deviation from the target angle (DTA) in degrees, this secondary outcome to describe the direction of error when subjects tried to reproduce the requested position.
Deviation was obtained encoding net error taking as correct position when the target and the estimated angle were equal, considering the precision of the electronic plate a valid range (0.4 degrees).
Values above this range were classified as Overestimation and as Underestimation when values were below this range.
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Change from baseline in proprioception at 48h
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Iris Miralles, University Rovira i Virgili
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.
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
October 1, 2011
Primary Completion (Actual)
April 1, 2012
Study Completion (Actual)
April 1, 2012
Study Registration Dates
First Submitted
February 12, 2013
First Submitted That Met QC Criteria
February 14, 2013
First Posted (Estimate)
February 15, 2013
Study Record Updates
Last Update Posted (Estimate)
February 15, 2013
Last Update Submitted That Met QC Criteria
February 14, 2013
Last Verified
February 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- T11230S
- R02/2010 (Other Grant/Funding Number: Col.legi de Fisioterapeutes de Catalunya)
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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