- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01933737
Kinesio Taping Effect on Postural Balance in Elderly
August 30, 2013 updated by: Paulo Roberto Veiga Quemelo, University of Franca
The elderly population has increased significantly in the last years.
The number of falls has also increased due to the decrease of balance.
The Kinesio Taping (KT) is a method with the aim to improve muscle physiology, proprioception, coordination and balance.
The aim of the study was to investigate the effect of KT on postural balance in the elderly.
We evaluated 62 elderly with a mean age of 67.98±5.321,
female, submitted to the protocol for the application of KT in gastrocnemius muscles of the midfoot and a placebo tape (3M Micropore) in the control group.
The application of the tapes was bilateral.
Half of the participants (n=31) received KT in the lower limbs, while the control group (n=31) was applied placebo tape.
To analysis of posture and balance, we used a force plate to record stabilometric signals.
Both groups were evaluated post-application and 48 hours after application of the tape.
The variables used were total displacement in centimeters (cm), amplitude AP (anterior-posterior) and ML (medial-lateral) in centimeters, area (cm²) and speed AP and ML in centimeters for seconds.
The experimental protocol was performed in standing posture and the subjects were instructed to stand with feet apart, eyes open to look at the fixed point 1.5 m from force plate in a horizontal direction.
It was requested that the elderly maintain the position for a time of 40 seconds to collect data The data were collected immediately post application of tapes and after 48 hours.
The data was tabulated, descriptive statistics were calculated.
Statistical analysis was performed using the GraphPad Prism 4.0 software (Prism, Chicago, IL).
The Kolmogorov Smirnov test was used to verify the data distribution.
Differences between the means were evaluated using the Student T test for the normally distributed data, and using the Mann-Whitney test for the data not normally distributed.
Significance levels were set at p<0.05.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Detailed Description
The Kinesio Taping Group (KTG) was composed of 31 participants that received the application of KT (K-Taping®) on the gastrocnemius muscle and the muscles of the midfoot.
The placebo tape group (PTG) was composed of 31 participants that received the application of a placebo tape (3M Micropore®) on the same muscles of both limbs.
The order of application of KT tape and placebo was conducted randomly among the elderly.
Before the tape applying the site was cleaned with 70% ethanol for better fixation of the tape and for both groups were determined the application technique in "I" shaped.
This technique consist in placing two tapes that format.
The first tape was placed along the length of the plantar aponeurosis fixed point in the middle third of the medial gastrocnemius muscle to the metatarsal phalangeal joint.
The second tape was also applied in "I" shaped without fixed point was placed around the midfoot arch in the direction of tension lines to assist with the metatarsal arch support.
Study Type
Interventional
Enrollment (Actual)
61
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
-
-
Sao Paulo
-
Franca, Sao Paulo, Brazil, 14404600
- University of Franca
-
-
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
60 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- elderly, gender female
Exclusion Criteria:
- No severe orthopedic diseases
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: Prevention
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Kinesio Taping Group
The Kinesio Taping group (KTG) (n = 31 elderly women) were submitted to the protocol of applying Kinesio Taping for gastrocnemius muscle and the muscles of the median foot.
The application of the tapes was bilateral limbs.
The subjects were evaluated post-application and 48 hours after application of the tape.
|
The Kinesio Taping group (KTG) (n = 31 elderly women) were submitted to the protocol of applying Kinesio Taping for gastrocnemius muscle and the muscles of the median foot.
The application of the tapes was bilateral limbs.
The subjects were evaluated post-application and 48 hours after application of the tape.
|
|
Experimental: Placebo tape group
The placebo tape group (PTG) (n = 31 elderly women) were submitted to the protocol of applying placebo tape (3M Micropore) for gastrocnemius muscle and the muscles of the median foot in the same way that KTG.
The application of the tapes was bilateral limbs.
The subjects were evaluated post-application and 48 hours after application of the tape.
|
The placebo tape group (PTG) (n = 31 elderly women) were submitted to the protocol of applying placebo tape (3M Micropore) for gastrocnemius muscle and the muscles of the median foot in the same way that KTG.
The application of the tapes was bilateral limbs.
The subjects were evaluated post-application and 48 hours after application of the tape.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Force plate to postural balance
Time Frame: 6 months
|
To analysis of posture and balance, we used a force plate to record stabilometric signals.
Both groups were evaluated post-application and 48 hours after application of the tape.
The variables used were total displacement in centimeters (cm), amplitude AP (anterior-posterior) and ML (medial-lateral) in centimeters, area (cm²) and speed AP and ML in centimeters for seconds.
We did not observe adverse effects
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Paulo RV Quemelo, PhD, University of Franca
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
January 1, 2012
Primary Completion (Actual)
January 1, 2012
Study Completion (Actual)
January 1, 2013
Study Registration Dates
First Submitted
August 21, 2013
First Submitted That Met QC Criteria
August 30, 2013
First Posted (Estimate)
September 2, 2013
Study Record Updates
Last Update Posted (Estimate)
September 2, 2013
Last Update Submitted That Met QC Criteria
August 30, 2013
Last Verified
August 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- UNIFRAN
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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