- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02431910
Immediate and Delayed Effects of Kinesio Taping on the Neuromuscular Performance (IDEKTNP)
April 24, 2017 updated by: Jamilson Simões Brasileiro, Universidade Federal do Rio Grande do Norte
Immediate and Delayed Effects of Kinesio Taping on the Neuromuscular Performance, Balance and Lower Limb Function of Healthy Subjects: Randomized Clinical Trial
The purpose of this study is analyze the immediate and late effects of the application of KT in neuromuscular performance of the quadriceps in postural balance and function of the lower limb of healthy subjects.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Sixty volunteers, females will be recruited and randomly divided into 3 groups with 20 members each: control group (CG) - 10 minutes at rest; placebo group (PG) - Kinesio Taping (KT) without application of tension in the vastus lateralis (VL), vastus (VM) and rectus femoris (RF); and Kinesio Taping group (KTG) - application of KT with tension in VL, VM and RF.
All volunteers will be evaluated for their distance from the single and triple hop test, postural balance (baropodometry), the joint position sense (JPS), the knee extensor torque (concentric and eccentric assessment at 60 °/s) and electromyographic activity of the VL muscle in five distinct stages: the first before the intervention (AV1), the second immediately after (AV2) and the following three 24h (AV3), 48 (AV4) after the intervention protocol.
Soon after the AV4, KT will be removed after 24 hours and take place the last review (AV5).
Study Type
Interventional
Enrollment (Actual)
60
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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Rio Grande do Norte
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Natal, Rio Grande do Norte, Brazil, 59078-970
- Universidade Federal do Rio Grande do Norte
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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 28 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Be recreationally active, with no history of osteomyoarticular lesion or surgery in the lower limbs in the previous six months, non-corrected neurological, vestibular, visual and/or hearing impairments, in addition to displaying no allergy to adhesive material.
Exclusion Criteria:
- Individuals experiencing pain during collection procedures or who do not perform exercises as instructed by the researchers would be excluded.
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: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control group
The control group remains at rest for 10 minutes, which is not applied KT in the RF, VL and VM muscles.
The volunteers of this group perform all evaluation without the application of KT
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Placebo Comparator: Placebo group
The Kinesio Taping (KT) is applied on the vastus lateralis (VL), vastus medialis (VM) and rectus femoris (RF) muscles longitudinally from proximal to the distal.
For the RF proximal anchor is applied 5cm below the anterior superior iliac spine and the distal anchor the upper edge of the patella.
VL in the proximal and distal anchor will be fixed in greater trochanter of the femur and the lateral edge of the patella.
As for the VM muscle proximal anchor will be applied to the middle third from the medial region of the thigh and the distal anchor on the medial edge of the patella.
The anchors are applied with 0% tension and therapy area will follow on the belly of the muscles with a 0%.
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application of KT without tension in the vastos medialis, rectus femoris and vastus lateralis muscles
Other Names:
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Experimental: Kinesio Taping group
The Kinesio Taping (KT) is applied on the vastus lateralis (VL), vastus medialis (VM) and rectus femoris (RF) muscles longitudinally from proximal to the distal.
For the RF proximal anchor is applied 5cm below the anterior superior iliac spine and the distal anchor the upper edge of the patella.
VL in the proximal and distal anchor will be fixed in greater trochanter of the femur and the lateral edge of the patella.
As for the VM muscle proximal anchor will be applied to the middle third from the medial region of the thigh and the distal anchor on the medial edge of the patella.
The anchors are applied with 0% tension and therapy area will follow on the belly of the muscles with a 50%.
This application will be held with subjects standing on one foot, with the hip of the non-dominant limb at 0º and knee flexed at 90º.
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application of KT with tension in the vastos medialis, rectus femoris and vastus lateralis muscles
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle Performance measured through isokinetic dynamometry
Time Frame: baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Change from baseline in muscle performance at 72 hours.Immediate and Delayed Effects of Kinesio Taping in the muscle performance will be measured through isokinetic dynamometry and the variables analyzed will be peak torque normalized for body weight, mean power, total work and time to peak torque.
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baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Balance measured through baropodometry
Time Frame: baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Change from baseline in balance at 72 hours.
Immediate and Delayed Effects of Kinesio Taping in balance will be Measured by baropodometry
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baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Lower limb function
Time Frame: baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Change from baseline in lower limb function at 72 hours.
Immediate and Delayed Effects of Kinesio Taping will be measure through distance of the single and triple hop test.
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baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Proprioception measured through joint position sense in the isokinetic dynamometer
Time Frame: baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Change from baseline in proprioception at 72 hours.
Immediate and Delayed Effects of Kinesio Taping in the proprioception will be measured through joint position sense
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baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Muscle activation measured through surface electromyography
Time Frame: baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Change from baseline in muscle activation at 72 hours.
Immediate and Delayed Effects of Kinesio Taping in Muscle activation will be Measured by surface electromyography
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baseline, one minute after the intervention protocol, 24 hours, 48 hours and 72 hours after the intervention protocol.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jamilson S Brasileiro, PhD, Universidade Federal do Rio Grande do Norte
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)
June 1, 2015
Primary Completion (Actual)
December 1, 2015
Study Completion (Actual)
December 1, 2015
Study Registration Dates
First Submitted
April 9, 2015
First Submitted That Met QC Criteria
April 27, 2015
First Posted (Estimate)
May 1, 2015
Study Record Updates
Last Update Posted (Actual)
April 25, 2017
Last Update Submitted That Met QC Criteria
April 24, 2017
Last Verified
April 1, 2017
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 752.302
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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