- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05130502
Investigation of the Effect of Foam Roller and Kinesiotape Application on Performance Parameters, Pain and Fatigue With Football Players
Investigation of the Effect of Foam Roller and Kinesiotape Application on Performance Parameters, Pain and Fatigue
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The aim of our study is to compare the effects of foam roller plus dynamic stretching and kinesiotape plus dynamic stretching on performance parameters,pain and fatigue in football players. The results of our study will show the effects of the best choice between applications and help to reduce waste of time. Performance parameters include; flexibility, dynamic reaction time, sprint and agility.
The hypotheses the investigators will test for this purpose; H1: Foam Roller application is more effective on performance parameters than Kinesiotape application. H2: Foam Roller application is more effective on pain than Kinesiotape application. H3: Foam Roller application is more effective on fatigue than Kinesiotape application.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Efeler
-
Aydin, Efeler, Turkey, 09100
- Aydın Adnan Menderes University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Playing in Aydın Adnan Menderes University Football Team and volunteering.
Exclusion Criteria:
- Individuals with medical conditions that may affect their ability to complete the work, such as recurrent muscle, bone, tendon, and ligament injuries, or a history of prior lower extremity surgery.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Foam roller
Individuals perform Foam roller on bilateral legs and the muscles include Quadriceps, hamstring and gastrocnemius and soleus with a dynamic warm up program The investigators conduct the test for 2 sets and 60 seconds with 30 seconds rest period per muscle
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The investigators use Foam roller to 3 muscle groups per leg then conduct a dynamic warm up program and conduct performance tests
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Active Comparator: Kinesiotape
Individuals perform Kinesiotape on bilateral legs and the muscles include Quadriceps, hamstring and gastrocnemius and soleus with a dynamic warm up program The investigators conduct the kinesiotape per muscle and will wait for 45 minutes for bring out the effects.
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The investigators use Kinesiotape to 3 muscle groups per leg, wait 45 minutes for bring out the effects then conduct a dynamic warm up program and conduct performance tests
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle Pain
Time Frame: immediately after application
|
With VAS scale ; The scale goes from '0' to '10' points.
A score of 0 means 'I have no pain' and a score of 10 means 'I have very severe pain'.
|
immediately after application
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Fatigue
Time Frame: immediately after application
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With BORG scale; The scale goes from '0' to '10' points.
0 points means 'I am not tired at all' and 10 points means 'I have very severe fatigue'.
|
immediately after application
|
Sprint
Time Frame: in 1 hour after application
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20m sprint test; 20-meter sprint test will be applied in the study.
Participants will be positioned with one foot in front of the other and not crossing the starting line.
Swinging movements to the right-left or forward-backward will not be allowed before the run.
Participants will run a single max sprint at 20 meters and sprint time will be recorded using an automatic light switch system (SMARTSPEED™, Fusion Sport Inc., Australia; 1000 Hz).
A single measurement will be taken from subjects
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in 1 hour after application
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Agility
Time Frame: in 1 hour after application
|
The 18.3 m pro-agility (505) test will be applied.
The test will start from 3 pontoons that are 4.6 meters from each other, over the middle pontoon.
The individual will run 4.6 m to the pontoon on the left first.
After his foot contacts the line (followed by the line judge), he will turn around and run up to the pontoon located 9.1 m to the right (4.6 m to the right of the center line) and again to touch the line with his foot.
After making contact with the right line, it will turn and run towards the center pontoon.
The best time of two attempts will be recorded as agility speed.
Participants will rest for 1 minute between trials.
All measurements will be performed using (Fusionsports Smartspeed™ PRO photocell, Fusion Sport, Queensland, Australia).
|
in 1 hour after application
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Dynamic reaction time
Time Frame: in 1 hour after application
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Dynamic reaction time (DRT) will be evaluated using the Blazepod system, which includes "pods" equipped with touch sensors and LED lights.
Three of the blazepod pods will be affixed to a wall 1.5 m above the floor, each 1.5 m apart.
During testing, when a random single bin is lit, the subject will be instructed to react as quickly as possible by running towards the light and touching the bin.
Subjects will do so with a total of 6 randomized light triggers for a single trial.
Subjects will perform 2 trials with 3 minutes rest.
Average reaction time will be calculated for each trial and the best score will be used for analysis.
|
in 1 hour after application
|
Flexibility
Time Frame: in 1 hour after application
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The investigators use 'Hudl' tecnique.
Hip and knee flexion measurements will be calculated with digital goniometer in supine (for hip) and prone (for knee) positions.
3 trial will be taken and will be averaged.
With the Hudl technique, the necessary angles will be measured with the help of the smartphone.
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in 1 hour after application
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MAKarabag
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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