Investigation of the Effect of Foam Roller and Kinesiotape Application on Performance Parameters, Pain and Fatigue With Football Players

November 21, 2021 updated by: Muhammet Alper Karabag, Pamukkale University

Investigation of the Effect of Foam Roller and Kinesiotape Application on Performance Parameters, Pain and Fatigue

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.

Study Overview

Status

Enrolling by invitation

Conditions

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

Interventional

Enrollment (Anticipated)

18

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

    • Efeler
      • Aydin, Efeler, Turkey, 09100
        • Aydın Adnan Menderes 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 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

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

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: 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
The investigators use Foam roller to 3 muscle groups per leg then conduct a dynamic warm up program and conduct performance tests
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.
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

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
Fatigue
Time Frame: immediately after application
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
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
in 1 hour after application
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
Dynamic reaction time
Time Frame: in 1 hour after application
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
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.
in 1 hour after application

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Anticipated)

November 21, 2021

Primary Completion (Anticipated)

July 15, 2022

Study Completion (Anticipated)

July 15, 2022

Study Registration Dates

First Submitted

October 28, 2021

First Submitted That Met QC Criteria

November 21, 2021

First Posted (Actual)

November 23, 2021

Study Record Updates

Last Update Posted (Actual)

November 23, 2021

Last Update Submitted That Met QC Criteria

November 21, 2021

Last Verified

November 1, 2021

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)?

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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