Clinical Trials Logo

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05130502
Other study ID # MAKarabag
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date November 21, 2021
Est. completion date July 15, 2022

Study information

Verified date November 2021
Source Pamukkale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 18
Est. completion date July 15, 2022
Est. primary completion date July 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Playing in Aydin 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 Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Turkey Aydin Adnan Menderes University Aydin Efeler

Sponsors (2)

Lead Sponsor Collaborator
Pamukkale University Aydin Adnan Menderes University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle Pain 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
Primary Fatigue 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
Primary Sprint 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
Primary Agility 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
Primary Dynamic reaction time 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
Primary Flexibility 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
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05559255 - Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI N/A
Terminated NCT04356352 - Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain Phase 2/Phase 3
Completed NCT04748367 - Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care N/A
Completed NCT05057988 - Virtual Empowered Relief for Chronic Pain N/A
Completed NCT04466111 - Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
Recruiting NCT05868122 - A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy Phase 3
Recruiting NCT06206252 - Can Medical Cannabis Affect Opioid Use?
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Enrolling by invitation NCT06087432 - Is PNF Application Effective on Temporomandibular Dysfunction N/A
Completed NCT05508594 - Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 Phase 2/Phase 3
Recruiting NCT03646955 - Partial Breast Versus no Irradiation for Women With Early Breast Cancer N/A
Active, not recruiting NCT03472300 - Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
Completed NCT03678168 - A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries N/A
Completed NCT03931772 - Online Automated Self-Hypnosis Program N/A
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Completed NCT02913027 - Can We Improve the Comfort of Pelvic Exams? N/A
Terminated NCT02181387 - Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor? Phase 4
Recruiting NCT06032559 - Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment Phase 3
Active, not recruiting NCT03613155 - Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care