- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05868655
The Effect of Exercise on Amateur American Football Players
May 19, 2023 updated by: hazal genc, Istanbul Medipol University Hospital
Football is a team activity that calls for numerous sophisticated talents, including speed, endurance, speed, strength, and quickness.
It is getting more and more popular among professional and amateur players, particularly in America.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Current research demonstrates that characteristics of American football players like body composition, sprint performance, metabolism, and strength are influenced by elements like the league played, training history, and position played.
The ability to generate power with both the upper and lower bodies, change direction quickly, accelerate quickly in both positive and negative directions, run quickly, engage in high-intensity collisions repeatedly, and maintain muscular strength endurance are all skills that players on the court may need.
Study Type
Interventional
Enrollment (Anticipated)
52
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 Contact
- Name: Hazal GENÇ
- Phone Number: 05413204291
- Email: hazaloksuz@gmail.com
Study Locations
-
-
None Selected
-
Istanbul, None Selected, Turkey, 34353
- Recruiting
- HAZAL genç
-
Contact:
- Hazal GENÇ
- Phone Number: 05413204291
- Email: hazaloksuz@gmail.com
-
Sub-Investigator:
- İREM SENA ERKEN
-
-
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
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Male individuals between the ages of 18-25
- Being an American football player
- Regular attendance at training sessions
Exclusion Criteria:
- Known neurological disorder
- Serious orthopedic disorders that will prevent him from exercising
- cognitive impairment
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Exercise with supervisor
|
A program of stability and balance exercises will be provided.
Participants will be asked to take the final measurements after the exercises have been monitored by a physical therapist for eight weeks.
|
Active Comparator: Standart Exercise
|
Participants will be asked to take the final measurements after the exercises have been monitored by a physical therapist for eight weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Tampa Kinesiophobia Scale
Time Frame: 8 weeks
|
The Tampa Kinesiophobia Scale is one of two scales that assesses pain-related fear.
This scale, which is frequently used in the literature, is based on avoidance due to fear, fear in work-related activities, fear of movement or re-injury.
The Tampa Scale for Kinesiophobia is a 17-item questionnaire that quantifies fear of movement.The original 17-item version of the scale creates scores ranging between 17 and 68 with higher scores indicating more fear of movement
|
8 weeks
|
Optojump
Time Frame: 8 weeks
|
The system can be activated with 2 cameras and at least 2 Optojump bars.
In the measurements, the vertical jump height was recorded with the optoJump system and the software of this system (Microgate, Bolzano, Italy).
The measurement of the vertical jump distance in centimeters is done by means of two bars in the OptoJump system with sensors that detect movement.
|
8 weeks
|
The duration of the jump (milliseconds) .(Optojump)
Time Frame: 8 weeks
|
The system can be activated with 2 cameras and at least 2 Optojump bars.
The duration of the jump (milliseconds).
|
8 weeks
|
The Biodex balance system
Time Frame: six weeks
|
The Biodex balance system (BDS) is one of the mechanical platforms frequently used in balance measurements.
It assesses balance through a platform that oscillates in the anteroposterior, mediolateral and general directions simultaneously.
|
six weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sit-Reach Test
Time Frame: 8 weeks
|
The classical sit-reach test will be used to assess flexibility.
According to meta-analyses, the classical sit-reach test is the most reliable method to evaluate hamstring flexibility.
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
April 17, 2023
Primary Completion (Anticipated)
June 17, 2023
Study Completion (Anticipated)
August 17, 2023
Study Registration Dates
First Submitted
April 17, 2023
First Submitted That Met QC Criteria
May 19, 2023
First Posted (Actual)
May 22, 2023
Study Record Updates
Last Update Posted (Actual)
May 22, 2023
Last Update Submitted That Met QC Criteria
May 19, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- American Football Players
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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