The Effect of Exercise on Amateur American Football Players

November 4, 2024 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

Completed

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 (Actual)

43

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

  • Turkey
    • None Selected
      • Istanbul, None Selected, Turkey, 34353
        • Hazal GENÇ

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 withVideo-Based
Other: Exercise with Video-Based
A program of stability and balance exercises will be provided
Active Comparator: Standart Exercise-Home-Based
Other: Standart exercise-Home-Based
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.

Sponsor

Istanbul Medipol University Hospital

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.

General Publications

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 (Actual)

June 17, 2023

Study Completion (Actual)

August 17, 2024

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 (Estimated)

November 5, 2024

Last Update Submitted That Met QC Criteria

November 4, 2024

Last Verified

November 1, 2024

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

product manufactured in and exported from the U.S.

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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