- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07726459
Comparison of Foot Reaction Time, Body Awareness, Balance, and Core Stabilization Performance in Young Amateur Football Players From Different Age Groups
July 22, 2026 updated by: Ezgi Türkmen, Health Institutes of Turkey
Aim of the study is to compare foot reaction time, body awareness, balance, and core stabilization performance in 50 amateur football players aged 13-19 (Group I: 13-15 years, and Group II: 16-19 years) according to age, and to determine age-related performance differences.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
The aim of this study is to evaluate foot reaction time, body awareness, balance, and core stabilization performance in amateur football players aged 13-19 years, to examine how these parameters change according to age groups, and to compare and reveal developmental differences in these performance components in young athletes.
This research study is designed as an observational and cross-sectional evaluation study.
The study aims to collect and compare the data according to age on participants' sociodemographic data, reaction time using the Nelson Foot Reaction Test, awareness levels using the Body Awareness Questionnaire, balance status using the Y-Balance Test, and endurance levels using the McGill Core Endurance Test.
Study Type
Observational
Enrollment (Estimated)
50
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Amateur Football Players Aged 13-19
Description
Inclusion Criteria:
- Being a licensed amateur football player aged 13-19.
- Having played football regularly (at least 3 days a week) for the past year.
- Voluntarily agreeing to participate in the study.
Exclusion Criteria:
- Having a diagnosis of any neurological, orthopedic, or systemic disorder.
- Having a diagnosis of visual impairment or any systemic disease affecting balance.
- Having any significant physical limitations that would prevent the administration of the tests.
- Having a diagnosed psychological disorder that would hinder communication.
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
Cohorts and Interventions
Group / Cohort |
|---|
|
Group I
Amateur Football Players Aged 13-15
|
|
Group II
Amateur Football Players Aged 16-19
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nelson Foot Reaction Test
Time Frame: Baseline
|
The Nelson Foot Reaction Test measures simple foot-eye reaction time and lower limb neuromuscular coordination.
Using a drop ruler, it requires the subject to quickly stop or "trap" a falling measurement stick between their foot and a wall or the floor in response to an auditory or visual trigger.
The Reaction: The subject reacts as quickly as possible, pressing their foot forward to pinch/stop the falling ruler against the wall.Recording: The point where the ruler is stopped indicates the distance it traveled.
The reaction time is calculated using the formula: Reaction Time (seconds) = √2 * Distance (cm)/980.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Awareness Questionnaire (BAQ)
Time Frame: Baseline
|
BAQ is an 18-item self-report scale designed to measure how attentive you are to normal, non-emotional internal bodily processes.
It evaluates your sensitivity to everyday bodily cycles (like sleep and hunger), ability to detect subtle changes, and capacity to anticipate physical reactions.
Typically takes about 3 to 5 minutes.
Items are generally rated on a 1 to 7 scale, with higher total scores indicating greater perceived confidence and accuracy in monitoring your physical state over time.
|
Baseline
|
|
Y Balance Test (YBT)
Time Frame: Baseline
|
The YBT requires the athlete to balance on one leg whilst simultaneously reaching as far as possible with the other leg in three separate directions: anterior, posterolateral, and posteromedial.
Therefore, this test measures the athlete's strength, stability and balance in various directions.
The YBT composite score is calculated by summing the three reach directions and normalising the results to the lower limb length.
|
Baseline
|
|
McGill Core Endurance Test
Time Frame: Baseline
|
This test measures the stabilization capacity and muscle endurance of the core muscles (abdominal, back, oblique, and lower back muscles).
It is performed in four positions: Trunk Flexor Test, Trunk Extensor Test (Sorensen Test), Side Bridge Test (Left & Right).
The time (in seconds) spent maintaining the required positions is measured and recorded using a stopwatch.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
July 1, 2026
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Study Registration Dates
First Submitted
July 17, 2026
First Submitted That Met QC Criteria
July 22, 2026
First Posted (Actual)
July 24, 2026
Study Record Updates
Last Update Posted (Actual)
July 24, 2026
Last Update Submitted That Met QC Criteria
July 22, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- ETurkmen0126
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.