- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07650006
AI-Based Hamstring Injury Risk Analysis and Effects of the FUNBALL Program
June 10, 2026 updated by: Yeditepe University
AI-Based Hamstring Injury Risk Analysis and the Effects of the FUNBALL Program on Physical Performance and Cognitive Function in Professional Football Players
This study investigates hamstring injury risk in football players using artificial intelligence-based motion analysis (OpenPose) and evaluates the effects of a targeted exercise intervention (FUNBALL).
Hamstring risk is assessed during a 30-m sprint using sagittal-plane video analysis, and players classified as medium or high risk receive a four-month FUNBALL program.
A pre-post intervention design is employed, with sprint performance, agility, balance, jumping ability, kicking power, and cognitive function assessed using standardized field and cognitive tests.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Before the implementation of the FUNBALL program, artificial intelligence (OpenPose) based hamstring risk analysis and 30-meter sprint test, 505 agility and direction change test, modified star balance test, 5-point jump test, maximum shot distance test and cognition tests will be applied as pre-tests (18,19).
AI risk analysis will be done by examining video (30 frame rate) captured with a phone camera (iPhone 14 Pro) from the sagittal (side) plane during the 240 m sprint test.
The camera will be positioned 15 meters from the level of the middle of the 30-meter sprint test with the help of a tripod.
It will follow the participant's run for 30 meters in motion.
The football player will be asked to do a 30 m sprint with 3 repetitions and the average of 3 repetitions will be taken as a basis.
According to the artificial intelligence risk analysis, the FUNBALL program will be applied to medium and high risk groups for 4 months.
At the end of the Middle Program, the same parameters will be re-evaluated.
Hamstring risk analysis and speed parameter will be evaluated with 30 meter sprint test, agility parameter 505 with direction change and agility test, cognition parameter with color word stroop test, n-back test and digit span test, balance and proprioception parameter with modified star balance test, jump parameter with 5-point jump test, and power parameter with maximum shot distance test.
Study Type
Interventional
Enrollment (Actual)
30
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
-
-
Büyükçekmece
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Istanbul, Büyükçekmece, Turkey (Türkiye), 34537
- Istanbulspor Ömer Sarıalioglu Football Team Facilitu
-
-
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
Yes
Description
Inclusion Criteria:
- To be a professional football player between the ages of 18-35.
- Not having a history of ligament, joint, bone, muscle or tendon injury that requires at least 2 months away from the field in the last 6 months.
- Not having an active disability.
- To have verbal and written communication skills who accept to participate in the study voluntarily and to perform exercise applications.
Exclusion Criteria:
- Presence of an active disability
- Having a history of ligament, joint, bone, muscle or tendon injury that requires at least 2 months away from the field in the last 6 months.
- Vestibular or disconnected vision problems
- History of cancer
- Illiteracy
- Mental and cognitive disorders that may affect 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
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: FUNBALL Intervention Arm
|
The FUNBALL Prevention Program is an evidence-based injury prevention exercise program described in the literature.
The program was developed by Obertinca et al. and has been shown to reduce thigh muscle injury incidence by approximately 38% in football players.
In the present study, the FUNBALL program is implemented as a structured training intervention aimed at reducing hamstring injury risk.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Classified as High Hamstring Injury Risk by OpenPose-Based Biomechanical Analysis
Time Frame: Baseline (Day 0) and post-intervention (Week 12)
|
Outcome measure: Number of participants classified as high hamstring injury risk.
Assessment tool: OpenPose-based biomechanical motion analysis of a 30-meter sprint.
Classification is based on hip flexion angle, knee extension angle, and terminal swing phase mechanics.
Unit of measure: Number of participants classified as high risk.
|
Baseline (Day 0) and post-intervention (Week 12)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
505 COD Agility Test
Time Frame: Baseline (Day 0) and post-intervention (Week 12)
|
The 505 Change of Direction (COD) test is a widely used field-based assessment designed to evaluate an athlete's ability to decelerate, rapidly change direction, and re-accelerate over a short distance.
The players are going to sprint forward 10 m, perform a 180-degree turn off a designated foot at the 5-m mark, and sprint back as quickly as possible, with total time is going to record using electronic timing gates or a stopwatch.
|
Baseline (Day 0) and post-intervention (Week 12)
|
|
Number of Players With Elevated Hamstring Injury Risk During Sprint Testing
Time Frame: Baseline (Day 0) and post-intervention (Week 12)
|
The primary outcome will be the number of players identified with elevated hamstring injury risk during a 30-m sprint test, assessed using an artificial intelligence-based movement analysis.
|
Baseline (Day 0) and post-intervention (Week 12)
|
|
N-Back Task Accuracy (%)
Time Frame: Baseline (Day 0) and Post-Intervention (Week 12)
|
Working memory performance assessed using a computerized N-Back task and reported as percentage accuracy (%).
|
Baseline (Day 0) and Post-Intervention (Week 12)
|
|
Digit Span Total Score
Time Frame: Baseline (Day 0) and Post Intervention (Week 12)
|
Total number of correctly recalled digits during a computerized Digit Span task.
|
Baseline (Day 0) and Post Intervention (Week 12)
|
|
Composite Reach Distance in Modified Star Excursion Balance Test
Time Frame: Baseline ( Day 0) and Post-Intervention (Week 12)
|
Composite normalized reach distance during the Modified Star Excursion Balance Test.
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Baseline ( Day 0) and Post-Intervention (Week 12)
|
|
Horizontal Distance in Multiple Five Bounds Test
Time Frame: Baseline (Day 0) and Post-Intervention (Week 12)
|
Horizontal distance achieved during the Multiple Five Bounds Test assessing horizontal power.
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Baseline (Day 0) and Post-Intervention (Week 12)
|
|
Maximal Soccer Ball Kicking Distance
Time Frame: Baseline (Day 0) and Post-Intervention (Week 12)
|
Maximum horizontal distance of a soccer ball following a maximal instep kick.
|
Baseline (Day 0) and Post-Intervention (Week 12)
|
|
Stroop Reaction Time
Time Frame: Baseline (Day 0) and Week 12
|
Mean reaction time during incongruent trials of a computerized Stroop task.
|
Baseline (Day 0) and Week 12
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Elif Tuğçe t Çil Sertöz, Asst. Prof. Dr., Yeditepe University
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)
February 1, 2026
Primary Completion (Actual)
April 25, 2026
Study Completion (Actual)
April 25, 2026
Study Registration Dates
First Submitted
December 29, 2025
First Submitted That Met QC Criteria
June 10, 2026
First Posted (Actual)
June 16, 2026
Study Record Updates
Last Update Posted (Actual)
June 16, 2026
Last Update Submitted That Met QC Criteria
June 10, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Yeditepe U1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Time Frame
January 2026-January 2027
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
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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