Trial · NCT07650006
AI-Based Hamstring Injury Risk Analysis and Effects of the FUNBALL Program
NCT07650006, Not applicable, Completed, Yeditepe University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. AI-Based Hamstring Injury Risk Analysis and Effects of the FUNBALL Program. Trials, record NCT07650006. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07650006
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- AI-Based Hamstring Injury Risk Analysis and Effects of the FUNBALL Program
- NCT number
- NCT07650006
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 30 participants, actual
- Lead sponsor
- Yeditepe University
- Conditions
- Healthy, Healthy Adult Male
- Interventions
- FUNBALL Prevention Program
- First posted
- 2026-06-16
- Last updated
- 2026-06-16
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants Classified as High Hamstring Injury Risk by OpenPose-Based Biomechanical Analysis | 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. |
| Secondary | 505 COD Agility Test | 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. |
| Secondary | Number of Players With Elevated Hamstring Injury Risk During Sprint Testing | 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. |
| Secondary | N-Back Task Accuracy (%) | Baseline (Day 0) and Post-Intervention (Week 12) | Working memory performance assessed using a computerized N-Back task and reported as percentage accuracy (%). |
| Secondary | Digit Span Total Score | Baseline (Day 0) and Post Intervention (Week 12) | Total number of correctly recalled digits during a computerized Digit Span task. |
| Secondary | Composite Reach Distance in Modified Star Excursion Balance Test | Baseline ( Day 0) and Post-Intervention (Week 12) | Composite normalized reach distance during the Modified Star Excursion Balance Test. |
| Secondary | Horizontal Distance in Multiple Five Bounds Test | Baseline (Day 0) and Post-Intervention (Week 12) | Horizontal distance achieved during the Multiple Five Bounds Test assessing horizontal power. |
| Secondary | Maximal Soccer Ball Kicking Distance | Baseline (Day 0) and Post-Intervention (Week 12) | Maximum horizontal distance of a soccer ball following a maximal instep kick. |
| Secondary | Stroop Reaction Time | Baseline (Day 0) and Week 12 | Mean reaction time during incongruent trials of a computerized Stroop task. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests4
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| 1-Back Task | Secondary outcome | ConductCognition |
| 2-Back Task | Secondary outcome | ConductCognition |
| Digit Span Test | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07650006
GET https://conductscience.org/api/trials/v1/NCT07650006/registered