Cerebral and Cognitive Effects in Female Pro Soccer Players After Repeated Small Head Impacts
Official title: Cerebral and Cognitive Modifications in Retired Female Professional Soccer Players as Compared to Non Exposed to Repeated Cranial Impacts Sportswomen : Transverse Analytic Study
Run by University Hospital, Strasbourg, France · NCT06788262 · Data updated 2026-11-12
This study tests whether repeated minor head injuries in female pro soccer players are linked to brain changes and early cognitive differences after they retire.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 32 Years to 65 Years |
| Sex | Women only |
| Enrollment | 80 (estimated) |
| Sponsor | University Hospital, Strasbourg, France Academic / other |
| Locations | 1 site (Strasbourg) |
| Status | Recruiting |
| Started | September 13, 2025 |
| Main results expected | June 15, 2027 |
| Study ends | June 15, 2027 |
| Registry record updated | August 20, 2026 |
| Trial ID | NCT06788262 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women professional soccer players in France at the end of their careers (or retired within ~10 years) who have experienced repeated mild head injuries, plus age-matched controls with no head-injury exposure.
✕Probably not a fit
Individuals without exposure to repeated head injuries or with no brain MRI abnormalities may not benefit directly from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study uses MRI to examine brain structure and function in female professional soccer players who are at the end of their careers or have retired within about 10 years, comparing them with age-matched controls with little to no head-injury exposure. It focuses on diffusion, perfusion, functional MRI, brain volumes, cortical thickness, spectroscopy, and susceptibility imaging to detect microstructural and functional changes. The goal is to see if repeated mild head impacts are associated with MRI-detectable abnormalities and potential cognitive changes. Participants include exposed players and unexposed controls, with rigorous exclusion of prior severe head injuries. No treatment is being tested; the study is observational and analytic in nature.
Why it matters
Potential benefit: If successful, findings could help identify MRI markers of brain changes related to repeated head impacts in women and inform prevention and monitoring strategies.
How similar studies have gone: Prior work in concussion and diffusion/perfusion MRI has shown detectable brain changes after head injuries, though studies focusing on female soccer players are less common.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Exposed high-level athletes: female professional soccer players at the end of their career (32- years old) playing in France Ligue 1 or 2 exposed to repeated mild head injuries with no history of severe head injury or cerebral * Female High-level athletes not exposed to repeated mild head injuries: control group paired for age with female professional soccer players, who have never regularly participated in sports exposing them to head injuries (notably rugby, basketball, handball, American football, hockey, combat sports, etc.) and who have no history of head injury, even mild. Female Professional tennis players or former players will be preferentially recruited. Exclusion Criteria: * Refusal to be informed of abnormalities on MRI * Incapacity to give informed consent or under a legal protection order; * History of cerebral concussion including the presence after head shock of one or more of the following signs or symptoms: a period of confusion or disorientation, a period of loss of consciousness of 30 minutes or less, post-traumatic amnesia not exceeding 24 hours * History of severe head/brain injury; * History of neurological or psychiatric disorder; * Known cerebral abnormality diagnosed by an imaging exam (CT or MRI); * History or regular or occasional consumption of drugs, unweaned active smoking or weaned for less than 1 year, excessive consumption of alcohol (\> 20 g alcohol per day, evaluated with the formula "degree of alcohol × volume in cl × 8/1000"), weaned or not. * Usage of medication targeting the central nervous system in the 2 weeks preceding inclusion in the study; * Prior history of severe hypertension, diabetes, chronic heart disease, progressive or disabling disease; * Contraindication to MRI (claustrophobia, implanted material not compatible with MRI, refusal to be informed of abnormality discovered on MRI)
Where it's running
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Hôpitaux Universitaires de Strasbourg
Strasbourg, France Recruiting
Study contacts
- Principal investigator: Stéphane KREMER, MD — Hopitaux Universitaires de Strasbourg
- Study coordinator: Stéphane KREMER, MD
- Email: stephane.kremer@chru-strasbourg.fr
- Phone: 03 88 12 78 48
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.