Neuromusculoskeletal Alterations After ACL Injury (NCT07163468) | Clinical Trial Compass
CompletedNot Applicable
Neuromusculoskeletal Alterations After ACL Injury
Turkey (Türkiye)60 participantsStarted 2025-06-01
Plain-language summary
This study investigated how anterior cruciate ligament (ACL) injuries affect not only the knee joint but also brain activity, reaction speed, and psychological readiness to return to sports. A total of 60 male athletes, aged 18 to 30 years, were evaluated in three groups: healthy athletes, athletes who had undergone primary ACL reconstruction, and athletes who had undergone revision ACL reconstruction.
The study measured brain activity with electroencephalography (EEG), reaction time with a computer-based test, and psychological status with standardized questionnaires. The findings showed that athletes with revision ACL surgery had more difficulties in attention control, slower reaction times, and greater psychological barriers compared to the other groups.
These results suggest that ACL injuries and surgeries may influence not only physical recovery but also brain function and psychological readiness. The study highlights the importance of considering neuromuscular, cognitive, and emotional aspects when planning rehabilitation and return-to-sport decisions.
Who can participate
Age range
18 Years – 30 Years
Sex
MALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Male athletes
Age between 18 and 30 years
Regular participation in amateur or professional sports
Completion of ACL rehabilitation (for surgical groups) at least 6 months before enrollment
Ability to undergo EEG and reaction time testing
Provision of signed informed consent
Exclusion Criteria:
History of neurological or psychiatric conditions (e.g., epilepsy, ADHD, depression)
Additional lower extremity injuries or orthopedic surgeries
Metal implants or scalp conditions incompatible with EEG
Uncorrected visual or auditory deficits
Systemic illnesses (e.g., diabetes, multiple sclerosis, neuropathy)
Use of psychoactive medication
Any cognitive or physical limitation interfering with testing procedures
Female participants (to avoid hormonal confounding effects on EEG recordings)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Frontal EEG Theta/Beta Ratio
Timeframe: Single assessment on the study day (June-July 2025)