Effect of Neck Training on Outcomes Related to Sport-Related Concussion (NCT06774976) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Neck Training on Outcomes Related to Sport-Related Concussion
Sweden50 participantsStarted 2025-09
Plain-language summary
Sport-related concussion (SRC) is a significant concern in soccer. This pilot quasi-experimental trial aims to investigate the efficacy and acceptability of an evidence-based neck resistance exercise program in female soccer athletes for SRC prevention. The 8-week intervention includes dynamic and static neck exercises designed to reduce linear and rotational head accelerations, improve neck muscle strength, and minimise SRC risk. The study will evaluate program outcomes through laboratory testing, questionnaires, and user feedback. Findings from this pilot study will inform the design and implementation of a full-scale study, aiming to advance preventive strategies in SRC and address the underrepresentation of female athletes in research.
Who can participate
Age range
16 Years
Sex
FEMALE
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:
* Teams that are located in Skåne county
* Teams that are trained by professional trainers who are financially compensated for their work
* Teams that are not engaged in any targeted neck-strengthening exercises during the trial period beyond those prescribed within the trial
* Players that are 16 years of age or older
* Players that regularly attend all senior-level team activities, including training and match sessions
* Players that free of any injuries to their upper or lower limbs, torso, neck, or head at the time of enrolment
* Players with no history of undiagnosed neck pain within the previous three months.
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
Linear head acceleration
Timeframe: Measurements will be taken at baseline and after the 8-week intervention program.
2
Rotational head acceleration
Timeframe: Measurements will be taken at baseline and after the 8-week intervention program.
3
Isometric neck strength
Timeframe: Measurements will be taken at baseline and after the 8-week intervention program.