Changes of Various Structures After Lisfranc Injury Compared to Healthy Individuals. (NCT06420856) | Clinical Trial Compass
CompletedNot Applicable
Changes of Various Structures After Lisfranc Injury Compared to Healthy Individuals.
Turkey (Türkiye)23 participantsStarted 2024-01-02
Plain-language summary
The effect of muscular strength deficits on postural control after Lisfranc injury has been explained in relation to stance duration and strength. However, the relationship between protective sole sensation and changes in ankle proprioception, balance, ankle mobility and Achilles tendon structural properties has been shown in previous studies. The aim of our study was to determine the possible changes in protective sole sensation, ankle proprioception, balance and functional capacity after Lisfranc injury and to analyse the relationship between these variables.
Who can participate
Age range
18 Years
Sex
ALL
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 for Lisfranc Injury Group:
* Having had a Lisfranc injury
* Having only one extremity injured
* Having received surgical treatment
* Being over 18 years old
Exclusion Criteria for Lisfranc Injury Group :
* Having a neurological problem,
* diabetes
* smoking
* untreated Lisfranc injury
* incomplete medical record
* not wanting to participate in the study
* having a neurovascular injury
Inclusion Criteria for Healthy Volunteer Group
* Being healthy
* Any foot pain, history of fractures, etc. Absence of circumstances
* Being over 18 years of age
Exclusion Criteria for Healthy Volunteer Group
* Not being healthy
* Any foot pain, history of fractures, etc.
* Not being over 18 years of age
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
Difference in plantar sensation in people with Lisfranc injuries compared to healthy people