- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06715618
The Use of the Functional Movement Screen™ in Preventing Injuries in Amateur Rugby Players (FMSrugbyAMA)
The Use of the Functional Movement Screen™ in Preventing Injuries in Amateur Rugby Players: A Longitudinal Prospective Study
Rugby is a team contact sport that demands unparalleled physical engagement. This practice, which combines random running patterns with changes in speed and direction, also involves frequent contact situations with other players. These phases of the game account for 48% to 80% of total injuries. Injury prevention is an integral part of the physical therapist's expertise and plays a crucial role in reducing the occurrence of musculoskeletal injuries and mitigating their devastating consequences.
The implementation of a risk prevention tool is particularly relevant for a population prone to injuries. However, the practicality of such a tool must be considered, as adherence to an injury prevention program depends on the "perceived usefulness, intensity, and time investment of the program".
One tool appears to meet these criteria: the Functional Movement Screen™ (FMS™). This tool is designed to "evaluate an individual's functional movement patterns" and, according to its authors, can serve as "a crucial tool" for returning to sports after an injury or a period of inactivity. Given the high incidence of injuries in rugby players, calculating the injury incidence in this population and correlating it with FMS™ scores could provide valuable insights.
For this prospective study, forty amateur rugby players from various clubs in Normandy competing at the Federal 3 level will be recruited using a recruitment letter and a call for volunteers.
Each participant will perform two FMS™ (7 movements), at the beginning of the competitive season and at the end of the competitive season. The test will last 30 minutes per player. The initial interview will last 20 minutes. There will also be a follow-up of the players throughout the season to collect all injuries sustained by participants in the intervention.
The main expected outcome is a significant correlation (p < 0.05) between the FMS™ score and injury incidence. This correlation may then indicate a good predictive capacity of the FMS™, allowing it to be considered a predictive tool for injury risk.
To evaluate the correlation between two variables (injury incidence sustained by the player and the FMS™ score), the Spearman correlation coefficient will be used. This coefficient, if its value approaches -1 or 1, will indicate a good correlation between the player's injury incidence and their FMS™ score. Conversely, if the coefficient approaches 0, the correlation will be considered poor.
In a second phase, it is expected that a competitive season will directly affect the FMS™ score, highlighting the difficulty for an amateur player to maintain their physical capacities throughout an entire season.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Saint-Sébastien-de-Morsent, France, 27180
- Hôpital La Musse
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Players licensed with the French Rugby Federation (FFR): Their affiliation with the FFR requires a medical certificate confirming no contraindication to competitive sports practice.
- Players aged at least 18 years old, legally adults.
- Healthy players who have not sustained any musculoskeletal injuries or undergone surgical interventions in the past 6 months.
- Players competing in "Fédérale 3."
- Players from clubs based in Normandy.
Exclusion Criteria:
- Minor players
- Female players
- Players injured during the first interview or the first FMS™
- Players who are or have been professional athletes
- Players with a history of frequent serious injuries that could pose a risk to their continued participation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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FMS group
Each participant will perform two FMS™, one at the beginning of the competitive season.
The test will take 30 minutes per player.
The initial interview will last 20 minutes.
Players will also be monitored throughout the season to collect all injuries sustained by the participants in the study.
|
Each participant will perform two FMS™, one at the beginning of the competitive season.
The test will take 30 minutes per player.
The initial interview will last 20 minutes.
Players will also be monitored throughout the season to collect all injuries sustained by the participants in the study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The FMS™ Score
Time Frame: At the beginning of the season (baseline) for each player
|
The Functional Movement Screen™ (FMS™) is a tool designed to "evaluate an individual's functional movement patterns" and, according to its authors, can represent "a crucial tool" for returning to sport after an injury or a break from sports.
It consists of an assessment of seven so-called fundamental movements, which require good neuromuscular and motor control, as well as balance and stability.
These movements aim to place the evaluated subject in extreme positions to highlight significant imbalances throughout the body.
This test consists of a score from 0 to 3 for each of the 7 movements, and a final score out of 21 points.
The FMS reveals functional deficits by highlighting compensatory movements.
The higher the score, the fewer compensatory movements.
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At the beginning of the season (baseline) for each player
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Injuries
Time Frame: Through the season, up to 7 months per player
|
The secondary endpoint is the number of injuries.
An injury is defined as "any physical complaint caused by an energy transfer exceeding the body's ability to maintain its structural and/or functional integrity, sustained by a player, regardless of the need for medical treatment or the time lost due to the injury".
Here, only injuries involving time lost, the "time-loss injury," are considered.
Therefore, in this study, a player is considered injured if they are unable to participate in the following training session or match due to the injury.
Any other inability, such as personal or professional reasons, will not be considered.
This method of data collection is widely used in sports medicine due to its simplicity, even when athletes themselves report the injury.
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Through the season, up to 7 months per player
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024-A01804-43
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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