- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05005325
Functional Movement Screen Differences in Male and Female Footballers as an Injury Prevention Tool.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Functional movement screening (FMS) was developed by Cook et al. It evaluates range of motion, muscular imbalances and core strength by means of seven different movement. It is used to analyze the pattern of various fundamental movements and then highlights the limitations in that pattern and recognizes asymmetries in relation to that pattern of movement and eventually compares these inadequacies with outcomes that will improve a pragmatic approach to injury prevention. Prior studies reported that during pre-participation FMS can predict injuries in various athletes.
Several research studies carried out by researchers in this area have been involved in the exploring the strategies that can enhance the efficiency and performance of footballers in the field and investigate the effects of injuries on performance. Studies including FMS as an injury and evaluation tool have subjects which includes athletes playing multiple sports and generally involved male footballers, but the studies comparing scores of FMS among female footballers with male footballers are scarce. With advances in society and knowledge of participation in sports, more women participate in sports events, and the pre-participation and injury of this particular population should be explored. This research will discover this particular issue and bring to light the needs of female footballers and contributes to recognizing FMS as a predictive method for injury.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 46000
- Ra'ad Arena
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Male and Female Footballers
- Athletes training at least 3 times per week (>1.5h/week)
Exclusion Criteria:
- Recent injury of lower extremity within past 6 months
- History of traumatic brain injury
- History of concussion
- History of cervical spine injury within the last year
- History of shoulder surgery
- History of anterior cruciate ligament repair
- History of meniscal repair
- History of Achilles tendon repair
- History of ankle fracture
- Recent eye and ear disorders within past 6 months
- Receiving physical therapy for musculoskeletal injuries
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Experimental group(Male)
Participants will be included in the study after screening from inclusion criteria.
Each participant will perform FMS during a single session before competition as pre testing.
It consists of 7 movement tasks and 3 clearance screens.
Movement task will include deep squat, hurdle step, inline lunge, shoulder mobility, active straight-leg raise, trunk stability push-up and rotary stability.
Five of the 7 tasks (hurdle step, inline lunge, shoulder mobility, active straight-leg raise and rotary stability) will be performed on both right and left sides.
In addition to these, 3 clearance screen will assess the presence of pain with shoulder internal rotation/flexion, end range spinal flexion and end range spinal extension.
Participants will be instructed for each task performance and will perform 3 attempts for each task.
|
Hurdle steps Deep squats Inline lunges Shoulder Clearing Active straight leg raise Trunk stability pushup Rotary stability Spinal extension exam Spinal flexion exam
|
Experimental: Experimental group(Female)
Participants will be included in the study after screening from inclusion criteria.
Each participant will perform FMS during a single session before competition as pre testing.
It consists of 7 movement tasks and 3 clearance screens.
Movement task will include deep squat, hurdle step, inline lunge, shoulder mobility, active straight-leg raise, trunk stability push-up and rotary stability.
Five of the 7 tasks (hurdle step, inline lunge, shoulder mobility, active straight-leg raise and rotary stability) will be performed on both right and left sides.
In addition to these, 3 clearance screen will assess the presence of pain with shoulder internal rotation/flexion, end range spinal flexion and end range spinal extension.
Participants will be instructed for each task performance and will perform 3 attempts for each task.
|
Hurdle steps Deep squats Inline lunges Shoulder Clearing Active straight leg raise Trunk stability pushup Rotary stability Spinal extension exam Spinal flexion exam
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Functional Movement Screen
Time Frame: 6th week
|
Functional Movement Screen (FMS) will be used as a 'Pre' and 'Post' assessment tool to evaluate the risk of injury/dysfunctional performance among male and female footballers. Minimum and Maximum score interpretation required |
6th week
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Danish Latif, MSPT-SPT, Riphah International University
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
Other Study ID Numbers
- REC/0867 Fatima Amjad
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
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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