- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06551532
"Ecological Program Changes Pelvic Kinematics in Soccer Players: Pilot Study on Hamstring Injury Implications"
August 9, 2024 updated by: Andrea Astrella, RX2 Sports and Health
An In-season Ecological Program Performed by Soccer Players Changes Pelvic Kinematics During Static, Linear Sprinting and Sport-specific Tasks: a Pilot Study on the Implication for Hamstring Injuries.
The present pilot study aimed to investigate whether a 6-week multicomponent intervention, comprising a structural lumbopelvic and sprint technique program, could reduce anterior pelvic tilt in soccer players who regularly participated in soccer practice.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This pilot study aimed to evaluate the impact of a 6-week multicomponent intervention combining lumbopelvic control exercises and running technique training on pelvis structure and lower limb kinematics in semi-professional soccer players.
Seventeen players were randomly assigned to a control group (CG) or an intervention group (IG).
Data on static anterior pelvic tilt (APT) and three-dimensional kinematics during high-speed running (HSR) and high-speed soccer running (HSSR) were collected before (PRE) and after (POST) the intervention period.
Study Type
Interventional
Enrollment (Actual)
17
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Madrid, Spain, 28223
- RX2 Sports and Health
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- The inclusion criteria for both groups were: (a) being between 18 and 40 years old, and (b) being available for their teams
Exclusion Criteria:
- Exclusion criteria for both groups included (a) not having suffered any musculoskeletal injuries in the previous 3 months and (b) not being involved in any additional strength program outside of their regular team training.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Multicomponent Intervention Group
Soccer players in the intervention group (IG) underwent a multimodal training program comprising 3 sessions per week for 6 weeks.
All the soccer players in IG were allowed to continue their usual training (5 sessions per week) and matches (1 per week) at their clubs.
The training program comprised both lumbopelvic training (foam rolling, manual therapy, mobility, posture, and strength training) and sprint technique components.
The intervention included a total of 18 sessions of approximately 50 minutes each and sessions were supervised by 2 physiotherapists.
During the 6 weeks of the intervention, participants performed the multicomponent program 3 times a week.
Monday, Wednesday, and Friday were the chosen days for carrying out the training program, as Sunday was usually a game day.
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Lumbopelvic training (foam rolling, manual therapy, mobility, posture, and strength training) and sprint technique program.
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No Intervention: Control Group
Soccer players in the control group (CG) were requested not to modify their established training routines during the entire 6-week period.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anterior Pelvic Tilt (APT) Reduction.
Time Frame: Baseline (PRE) and immediately after 6 weeks of intervention (POST).
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The primary outcome measure is the reduction in static anterior pelvic tilt (APT) immediately after 6 weeks of the multicomponent intervention.
APT is measured using a three-dimensional kinematic analysis during static and high-speed running tasks.
The reduction in APT will be assessed before (PRE) and immediately after (POST) the intervention period to determine the effectiveness of the intervention in modifying pelvic alignment.
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Baseline (PRE) and immediately after 6 weeks of intervention (POST).
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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biomechanical variables during high-speed running (HSR) and high-speed soccer running (HSSR) tasks
Time Frame: Baseline (PRE) and immediately after 6 weeks of intervention (POST).
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"This outcome measure assesses changes in specific biomechanical variables, including segment orientations (trunk, pelvis, femur, and tibia) relative to the sagittal plane, and joint angles (hip flexion and knee flexion) during high-speed running (HSR) and high-speed soccer running (HSSR) tasks.
The study aims to evaluate the shift towards a more front-side oriented sprint technique model and the associated improvements in sprint performance time.
Measurements will be taken using three-dimensional motion capture analysis to quantify the kinematic changes during HSR and HSSR."
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Baseline (PRE) and immediately after 6 weeks of intervention (POST).
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 6, 2023
Primary Completion (Actual)
June 8, 2023
Study Completion (Actual)
August 7, 2024
Study Registration Dates
First Submitted
August 7, 2024
First Submitted That Met QC Criteria
August 9, 2024
First Posted (Actual)
August 13, 2024
Study Record Updates
Last Update Posted (Actual)
August 13, 2024
Last Update Submitted That Met QC Criteria
August 9, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- RX2_EstudioHamstring_2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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