- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05206786
A Gluteus Maximus Strength Exercise Effectiveness for Improving Dynamic Postural Control in Female Basketball Players
Effectiveness of a Specific Strength Program of the Gluteus Maximus Muscle to Improve Dynamic Postural Control in Female Basketball Players
The study will be carried out at the Faculty of Nursing and Physiotherapy of the University of Alcalá. The study has been approved by the Animal Research and Experimentation Ethics Committee of the University of Alcalá. A total of 92 female basketball players aged between 12 and 25 will be selected and randomized in two different groups.
The control group will carry out a conventional preventive work out and the experimental group will carry out a specific strengthening program for the gluteus maximus in addition to the conventional preventive exercises.
The treatment will take place during the basketball club season and will last 4 months, from January to April 2022.
The objective is to evaluate the effectiveness of the inclusion of a specific gluteus maximus strength program in the conventional preventive work to improve the dynamic stability and to reduce the injury rate and pain in female basketball players.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Madrid
-
Alcalá De Henares, Madrid, Spain, 28801
- Sandra Sánchez
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Female basketball players belonging to a sports club.
- Female basketball players between 12 and 25 years old.
Exclusion Criteria:
- Acute lower limb injuries at the start of the study.
- Surgery on the lower limb in the previous year.
- Injuries or diseases that prevent the correct performance of the evaluation tests.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Control group. Conventional preventive work out
|
Female players in the control group will carry out a conventional preventive work that is organised in 3 training days per week.
First training session includes preventive strength and proprioception exercises.
Junior and senior teams (above 16 years old) will also do plyometrics exercises.
In the second training session, players will do preventive strength exercises with an increased load compared to the previous session and proprioception exercises.
Junior and senior players will also do anaerobic work.
In the third session, players will perform reaction speed exercises.
|
|
Experimental: Intervention group. Gluteus maximus strengthening specific program
|
Female players in the control group will carry out a conventional preventive work that is organised in 3 training days per week.
First training session includes preventive strength and proprioception exercises.
Junior and senior teams (above 16 years old) will also do plyometrics exercises.
In the second training session, players will do preventive strength exercises with an increased load compared to the previous session and proprioception exercises.
Junior and senior players will also do anaerobic work.
In the third session, players will perform reaction speed exercises.
Female players will carry out a gluteus maximus strengthening work out in addition to the control group programme. Of the following four exercises, the first and the third ones will be done on the first training session and the second and the fourth exercises will be done on the second one. Dosage will be 2 sets of 10 repetitions for each leg.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dynamic stability change assessed by a modified version of the Star Excursion Balance Test (SEBT). For this, Octobo-Balance device will be used.
Time Frame: Baseline and 4 months later
|
Five lower limb excursion directions are going to be analysed: anterior (SEBT-A), medial (SEBT-M), posterior (SEBT-P), posteromedial (SEBT-PM) and posterolateral (SEBT-PL), with all these excursion directions and the legs' length of each player we will calculate the sum of them.
The device system consists of an extending measuring tape magnetized to an octagon-shaped platform which allows to measure the different directions.
There is a marked point in the middle of the octagon where players must put one of their feet properly and push the measuring tape with the other one.
Players will have to go as far as possible in each direction without touching de floor or lifting the foot that it's set on the octagon.
There will be three attempts in all the excursion directions, and it will be done for each leg.
|
Baseline and 4 months later
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in the rate of lower limb injuries measured with a Daily Injury Report
Time Frame: Daily from baseline until the end of the research study 4 months later
|
Lower limb injuries occurrence will be recorded on a daily basis.
For this purpose, one person in charge of each team, under the supervision of the researchers, will fill in an injury report.
This report will include basic information about the injury, so as the location, the side of the body, the type and the mechanism of the injury and the time of injury, as well as the happening and duration of a sick leave.
|
Daily from baseline until the end of the research study 4 months later
|
|
Pain change measured with the Visual Analogue Scale
Time Frame: Baseline and 4 months later
|
Players will be asked to rate from 0 to 10 their general pain and their specific pain in: ankle, knee, hip and low back.
|
Baseline and 4 months later
|
|
Vertical Jump Height using the app MyJump2
Time Frame: Baseline and 4 months later
|
Vertical jump is calculated analysing it on a recorded video with the help of this app.
It is necessary to select manually the take-off frame and landing frame.
Videos will be recorded by the researchers in the frontal plane in the same position and distance from the jumping player.
Participants will be taught to perform a correct vertical jump, starting from a static position with knees and hips at 90º and the hands on the hips, as well as stretching the knees during the flight and landing.
The objective is to achieve the maximum height with the jump.
Total leg length (from anterior iliac spine to tiptoe in maximum plantar flexion) and height with flexed knees at 90º (measured vertically from floor to greater trochanter) will be measured to calculate the height of vertical jumps with the help of the app.
|
Baseline and 4 months later
|
|
Dynamic knee valgus measured with the programme Kinovea
Time Frame: Baseline and 4 months later
|
Players will be recorded from the frontal plane and in the same position for each player.
Players shall perform three jumps in a row.
Afterwards, with the Kinovea programme, the moment in which the highest knee valgus is produced in the landing of the different jumps will be analysed.
|
Baseline and 4 months later
|
|
Treatment adherence through an exercise tracking diary
Time Frame: Weekly from baseline until the end of the research study 4 months later
|
Players will be required to fill in a sheet in which they will be requested for whether or not they have done the corresponding exercises during the week.
|
Weekly from baseline until the end of the research study 4 months later
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sandra Sánchez, University of Alcalá, Madrid, Spain
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
Other Study ID Numbers
- CEIM/2021/6/130
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.
Clinical Trials on Basketball
-
Riphah International UniversityRecruitingBasketball PlayersPakistan
-
Universidad Católica San Antonio de MurciaCompletedBasketball PlayersSpain
-
University of Las Palmas de Gran CanariaCompleted
-
Riphah International UniversityCompleted
-
Investigación en Hemofilia y FisioterapiaWithdrawn
-
Biruni UniversityRecruiting
-
Birjand University of Medical SciencesCompletedBasketball PerformanceIran
-
Kutahya Health Sciences UniversityCompletedBasketball PlayersTurkey
-
Investigación en Hemofilia y FisioterapiaWithdrawnBasketball PlayersSpain
-
Hasan Kalyoncu UniversityCompleted
Clinical Trials on Conventional preventive work out
-
Assiut UniversityCompletedEPO Teqnique in Fetal Head ExtractionEgypt
-
Riphah International UniversityCompletedRespiratory RehabilitationPakistan
-
Columbia UniversityPatient-Centered Outcomes Research Institute; NYU Langone Health; Alzheimer's... and other collaboratorsCompletedDepressive Symptoms | BurdenUnited States
-
VA Office of Research and DevelopmentActive, not recruitingSarcopeniaUnited States
-
University Hospitals Cleveland Medical CenterRecruitingHip Injuries | ACL InjuryUnited States
-
American University of Beirut Medical CenterRecruitingPediatric ALL | Anesthesia | Cardiac ComplicationLebanon
-
Cairo UniversityCompletedZygomatic FracturesEgypt
-
University of Sao PauloRecruitingPeriodontitis | Type 2 Diabetes | HalitosisBrazil
-
University of ChicagoNational Human Genome Research Institute (NHGRI)Recruiting