Bulgarian Squat in the Improvement of Asymmetries of Lower Limbs in Soccer Players

September 1, 2021 updated by: Investigación en Hemofilia y Fisioterapia

Efficacy of the Bulgarian Squat in the Improvement of the Asymmetries of Lower Limbs Improving the Strength in the Hamstrings and Stability of the Knees in Soccer Players. A Randomized Clinical Study.

1541/5000 The aim of the Bulgarian squat is to improve the hamstring strength and the stability of the knees, thus reducing asymmetries in the lower limbs. It consists in achieving greater strength and stability of the lower limbs to adapt the athlete to the demands of training and competitions as safely as possible.

The main objective of the study is to assess the effectiveness of the Bulgarian squat, in the improvement of asymmetries in lower limbs; improving hamstring strength and knee stability.

Randomized, simple blind clinical study. 30 soccer players will be randomized to the study groups: experimental (Bulgarian squats) and control (non-intervention team routine). The treatment will last 4 weeks, with 2 weekly sessions of 10 minutes each. The study variables will be: lower limb strength (vertical jump with the My Jump 2 application), lower limb stability (Y ™ -Balance test) and lower limb asymmetries (Triple Hop Test, Single Hop Test for Distance and Functional Movement Screen) The normality of the sample will be calculated using the Kolmogorov -Smirnof test. The changes after each evaluation will be analyzed with the t-student test and with an ANOVA of repeated measures, the intra and intersubject effect will be observed. The effect size will be calculated using Cohen's formula.

An improvement in the strength, stability and asymmetries of the lower limbs in soccer players is expected.

Study Overview

Status

Withdrawn

Conditions

Intervention / Treatment

Study Type

Interventional

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

    • Comunity Of Madrid
      • Madrid, Comunity Of Madrid, Spain, 28670
        • Universidad Europea de Madrid

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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Female players
  • With an age range of 18 to 35 years
  • Federated in the Community of Madrid
  • That at the time of the study do not suffer any injury

Exclusion Criteria:

  • Athletes who have not undergone surgery on the lower limbs in the last three months
  • Who have not taken muscle relaxants in the last three days
  • Who have not understood or have a lack of understanding about the intervention
  • Have not signed the informed consent document

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental group

Each session will last 10 minutes, taking place two days a week, over a period of four weeks. The intervention will take place at the beginning of the training session.

The players included in the experimental group will perform an exercise protocol with Bulgarian squats.

The intervention using Bulgarian squat exercises will consist in the application of the protocol described by Aguilera-Castells et al. The technique will be done with the footballer standing. The athlete with one foot in front and the other behind the body, arms crossed over her chest, and her upper body, will remain upright with a natural swing in the lower back during the entire exercise. The players will lower the body (eccentric phase) until the front knee flexes to 90º. Subsequently, they will return to the initial position with a full extension of the knee of the front leg (concentric phase), maintaining an erect trunk position. The front foot will be placed in a fixed position contacting the ground, and the rear foot will rest on a horizontal press bench.
No Intervention: Control group
The players included in the control group will continue with their usual warm-up routine.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline hamstring muscle strength after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
It will be done through the vertical jump Through the Appstore My Jump 2. The athlete will stand in standing position with the feet in parallel with a separation corresponding to the height of her hips. It will start with a knee flexion of 90º and with the arms along the body. You will be asked to perform a jump by bringing the lower limbs to a triple flexion (hip, knees and ankles). At the same time that it is pushed by pressing on the heels, it will take the arms in the take-off phase above its head. The load will be introduced if there is, in kg, and we will obtain the force time data (in Newton).
Screening visit, within the first seven days after treatment and after one month follow-up visit

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline stability after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
It will be done with the Y-Balance test. The athletes will be placed in standing position in monopodal support with a slight knee flexion in the starting platform that consists of two rear pipes that will be placed at 135º from the previous pipe with 45º between the 2 back pipes. Barefoot athletes, with the support foot behind the red line of the central starting platform, will be asked to bring the leg that is not in support to the platforms located in the anterior and posterior tubes and slide them off continuous way and without bouncing as far as you can. Six trials will be performed on each leg in each of the three directions using the highest scores for analysis. The unit of measure of this instrument is centimeters: a higher score indicates greater stability, strength and proprioception.
Screening visit, within the first seven days after treatment and after one month follow-up visit
Change from baseline asymmetries of lower limbs after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
With the Single Hop Test for Distance we will assess the ability of the player to make a maximum monopodal jump, measuring its distance in cm. A strip of tape 15 cm wide and 6 m long perpendicular to the starting line will be placed and the athlete will rest on one leg and with her foot on the line that marks the exit by performing a maximum horizontal jump, and receiving with the same leg The arms have to be throughout the hip test, not being able to use them to improve the jump. The distance will be measured from the starting line to the back of the heel. The athlete must maintain the position after the jump for at least 3 seconds without losing balance or supporting the other leg so that the repetition is counted. In case of not fulfilling said quality criteria in the execution, the jump will be repeated after the established recovery time.
Screening visit, within the first seven days after treatment and after one month follow-up visit

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

March 2, 2020

Primary Completion (Actual)

May 20, 2020

Study Completion (Actual)

June 10, 2020

Study Registration Dates

First Submitted

February 25, 2020

First Submitted That Met QC Criteria

February 25, 2020

First Posted (Actual)

February 26, 2020

Study Record Updates

Last Update Posted (Actual)

September 5, 2021

Last Update Submitted That Met QC Criteria

September 1, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

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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