Plyometric and Eccentric Training in Improving the Strength, Stability and Ability of Women Soccer Players

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

Efficacy of Plyometric and Eccentric Training in Improving the Strength, Stability and Ability of Women Soccer Players. A Randomized Pilot Study.

Introduction. The high rate of recurrence and clinical involvement of muscle injuries in lower limbs, makes the hamstring musculature a very important structure in the development of athletes. Excentric movements, where eccentric force and flexibility are fundamental, and the quadriceps-hamstrings contraction cycle are risk factors for hamstring muscle injury.

Aim. ascertain the effectiveness of plyometric and excéntric exercises in the improvement of hamstring strength.

Study design. Randomized, prospective, multicenter, single-blind clinical study with athletes.

Methods. This study will be carried out with a sample of 40 women, federated players from 18 to 30 years old. They will be randomized into two groups: experimental (plyometric work and eccentric exercises) and control (eccentric exercises). The intervention will last 6 weeks in which, before each training, they will carry out the intervention, for 20 minutes, 3 days a week. An inter-judges piloting will be carried out. We will analyze the normality of the sample with the Kolmogorov-smirnov test and for the inferential analysis, we will use the t-student test of paired data to observe the difference between each evaluation in each study group, and the repeated measures ANOVA to calculate the effect intra and intergroup. Using Cohen's formula we will calculate the size of the effect.

Expected results. The eccentric work along with the plyometrics improves strength in hamstrings, jumping and stability.

Study Overview

Status

Completed

Conditions

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

      • Madrid, Spain
        • European University of 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 30 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Women
  • 18 to 30 years old
  • With 3 or less days of training a week
  • Federate in the Community of Madrid (Spain)

Exclusion Criteria:

  • Players who are injured and cannot do the job at the time of the study
  • Soccer players who have had a hamstring injury in the last 6 months
  • To practice another sport
  • They are receiving physiotherapy treatment in the lower limb
  • Not signing 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: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Experimental group
Leg Squat Lounge: The player will be placed in squat position and her partner will be placed behind, suspending the most posterior leg in the air. With the leg that is supported, you will perform a monopodal jump with controlled fall, supporting the foot from tip to heel. It will be done with both lower limbs performing 1 series of 5 repetitions with 30 seconds of rest between sets. 180 jump: The footballer will start in bipodal support, with the trunk erect and hands on the hips. Perform a bipodal jump with a 180º turn during this, keeping the fall for 2 seconds. Each repetition, the turn will be done in a different sense. It will carry out 2 series of 20 sec of execution with 20 sec of rest between series. Brad jump stick landing: The player will stand in hands-free standing. Perform a bipodal jump as far as possible. The knees will not exceed the tip of the foot and the fall will be with a trunk position as straight as possible. He will make 5 jumps the first two weeks.
The players assigned to the experimental group will receive an intervention through plyometric and eccentric hamstring exercises
ACTIVE_COMPARATOR: Control group

Nordic Funds: One player will stand on her knees, while the other, behind, fixes her legs. The kneeling footballer must drop forward in a controlled manner until she touches the ground and returns to the starting position. The Diver: Player in monopodal support on the lower limb to work, performing hip flexion with the arms forward and the opposite lower limb back, looking for a horizontality in the pelvis (with 10º-20º knee flexion) It will be done with both lower limbs.

The Glider: With the footballer standing in front of her partner, holding both of them by the shoulders, she lets one leg slide back while the other stays fixed. To return to the starting position, it will be helped by the other player, while the knee will not exceed 10 degrees of flexion. The distribution of all the exercises will be: 2 sets of 5 repetitions with 20 sec rest between sets

The subjects included in the control group will perform an eccentric work protocol

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline hamstring strength after treatment and at 1 month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The mobile application "Nordic" will be used to assess the strength of the hamstring muscles. With the athlete kneeling on the floor, fixed by a partner from the ankles, she will drop down forward. The evaluator will be on the side, recording with a smartphone (Iphone 7) to measure the moment when the subject uncrosses the arms. The test will be carried out up to three times, taking the measures of the angle of rupture in the exercise (angle that forms the trunk with the ground considering the position of the tibiae). The unit of measure the breaking angle.
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 the jump after treatment and at 1 month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
With the mobile application "My jump 2.0" the jump will be measured. The athlete will be located 1.5 meters from the evaluator, who will be in front of her with a mobile (iPhone 7 model) at ground level. The test will consist of the realization of a Counter Movement Jump (CMJ). The unit of measure of the jump of the application will be the Newton.
Screening visit, within the first seven days after treatment and after one month follow-up visit
Change from baseline lower limb stability after treatment and at 1 month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
With the Y-Balance test the lower limb stability will be measured. The player will be placed in the center of an inverted Y-shaped figure, and in monopodal support on the leg to be evaluated. 3 attempts will be made for each of the scopes (anterior, posteromedial and posterolateral). The distance will be measured in centimeters, taking as value the arithmetic mean of the three attempts made in each range. The Y-shaped figure will be made with tape on the floor. The distance calculation will be carried out with a tape measure.
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)

February 10, 2020

Primary Completion (ACTUAL)

April 30, 2020

Study Completion (ACTUAL)

May 10, 2020

Study Registration Dates

First Submitted

February 1, 2020

First Submitted That Met QC Criteria

February 3, 2020

First Posted (ACTUAL)

February 5, 2020

Study Record Updates

Last Update Posted (ACTUAL)

September 2, 2021

Last Update Submitted That Met QC Criteria

September 1, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • HAM-EXPL

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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