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Football PlayerNCT04289896

Plyometric Training, in the Improvement of Explosive Strength and Speed in Soccer Players

A study testing Plyometric exercise in people with Football Player, run by Investigación en Hemofilia y Fisioterapia at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Football requires a high number of actions at high speed and intensity. The application of plyometrics can improve explosive strength and speed levels in soccer players. The main objective of the study is to assess the effectiveness of a program based on plyometric exercises for the improvement of the explosive force… Read more about this study

Who is it for?
Ages 18 to 30 years, men onlyHealthy volunteers can take part
Conditions the study is for
Football Player
What is being tested?
Plyometric exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
17 participants
Where
1 siteSpain
Study dates
2 Mar 2020to 10 Jun 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Youth soccer players federated in Castilla y León
  • Over 18 years
  • Male
  • That they train at least twice a week.

Who cannot join

  • subjects who: present a medical diagnosis of musculoskeletal lesion in the lower limb at the time of starting the study
  • Who have been out of the competition for more than 6 months as a result of an injury in the last year
  • That are part of the experimental phase of another study during our intervention and follow-up period
  • That they do not attend at least 80% of the intervention sessions
  • Not sign the informed consent document.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Universidad Europea de Madrid

    Madrid, Comunity of Madrid, 28670

Other trials in Spain

About this study

Official title: Effectiveness of an Intervention Through a Plyometric Training Program, in the Improvement of Explosive Strength and Speed in Youth Players. A Randomized Clinical Study.

Football requires a high number of actions at high speed and intensity. The application of plyometrics can improve explosive strength and speed levels in soccer players.

The main objective of the study is to assess the effectiveness of a program based on plyometric exercises for the improvement of the explosive force in vertical jump and the speed in running with and without the ball in soccer players of youth category.

Read more

Randomized clinical study, simple blind, with follow-up period. 30 players will be randomized to the study groups: experimental and control. The intervention will last 4 weeks, with 2 weekly sessions lasting 20 minutes. The study variables will be: Vertical Countermovement Jump Test with Arms and Twenty-Centimeter Drop Jump Reactive Strength Index (Explosive Force), running speed without ball and ball (20 meter speed test), hitting speed of ball (Maximal Kicking Velocity Test), hamstring extensibility (Sit and Reach Test) and sural triceps extensibility (Leg Motion Basic). Normality will be calculated using an analysis of Kolmogorov Smirnov. With the t-student test the differences between assessments will be calculated and with an ANOVA of repeated measures, the effect between intersubject will be calculated. The effect size will be obtained with Cohen's formula.

It is expected to obtain an improvement in the explosive force in the vertical jump, as well as in the running speed with and without the ball.

Conditions
Football Player
Being tested
Plyometric exercise
Keywords
Football, Youth players, Plyometric exercises, Strength, Running speed, Muscular extensibility, Youth players

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Plyometric exerciseOther

    The plyometric program to be followed by the subjects assigned to the experimental group during the four weeks includes: Squat jumps, alternate lunge, cyclic horizontal jump, horizontal left leg jump, horizontal right leg jump, vertical left leg jump, right leg vertical jump, squat box jumps, box jumps left leg, box jumps right leg, box to box squat jumps, box to box left leg, box to box right leg.

    In all the exercises the subjects will be able to help themselves with the arms and a rest period of 120 seconds will be left between each series.

    The intervention will be carried out prior to training, keeping a minimum of 48 hours of rest between sessions.

Study groups in NCT04289896
Study groupRoleWhat they receive
Experimental groupExperimentalEach session will last 20 minutes, taking place 2 days a week, for a period of 4 weeks. Prior to the completion of the routine training of each team, the plyometric exercise program will be carried out in the experimental group. When the intervention ends, the members of the experimental group will perform the usual training
Receives: Other: Plyometric exercise
Control groupNo interventionAthletes included in the control group will not perform any intervention, continuing with their usual routine.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from baseline explosive force in vertical jump after treatment and at month

    Through the Vertical Countermovement Jump Test with Arms. The subject will be placed in standing position on a contact platform, it should make a rapid downward movement followed by a maximum vertical jump using the arms. The distance jumped in centimeters will be measured.

    Measured: Screening visit, within the first seven days after treatment and after one month follow-up visit

Secondary outcomes (4)
  1. Change from baseline running speed after treatment and at month

    A speed test of 20 meters will be carried out on a flat surface of grass, which will be carried out both with a ball and without a ball. Initially, there will be a specific warm-up of 3 sub-maximum races in those 20 meters, after which, the subjects will make 3 maximum sprints of 20 meters, with 3 minutes of rest between them. The race will start with the subject 0.5 meters behind the starting line. The time it takes for the subject to arrive from the start line to the 20 meter line will be measured. The fastest sprint time of the 3 attempts will be selected.

    Measured: Screening visit, within the first seven days after treatment and after one month follow-up visit

  2. Change from baseline ball hitting speed after treatment and at month

    Through the Maximal Kicking Velocity Test. Each subject will hit a soccer ball located on the ground, instructing them to obtain maximum speed. They must strike with maximum force towards a net with the dominant leg and with a run of 2 strides. The distance between the ball and the net will be 4 meters. Each subject will make 2 practice strokes and 3 strokes of maximum strength, among which 1 minute rest will be allowed. The speed of the ball will be measured with a radar placed 2 meters from the ball and 0.7 meters from the ground

    Measured: Screening visit, within the first seven days after treatment and after one month follow-up visit

  3. Change from baseline hamstring extensibility after treatment and at month

    It will be done by applying the Sit and Reach Test. This test will be carried out with the subject seated, knees extended and the feet in 90º of flexion placed both, against a drawer designed for the realization of this test. From this position, the subject is urged to progressively and maximally flex the trunk with the legs and arms extended while maintaining the final position for 2 seconds. The final position is the result of the test, assessing at that time the distance (in centimeters) that exists between the tips of the fingers and the tangent to the soles of the feet

    Measured: Screening visit, within the first seven days after treatment and after one month follow-up visit

  4. Change from baseline sural triceps extensibility after treatment and at month

    An assessment of the dorsiflexion of the ankle under load will be performed. It will be used as a measuring instrument Leg Motion Basic. The subject will be placed in standing position (arms crossed on the chest) with the foot to be assessed in advance on the work surface, respecting the marks of this. You should perform an ankle dorsiflexion forward the knee while moving the vertical reference on the platform. It is important to ensure that the subject does not detach the heel from the floor during the test

    Measured: Screening visit, within the first seven days after treatment and after one month follow-up visit

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Feb 2020
  2. Study start2 Mar 2020
  3. Primary completion20 May 2020
  4. Study completion10 Jun 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
17 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04289896
Sponsor's protocol ID
PLYO
Status last verified
Sep 2021
First submitted
27 Feb 2020
Last updated
2 Sep 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Plyometric exercise in people with Football Player, run by Investigación en Hemofilia y Fisioterapia at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 2 Sep 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from baseline explosive force in vertical jump after treatment and at month (time frame: Screening visit, within the first seven days after treatment and after one month follow-up visit). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Sep 2021.

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