Elastic-explosive Strength Training Combined With Active Joint Mobilizations in Basketball Players

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

Efficacy of a Physiotherapy Intervention Through an Elastic-explosive Strength Training Combined With Active Joint Mobilizations, on the Improvement of the Efficiency of Repeated Vertical Jumping in Basketball Players

The specific training of the elastic-explosive force of the muscles involved in vertical jump and active mobilizations is used to improve the quality of the jump. It is also intended to reduce the loss of centimeters, recovery times and fatigue produced during a series of vertical jumps.

The objective of the study is to assess the effectiveness of active mobilizations together with specific training in lower limbs, in ankle mobility, the perception of effort and the height and resistance of vertical jumping in amateur basketball players.

Randomized clinical study. 50 basketball players from 20 to 35 years will be randomized to the study groups: control group (resistance strength exercises, elastic-explosive force) and experimental group (resistance strength exercises, elastic-explosive force together with active mobilizations). The dependent variables will be: repeated jump (15 second Jump test, my Jump 2), maximum vertical jump (CMJ free arms, my Jump 2), subjective perception of effort (Borg scale) and ankle dorsiflexion (goniometer). The sample distribution will be calculated using a Kolmogorov-Smmirnof analysis. 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.

It is expected to observe an improvement in the resistance of vertical jumps, with a decrease in the loss of centimeters in the repetitions of jumps.

Study Overview

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

Male

Description

Inclusion Criteria:

  • Basketball players in the Community of Madrid
  • Male
  • With an age range of 18 to 35 years
  • Federated

Exclusion Criteria:

  • Athletes who present an injury at the time of the study
  • Who are receiving some parallel physiotherapy intervention
  • Have an injury during the experimental or follow-up phase
  • 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 of the intervention will have a duration of 15 minutes of specific training taking place two sessions a week, during a period of 5 weeks. The exercises will be performed in the first 15 minutes of the training session. The intervention will include specific exercises of elastic-explosive strength and resistance strength

The resistance exercises are: running (3 minutes), 2 farmers carrying marching, 3 side to side ankle hops, 4 plyo lunge jump, 5 lateral jump over barrier, 2 monopodalic jump with ball pass, 3 board throw with half court sprint, 4 lateral shuffle mirror, and 5 combo finisher 4x4.

Plyometric exercises are: ankle rotations, knee extension, squat, hip flexion-extension, knee and ankle, ankle mobilizations, squat with rise, pelvis ante / retroversion, global mobilization, stride

Active Comparator: Control group
Each session of the intervention will have a duration of 10 minutes of specific training taking place two sessions a week, during a period of 5 weeks. The exercises will be performed in the first 15 minutes of the training session. The intervention will include specific exercises of elastic-explosive strength
Plyometric exercises are: ankle rotations, knee extension, squat, hip flexion-extension, knee and ankle, ankle mobilizations, squat with rise, pelvis ante / retroversion, global mobilization, stride

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline maximum 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
The My Jump 2 application will be used. With the video we can see the moment when the feet do not touch the ground and with this data the application automatically calculates the height in centimeters. From a squat position, the player will have to perform a vertical jump, landing in the same starting position.
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 resistance of the explosive force after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The 15 sec repeated jump test will assess the resistance of the explosive force. With the My Jump 2 application we will calculate the height in repeated jumps in 15 seconds. To do this, we will ask the athlete to, from a squat position, perform 15 repeated vertical jumps, returning to the starting position every time.
Screening visit, within the first seven days after treatment and after one month follow-up visit
Change from baseline subjective perception of effort after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
We will use the modified Borg scale with a scoring range of 1 to 10 points (the higher the score, the greater the perception of effort). The concept of perceived effort is a subjective assessment that indicates the person's opinion regarding the intensity of the work performed. 1 indicates little fatigue, 10 is the maximum effort perceived by the athlete
Screening visit, within the first seven days after treatment and after one month follow-up visit
Change from baseline dorsal ankle flexion after treatment and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
This variable will be measured with the use of a goniometer. With the athlete standing, from a stride position, with the first finger placed 10 cm from the wall, we will ask him to do a knee flexion towards the wall, with the heel always resting on the floor. We will place the goniometer axis in the center of the outer malleolus. The fixed arm will be parallel to the ground, while the mobile arm will be aligning the fibula. The unit of measure is the degrees.
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 30, 2020

Study Completion (Actual)

June 10, 2020

Study Registration Dates

First Submitted

February 27, 2020

First Submitted That Met QC Criteria

February 27, 2020

First Posted (Actual)

February 28, 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

  • Jump

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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