Plyometric Work Together With the Use of Ballast Weight in Lower Limbs in the Improvement of Performance in Jumpers (PLIO)

January 23, 2020 updated by: Investigación en Hemofilia y Fisioterapia

Efficiency of Plyometric Work Together With the Use of Ballast Weight in Lower Limbs in the Improvement of Performance in Jumpers From 18 to 40 Years Old. Nonrandomized Pilot Study.

Introduction. The high jump is a discipline that use the shortening-stretching cycle. Plyometric exersices emply an eccentric load followed by concentric contraction. Powerinstep is a tool training by means of weigthed weigth whose objective is improving performance in athletes.

Aim. Evaluate efficacy of plyometric training with Powerinstep® in lower limbs, in the performance improvement in professional height jumpers from 18 to 40 years old.

Study design. Non-randomized clinical trial, single bind, with follow-up period.

Methods. 20 athletes will be recruited, that will be randomized to the two study groups: experimental (they carry out a plyometric training programme with Powerinstep) and control (won't be made a intervention on the subjects included in this group). The intervention consists of 6 week, with 2 session for week of 15 minutes duration each. The dependent variables will be the height of the jump, the time of flight, the reaction speed and the impulse force, measures though a pressure platform (model T-PLATE), employing Countermovement Jump, Abalakov and Drop Jump tests. We will make a descriptive statistical analysis. The Shapiro-Wilk statistical test will be used to calculate normality. Trough t-student test of repeated measures and an ANOVA of repeated measures will be calculated the difference between distinct assessment (preintervention, postintervention and follow-up) and the effect intra and inter subject, respectively.

Expected results. We want to observe the changes in performance improvement in height jumpers.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

20

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 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Height jumpers
  • Age between 18 and 40 years
  • Currently participate in the competitive field

Exclusion Criteria:

  • Present medical diagnosis of musculoskeletal pathology
  • Who have not had musculoskeletal injuries in the last month
  • 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: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental
Five Plyometric exercises

Jump Drop Jump, dropping the subject from a height of 30cm and then make a vertical jump.

Long jumps asking the athletes to take momentum and make a leap forward trying to reach the greatest possible distance.

Jump Countermovement jump unilaterally, alternating the lower extremities. Jumps 180º with the athletes maintaining a semi-squat position. Jump Countermovement jump repeatedly starting from an upright position and the upper extremities in both hips.

All the exercises will be done through 8 repetitions per session during the first two weeks, increasing two repetitions every two weeks (until reaching 12 repetitions at the end of the intervention).

For the realization of each one of the exercises, the ballasted weight will be used (Powerinstep® model).

Other Names:
  • Plyometric training programme with Powerinstep
No Intervention: Control
Subjects included in the control group will not receive any intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from baseline jump height after intervenion and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The height of the jump will be measured on the Countermovement Jump test. The evaluating physiotherapist will stand in front of the subject, who will start from an upright position with the arms on both hips, and will go to a position of flexion of lower members at 90º. Finally, we will ask the subject for a vertical jump on the pressure platform. The results of this test are measured in centimeters and the higher the score, the greater the vertical jump capacity.
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 impulse force after intervention and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The impulse force will be measured with the Abalakov test. The evaluator will be placed in front of the evaluated, previously in an upright position, asking him to go to a position of flexion of lower limbs of 90º and then, assisted by the impulse of the arms, perform a jump on the pressure platform. The unit of measurement of the results of this test is the Newton, indicating a higher score indicates a greater impulse of the jump.
Screening visit, within the first seven days after treatment and after one month follow-up visit
Change from baseline vertical jump after intervention and at month
Time Frame: Screening visit, within the first seven days after treatment and after one month follow-up visit
The vertical jump will be measured with the Drop Jump test. In this test, the physiotherapist will stand in front of the subject, who in an upright position will be dropped from a height of 30 centimeters on the pressure platform, then performing a vertical jump with the help of the arms. The results, in this test, are measured in centimeters, where a higher score indicates a greater vertical jump.
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 4, 2019

Primary Completion (Actual)

March 15, 2019

Study Completion (Actual)

June 1, 2019

Study Registration Dates

First Submitted

February 27, 2019

First Submitted That Met QC Criteria

March 4, 2019

First Posted (Actual)

March 5, 2019

Study Record Updates

Last Update Posted (Actual)

January 27, 2020

Last Update Submitted That Met QC Criteria

January 23, 2020

Last Verified

January 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • PLIO project

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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