- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03862508
Plyometric Work Together With the Use of Ballast Weight in Lower Limbs in the Improvement of Performance in Jumpers (PLIO)
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
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Comunity Of Madrid
-
Madrid, Comunity Of Madrid, Spain, 28670
- Universidad Europea de Madrid
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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:
|
|
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
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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