Acute Effect of Plyometric Exercises on Musculotendinous Properties
1 other identifier
interventional
30
1 country
1
Brief Summary
Preventive and rehabilitation programs include plyometric exercises to promote agility, power, and muscle activation pattern during jumping. These exercises also are known to cause a high mechanical load that increases the risk of a musculoskeletal injury. The knowledge regarding the musculoskeletal damage result from this configuration of exercise can help to elaborate safer and effective training and rehabilitation programs. In this study, the investigators will conduct a clinical trial to determine the acute effect of plyometric exercises on damage caused on different portions of quadriceps and biceps femoral's muscles and tendons of quadriceps, and biceps femoral, and its effects on mechanical properties.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable healthy
Started Feb 2020
Longer than P75 for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 13, 2020
CompletedFirst Posted
Study publicly available on registry
February 18, 2020
CompletedStudy Start
First participant enrolled
February 20, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 5, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2022
CompletedNovember 5, 2020
November 1, 2020
1.6 years
February 13, 2020
November 4, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Change from baseline of echo intensity of quadriceps and biceps femoral muscles
Muscle echo intensity will be assessed for transversal and longitudinal ultrasonography images.
Baseline, immediately after exercise and up to 48 hours exercise
Change from baseline stiffness of patellar tendon
Patellar tendon stiffness during 5 seconds rampa contraction protocol. Patellar tendon stiffness will be estimate from force/deformation relationship of tendon.
Baseline, immediately after exercise and up to 48 hours exercise
Change from baseline young modulus of patellar tendon
Patellar tendon young modulus during rampa contraction protocol. Young modulus will be estimate from force/deformation relationship of tendon normalized to transverse section area of tendon.
Baseline, immediately after exercise and up to 48 hours exercise
Secondary Outcomes (1)
Change from baseline echo intensity of quadriceps and biceps femoral tendons
Baseline, immediately after exercise and up to 48 hours exercise
Other Outcomes (1)
Change from baseline muscle soreness of quadriceps and biceps femoral muscles
Baseline and up to 48 hours exercise
Study Arms (1)
Plyometric exercise
EXPERIMENTALInterventions
Plyometric exercises will be composed of vertical jumps, box jumps, half squat jumps, high straight jumps, bounding jumps, drop jumps and 10-m sprint.
Eligibility Criteria
You may qualify if:
- Who practice physical activity (except jump training);
- No previous lower extremity muscle injury at least 6 months before the recruitment;
- No previous lower extremity ligament or tendon injury or surgery;
- No auditory, vestibular, visual or musculoskeletal injuries or disease that limit the execution of the exercise and assessment protocols;
- No hypertension, cardiovascular, or respiratory disease.
You may not qualify if:
- Body mass index greater than 30 kg/m².
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Karine Josibel Velasques Stoelben
Uruguaiana, Rio Grande do Sul, 97502772, Brazil
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Felipe P Carpes, PhD
Universidade Federal do Pampa
- STUDY CHAIR
Marco A Vaz, PhD
Federal University of Rio Grande do Sul
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Masking Details
- The statistical analyzer will be masking for the time factor.
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
February 13, 2020
First Posted
February 18, 2020
Study Start
February 20, 2020
Primary Completion
October 5, 2021
Study Completion
March 30, 2022
Last Updated
November 5, 2020
Record last verified: 2020-11
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, CSR
- Time Frame
- The individual participant dataset will become available at a public repository up to six months after the first study publication
- Access Criteria
- A simple registration will grant access to study datasets. The website for these files is not defined at the time of registration.
The investigators intend to publish the results in an open-access journal, indexed at the Directory of Open Access Journals, with the copyrights transferred to the authors. Details regarding the study's design and statistical plan can be obtained consulting the trial's protocol. Data on other outcomes could be requested contacting the PI.