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Clinical Trials/NCT04273971
NCT04273971UnknownNot Applicable

Acute Effect of Plyometric Exercises on Musculotendinous Properties of Quadriceps and Biceps Femoral

Universidade Federal de Santa Maria1 site in 1 country30 target enrollmentStarted: February 20, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
30
Locations
1
Primary Endpoint
Change from baseline of echo intensity of quadriceps and biceps femoral muscles

Study Overview

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.

Detailed Description

This is a single-arm clinical trial aiming to determine the acute effect of one session of plyometric exercises on quadriceps and biceps femoral musculotendinous properties in healthy individuals.

The sample size was determined using G*Power software considering the application of ANOVA: Repeated measures, between factors, 90% power, alpha 0.05. Data from muscle echo intensity of the rectus femoral by Muddle et al. (2019) were considered for this calculation, with an effect size 0.44. A total of 30 individuals was required for this study.

The outcomes will include the muscle and tendon quality, and mechanical properties of the tendon. The assessments will be performed at three different moments: before exercise, immediately after, and 48 hours after exercise.

The data analysis will be performed per protocol. Generalized estimating equations will be used to identify the effects of time followed by Bonferroni posthoc. When effects are found, effect sizes will be estimated. Missing data will be estimated by statistical analysis.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Masking Description

The statistical analyzer will be masking for the time factor.

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •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.

Exclusion Criteria

  • •Body mass index greater than 30 kg/m².

Arms & Interventions

Plyometric exercise

Experimental

Intervention: Plyometric exercises (Other)

Outcomes

Primary Outcomes

Change from baseline of echo intensity of quadriceps and biceps femoral muscles

Time Frame: Baseline, immediately after exercise and up to 48 hours exercise

Muscle echo intensity will be assessed for transversal and longitudinal ultrasonography images.

Change from baseline stiffness of patellar tendon

Time Frame: Baseline, immediately after exercise and up to 48 hours exercise

Patellar tendon stiffness during 5 seconds rampa contraction protocol. Patellar tendon stiffness will be estimate from force/deformation relationship of tendon.

Change from baseline young modulus of patellar tendon

Time Frame: Baseline, immediately after exercise and up to 48 hours exercise

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.

Secondary Outcomes

  • Change from baseline echo intensity of quadriceps and biceps femoral tendons(Baseline, immediately after exercise and up to 48 hours exercise)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Karine Josibel Velasques Stoelben

Principal Investigator

Universidade Federal do Pampa

Study Sites (1)

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