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Plyometric and Eccentric Training in Improving the Strength, Stability and Ability of Women Soccer Players

NCT04255290 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2021-09-02

No results posted yet for this study

Summary

Introduction. The high rate of recurrence and clinical involvement of muscle injuries in lower limbs, makes the hamstring musculature a very important structure in the development of athletes. Excentric movements, where eccentric force and flexibility are fundamental, and the quadriceps-hamstrings contraction cycle are risk factors for hamstring muscle injury.

Aim. ascertain the effectiveness of plyometric and excéntric exercises in the improvement of hamstring strength.

Study design. Randomized, prospective, multicenter, single-blind clinical study with athletes.

Methods. This study will be carried out with a sample of 40 women, federated players from 18 to 30 years old. They will be randomized into two groups: experimental (plyometric work and eccentric exercises) and control (eccentric exercises). The intervention will last 6 weeks in which, before each training, they will carry out the intervention, for 20 minutes, 3 days a week. An inter-judges piloting will be carried out. We will analyze the normality of the sample with the Kolmogorov-smirnov test and for the inferential analysis, we will use the t-student test of paired data to observe the difference between each evaluation in each study group, and the repeated measures ANOVA to calculate the effect intra and intergroup. Using Cohen's formula we will calculate the size of the effect.

Expected results. The eccentric work along with the plyometrics improves strength in hamstrings, jumping and stability.

Conditions

  • Female Athlete

Interventions

OTHER

Leg Squat Lounge

The players assigned to the experimental group will receive an intervention through plyometric and eccentric hamstring exercises

OTHER

Control group

The subjects included in the control group will perform an eccentric work protocol

Sponsors & Collaborators

  • Investigación en Hemofilia y Fisioterapia

    lead NETWORK

Principal Investigators

  • Rubén Cuesta-Barriuso, PhD · Universidad Europea de Madrid

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-02-10
Primary Completion
2020-04-30
Completion
2020-05-10

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04255290 on ClinicalTrials.gov