Neuromuscular Training and Strengthening CORE in Volleyball Amateur Players 18 to 25 Years

I

Investigación en Hemofilia y Fisioterapia

Status

Completed

Conditions

Stability

Treatments

Other: Experimental
Other: Control

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT03866096
ENCORE

Details and patient eligibility

About

Introduction. The most popular injuries in volleyball are the ones who occur in knee joints, due the jumps and landings that happen through the game. For this reason there is a high index of loss of stability because of the dynamic valgus during the landing, a loss of balance and a decrease of power during the jumps. Objective. Evaluate the effectiveness of neuromuscular training in combination with strengthening of CORE in the improvement of knee joint stability, balance and power in vertical jump in volleyball players from 18 to 25 years old. Study design. Randomized, multicenter, single-blind clinical study with follow-up period. Methods. The study will be realized with an initial sample of 30 players, which in a random way, will be divided into two groups: experimental and control. It will be realized an initial evaluation where sociodemographic, anthropometric and clinical measures will be taken, and the study variables: knee joint stability (single leg squat test), balance (star excursion balance test) and vertical jump (sargent jump test). The intervention will last six weeks, with two sessions per week of approximately twenty minutes each. Expected results. The investigators expected to observe improvement in the stability in the knee joint, balance and power in the vertical jump in 18-25 years volleyball players that have received a neuromuscular training with strengthening of CORE.

Enrollment

30 patients

Sex

Female

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Volleyball players
  • Female
  • From 18 to 25 years
  • With more than one year of sports practice
  • Currently participate in amateur industry competitions

Exclusion criteria

  • Present a medical diagnosis of musculoskeletal injury at the time of beginning the study
  • Receive a physiotherapy treatment unrelated to the study
  • Have suffered neurological pathology in the last 6 months
  • Have some type of auditory or vestibular disorder
  • Not signed the informed consent.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Experimental
Experimental group
Description:
Each session will last 20 minutes, taking place during 2 days a week, in a period of 6 weeks. The intervention will be made prior to the training session. The subjects of the experimental group will receive an intervention through neuromuscular training and a CORE strengthening program
Treatment:
Other: Experimental
Control
Active Comparator group
Description:
Each session will last 20 minutes, taking place during 2 days a week, in a period of 6 weeks. The intervention will be made prior to the training session. The subjects of the experimental group will receive an intervention through neuromuscular training.
Treatment:
Other: Control

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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