Effect of the Pelvic Loin Musculature Training on the Dynamic Hip Stabilization

April 14, 2016 updated by: Camila Lazarin Gallina, Universidade Estadual do Centro-Oeste

Effect of the Pelvic Loin Musculature Training on the Dynamic Hip Stabilization: Random Clinical Trial

Introduction: The stability of the pelvis is of great importance in body balance as a whole, can be improved by training the pelvic muscles fillet (MLP), which is characterized by low intensity isometric synchronous and the deep muscles of the trunk. This study aims to determine the effect of a stability program target, with the training of the MLP region on pelvic stability.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study aims to determine the effect of a stability program target, with the training of the MLP region on pelvic stability. Materials and Methods: We recruited 20 volunteers of both sexes were randomly divided into control group (CG) and training group (TG). The evaluations were performed before and after training the MLP. The training was held four isometrics series with a time of 30 seconds with 30 seconds rest in between reps during 10 sessions distributed twice weekly.

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 35 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • considered individuals of both sexes, aged 18 and 35
  • absence of low back pain
  • lack of musculoskeletal dysfunction in the lower limbs
  • have never participated in any stabilization training program of the MLP region
  • agree to the Terms Informed consent form (ICF) and the sign voluntarily.

Exclusion Criteria:

  • the study of abandonment by a participant
  • the disagreement with the terms of IC and its not signing
  • the volunteer does not understand the implementation of dynamic hip stabilization test
  • present cramps or pain during the test and / or training
  • historical column in injury, knee and / or ankle.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Group control
It does not perform any kind of guided exercise.
Experimental: Core Training Group
The training was distributed in four positions defined ventral plank, side plank left, right side board and bridge semiflexion knees, respectively. With time isometric contraction of 30 seconds repeated four times with rest 30 seconds between repetitions. During 10 sessions distributed twice weekly.
Performs oriented exercise segmental stabilization lumbar-pelvic.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Values of pelvic tilts , left and right expressed in degrees ( ° ) , the control group (CG ) and training group (TG ) .
Time Frame: 5 weeks
5 weeks
Values of unilateral pelvic tilts between the control group (CG) and training group (TG ) after training.
Time Frame: 5 weeks
5 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Camila Gallina, Universidade Estadual do Centro-Oeste

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2014

Primary Completion (Actual)

October 1, 2014

Study Completion (Actual)

December 1, 2014

Study Registration Dates

First Submitted

March 11, 2016

First Submitted That Met QC Criteria

April 14, 2016

First Posted (Estimate)

April 15, 2016

Study Record Updates

Last Update Posted (Estimate)

April 15, 2016

Last Update Submitted That Met QC Criteria

April 14, 2016

Last Verified

April 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • CG 001

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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