Pilates, Postural Global Reeducation and Ball Exercises

August 5, 2014 updated by: Cintia Domingues de Freitas, University of Sao Paulo

Comparative Study of Strenght, Endurance, Flexibility of Muscle Trunk Between the Techniques: Global Postural Reeducation , Pilates and Segmented Dynamic Exercises.

The purpose of this study is to evaluate and compare the effects of three Exercise Movement Techniques Global Postural Reeducation(RPG), Pilates method and Segmented Dynamic Exercises (SDE) regarding muscular strength and endurance of the trunk, spine mobility and flexibility of the posterior muscle chain.

Study Overview

Study Type

Interventional

Enrollment (Actual)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • São Paulo, Brazil
        • Faculdade de Medicina da Universidade de Sao Paulo

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 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Men and women
  • Healthy young adults who do not practice regular exercise
  • The individuals could not have prior experience with the techniques covered in this study
  • They could not report a history of pain,disease, neurological or orthopedic surgeries in column , upper or lower limbs, joint laxity, nor have history of injury and hamstring muscles in the lower limbs, neurological disorders, obesity, rheumatic disease, labyrinthitis, deformities of the lower limbs and spine
  • Individuals could not make use of drugs that affected his balance and muscle strength
  • To be framed the individual should also have restricted movement in the test distance of the third finger to the ground

Exclusion Criteria:

  • Individuals with excessive absences (more than 20% of sessions) or those who missed and could not reset the session in the same week were excluded -Individuals who needed to undergo some surgery or any medical treatment during the duration of the study, or those who give up without completing the minimum time of the intervention

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Factorial Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pilates Group
The individuals were treated with Mat Pilates Method.
The exercises were applied once a week during eight weeks.
Experimental: Segmented Dynamic Exercises Group
The individual were treated with ball exercises.
The exercises were applied once a week during eight weeks. once a week for eight weeks.
Experimental: Global Postural Reeducation Group
The individuals were treated with postures of Souchard Method.
The exercises were applied once a week during eight weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Abdominal Muscle Endurance: Crunch test (repetitions per minute)
Time Frame: Baseline and week eight
Control Group: Baseline 30,86 Week eight 31,24 SDE Group: Baseline 25,06 Week eight 32,00 Pilates Group: Baseline 25,29 Week eight 34,14 RPG Group: Baseline 30,61 Week eight 36,17
Baseline and week eight
Extensors Muscle Endurance:Sorenson test (seconds)
Time Frame: Baseline and week eight
Control Group: Baseline 69,43 Week eight 69,67 SDE Group: Baseline 72,65 Week eight 112,76 Pilates Group: Baseline 73,67 Week eight 74,43 RPG Group: Baseline 77,39 Week eight 119,48
Baseline and week eight
Toe-touch test right/left
Time Frame: Baseline and week eight
Control Group: Baseline 14,61/14,87 Week eight 14,89/14,91 SDE Group: Baseline 12,95/13,2 Week eight 10,12/10,32 Pilates Group: Baseline 13,81/13,93 Week eight 11,90/12,01 RPG Group : Baseline 17,63/18,15 Week eight: 9,11/9,22
Baseline and week eight
Strength of trunk muscles:Peak Torque(Newton metre Nm) flexors and extensor muscles of spine measured in the isokinetic dynamometer BIODEX
Time Frame: Baseline and week eight

Extension Control Group Baseline 206,1 week eight 236,9 SDE Group Baseline 213,5 week eight 239,3 Pilates Group Baseline 228,5 week eight 243,8 RPG Group Baseline 242,5 week eight 280,3

Flexion Control Group Baseline 114,3 week eight 117,7 SDE Group Baseline 113,2 week eight 121,2 Pilates Group Baseline 109,3 week eight 118,5 RPG Group Baseline 127,2 week eight 138,1

Baseline and week eight
Strength of trunk muscles:Muscle Work (Joules) of flexors and extensor muscles of spine measured in the isokinetic dynamometer BIODEX
Time Frame: Baseline and week eight

Extension Control Group Baseline 847,9 week eight 958,6 SDE Group Baseline 893,5 week eight 985,4 Pilates Group Baseline 982,1 week eight 973,0 RPG Group Baseline 1053,1 week eight 1233,0

Flexion

Control Group Baseline 455,8 week eight 499,8 SDE Group Baseline 492,0 week eight 491,2 Pilates Group Baseline 472,0 week eight 498,9 RPG Group Baseline 558,7 week eight 581,9

Baseline and week eight

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Cintia de Freitas, student, FMUSP

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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

October 1, 2010

Primary Completion (Actual)

November 1, 2010

Study Completion (Actual)

December 1, 2012

Study Registration Dates

First Submitted

August 1, 2014

First Submitted That Met QC Criteria

August 5, 2014

First Posted (Estimate)

August 7, 2014

Study Record Updates

Last Update Posted (Estimate)

August 7, 2014

Last Update Submitted That Met QC Criteria

August 5, 2014

Last Verified

August 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • U1111-1159-8500

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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