Efficacy of Postural Reeducation in Elite Gymnasts With Back Pain

November 2, 2022 updated by: Juan Martínez Fuentes, Universidad Católica San Antonio de Murcia

Efficacy of Postural Reeducation in Elite Gymnasts With Back Pain. A Randomized Clinical Trial

Introduction: Low back pain is a musculoskeletal disorder that is associated with symptoms such as pain, limitation of joint range and postural problems in athletes. Methods: The study design is a randomized controlled clinical trial with a minimum of 35 elite gymnasts with back pain. Two postural treatments will be implemented, Mezieres Method and Isostretching to verify if there is improvement of back pain in gymnasts and to compare both procedures. Discussion: This trial could generate a greater understanding of the importance of posture related to low back pain and its possible treatments.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

A randomized controlled clinical trial with two groups (intervention and placebo) will be implemented. The intervention group will have the Mezieres technique as postural treatment while the placebo group will follow a total of 6 isostretching positions.

In total, the two treatments with 30 minutes and duration or with a frequency of 2 weekly sessions will be implemented for a period of 12 weeks. All treatments will be performed by the same certified therapist and with a minimum of 5 years of experience in postural treatments. The measurements will be made immediately after the first session, in 2 weeks, 6 weeks and in the last week of intervention by a blind researcher who did not participate in the treatments, but with experience in this field.

Study Type

Interventional

Enrollment (Actual)

30

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

      • Murcia, Spain, 30107
        • Universidad Católica de Murcia

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

15 years to 30 years (ADULT, CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Elite gymnastic athletes with low back pain
  • Active participation in the national competition
  • Practice at least three times a week for 60 minutes
  • Minimum training time of 7 hours a week

Exclusion Criteria:

  • Gymnast whom suffer from chronic disease or acute musculoskeletal injury
  • Herniated disc
  • Spondylolisthesis

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: PARALLEL
  • Masking: TRIPLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Mezieres Group
This intervention includes a total of three postures of the Mézières therapy. Specifically, the postures maintained for 12 weeks consist of: supine dancer; in supine position with the upper extremities abducted 120 °; and dancer in a sitting position.
Implementation of 12 weeks suitable postures of Mezieres method
ACTIVE_COMPARATOR: Isostretching Group
This study aims to follow a total of 6 isostretching postures, the most similar to the Mezieres method. In each of the isostretching positions, if it is symmetric, 3, 6 or 9 repetitions will be performed and if it is asymmetric, 2, 4, or 8 repetitions.
Implementation of 12 weeks suitable postures of Mezieres method

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Back status
Time Frame: 12 weeks
Measured with Oswestry questionaire. It consists of 10 categories. Each category consists of 6 items scored from 0 to 5 with the first statement scoring 0 until the last statement scoring 5.
12 weeks
Back disability
Time Frame: 12 weeks
Measured with Roland Morris Questionaire wich consist in 24 points of back disability actual phrases
12 weeks
Range of motion
Time Frame: 12 weeks
Measured with Baiobit software
12 weeks
Pain intensity
Time Frame: 12 weeks
Measured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10
12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Subjetive tension perception
Time Frame: 12 weeks
Measured with Borg Scale, which include a rating of 6 perceiving "no exertion at all" to 20 perceiving a "maximal exertion" of effort.
12 weeks
Spinal curvature evaluation
Time Frame: 12 weeks
Measured with Spinal Mouse Software
12 weeks
Stiffness test
Time Frame: 12 weeks
Measured with Baiobit software
12 weeks
Posture stability
Time Frame: 12 weeks
Measured with stabilometry with a duration of 50 seconds with Lizard posturometric and stabilometric platform
12 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Juan Martínez Fuentes, Universidad Católica San Antonio de Murcia

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 (ACTUAL)

May 14, 2022

Primary Completion (ACTUAL)

June 16, 2022

Study Completion (ACTUAL)

July 30, 2022

Study Registration Dates

First Submitted

November 19, 2021

First Submitted That Met QC Criteria

December 2, 2021

First Posted (ACTUAL)

December 8, 2021

Study Record Updates

Last Update Posted (ACTUAL)

November 3, 2022

Last Update Submitted That Met QC Criteria

November 2, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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