- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05149703
Efficacy of Postural Reeducation in Elite Gymnasts With Back Pain
February 19, 2026 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.
Postural control is a key factor in disciplines with high biomechanical demands, such as rhythmic gymnastics.
In addition, the potential influence of occlusal splints on body posture has been discussed, although evidence remains inconclusive.
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 whether there is improvement in low back pain in gymnasts and to compare both procedures.
Postural variables will also allow exploratory analysis of factors potentially associated with postural regulation, including the possible influence of occlusal-byte use.
Discussion: This trial could generate a greater understanding of the importance of posture related to low back pain and its possible treatments.
It may also contribute to clarifying the relationship between postural therapeutic approaches and other factors influencing postural control.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
A randomized controlled clinical trial with two groups (intervention and placebo) will be implemented.
The intervention group will receive the Mezieres technique as postural treatment, while the placebo group will perform a total of six Isostretching positions.
Both interventions will consist of 30-minute sessions delivered twice weekly over a 12-week period.
All treatments will be administered by the same certified therapist with at least five years of experience in postural therapy.
Outcome measurements will be obtained immediately after the first session, and at 2, 6, and 12 weeks.
Assessments will be conducted by a blinded researcher who will not participate in the treatments and who has prior experience in postural evaluation.
Postural measurements will additionally permit exploratory analyses of factors potentially influencing postural regulation, including the possible impact of occlusal-byte use.
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
-
-
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Murcia, Spain, 30107
- Universidad Católica de Murcia
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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 (Child, Adult)
Accepts Healthy Volunteers
Yes
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 Assignment
- 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
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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
|
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Back disability
Time Frame: 12 weeks
|
Measured with Roland Morris Questionaire wich consist in 24 points of back disability actual phrases
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12 weeks
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Range of motion
Time Frame: 12 weeks
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Measured with Baiobit software
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12 weeks
|
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Pain intensity
Time Frame: 12 weeks
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Measured with Numeric Rating Scale wich consist in measure pain intensity with a score of 0-10
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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.
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12 weeks
|
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Spinal curvature evaluation
Time Frame: 12 weeks
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Measured with Spinal Mouse Software
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12 weeks
|
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Stiffness test
Time Frame: 12 weeks
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Measured with Baiobit software
|
12 weeks
|
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Posture stability
Time Frame: 12 weeks
|
Measured with stabilometry with a duration of 50 seconds with Lizard posturometric and stabilometric platform
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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)
February 23, 2026
Last Update Submitted That Met QC Criteria
February 19, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CE102105
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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