- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05149703
Efficacy of Postural Reeducation in Elite Gymnasts With Back Pain
Efficacy of Postural Reeducation in Elite Gymnasts With Back Pain. A Randomized Clinical Trial
Study Overview
Status
Conditions
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Murcia, Spain, 30107
- Universidad Católica de Murcia
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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.
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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
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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
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12 weeks
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Range of motion
Time Frame: 12 weeks
|
Measured with Baiobit software
|
12 weeks
|
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.
|
12 weeks
|
Spinal curvature evaluation
Time Frame: 12 weeks
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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
Investigators
- Principal Investigator: Juan Martínez Fuentes, Universidad Católica San Antonio de Murcia
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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