Mézières Therapy in the UCAM's Athletes With Low Back Pain

Sponsor
Universidad Católica San Antonio de Murcia (Other)
Overall Status
Completed
CT.gov ID
NCT03849053
Collaborator
(none)
139
2
17.6

Study Details

Study Description

Brief Summary

The purpose of this research study focuses on the re-harmonization of the kinetic chains and posture based on spinal muscular atrophy and global stretching while trying to test the effectiveness of Mézières therapy on sports subjects with low back pain.

Condition or Disease Intervention/Treatment Phase
  • Other: Mézières Therapy for Low back pain
N/A

Detailed Description

The experimental study was conducted on 139 young athletes of National Rhythmic Gymnastics of Murcia, UCAM Murcia CF and UCAM Murcia CB/EBA during a six months period in the city of Murcia. Precisely, the Mézières therapy was conducted in an experimental group of 69 athletes and in a control group with other 70 athletes with Low Back Pain. This study is developed through a cycle of global stretching decompensate interventions on the athletes with postural alterations and vertebral pain at 95% confidence level. The statistical analysis was handled by using the univariate general linear model with the support of SPSS statistics.

Study Design

Study Type:
Interventional
Actual Enrollment :
139 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Effectiveness of Mézières Therapy in the UCAM's Athletes With Low Back Pain
Actual Study Start Date :
Dec 1, 2016
Actual Primary Completion Date :
Jun 30, 2017
Actual Study Completion Date :
May 20, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mézières method

Other: Mézières Therapy for Low back pain
Spinal muscular global stretching

Active Comparator: Control Group

Other: Mézières Therapy for Low back pain
Spinal muscular global stretching

Outcome Measures

Primary Outcome Measures

  1. VAS (Visual Analogic Scale) [6 months]

    It consists in identifying the patient, on a 10 cm line, the point that best represents his pain, where 0 means no pain and 10 = worst possible pain.

  2. Sit and Reach flexibility test [6 months]

    Designed to test the flexibility of lower back and hamstring muscles and is important as a result of lumbar lordosis, forward pelvic tilt and lower back pain. The score is recorded to the nearest inch/cm or inch/cm as the distance reached by the hand. For women, the lowest value is ˂ -15 cm and the highest is ˃ +30 cm. For men instead, the lowest value is ˂ -20 cm and the highest is >+27 cm.

  3. Runtastic Performance Pedometer [6 months]

    - Runtastic PRO is an app aimed at recording fitness in many activities and sports. It captures all basic data: distance, average speed, speed between mile markers, altitude, pace, step between mile markers, duration, calories burned and route plotted on a map using Global Positioning System. The final result shows how many steps are made in the arc of the minute (st / 60sec).

Secondary Outcome Measures

  1. Roland-Morris Questionnaire (CRM) [6 months]

    Measures the physical disability of athletes and consists of 24 points of functional capacity of the back. The sense of progression is: the more serious the worse is the performance.

  2. Health status questionnaire (SF-12) [6 months]

    The questionnaire consists in 12 items of the 8 dimensions of the SF-36 (124) such as: physical function (2), social function (1), physical role (2), emotional role (2), mental health (2), vitality (1), body pain (1), general health (1). Meanwhile response options forms Likert-type scales that evaluate intensity or frequency are achieved.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • between 15 - 39 years

  • athletes with low back pain lasting more than 1 month

  • scoliosis

  • kyphosis

Exclusion Criteria:
  • presence of tumors or spinal metastases

  • vertebral fractures

  • osteoporosis

  • infection or inflammation in acute diseases with involvement of the central nervous system

  • herniated discs

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Universidad Católica San Antonio de Murcia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Orges Lena, Principal Investigator, Universidad Católica San Antonio de Murcia
ClinicalTrials.gov Identifier:
NCT03849053
Other Study ID Numbers:
  • BB8334280
First Posted:
Feb 21, 2019
Last Update Posted:
Mar 19, 2019
Last Verified:
Mar 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Orges Lena, Principal Investigator, Universidad Católica San Antonio de Murcia
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 19, 2019