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Effects of Mezieres Method on Muscle Imbalance, Body Awareness and Postural Alignment in Athletes With Lower Back Pain. (MEZ-LBP)

20 mai 2026 mis à jour par: Wayna Maqsood, Green International University
The current study is a randomized controlled trial aims to compare the effectiveness of the Mezieres Method combined with core stabilization versus routine physiotherapy involving core stabilization on muscle imbalance, body awareness, and postural alignment in athletes with lower back pain. Eligible participants will be randomly allocated into two groups: an experimental group receiving the Mezieres Method plus core stabilization exercises and a control group receiving routine physiotherapy treatment involving core stabilization alone. Outcomes related to muscle imbalance, body awareness, postural alignment, and pain/function will be assessed before and after the intervention period. The study seeks to determine whether the Mezieres Method combined with core stabilization provides additional benefits in athletes with lower back pain.

Aperçu de l'étude

Description détaillée

Low back pain (LBP) is the type of musculoskeletal problems affecting athletes in many sports, and it is approximately about 80% of them experience at least one episode during their career and many of them later develops long duration or recurrent pain that definitely impact performance, training routine and also day-today quality of life . Lower back pain is one of the most common musculoskeletal conditions worldwide, particularly among athletes because of repetitive strain, poor biomechanics, and muscle imbalances. In the world wide, studies estimate that nearly 60-80% of individuals experience low back pain at some point in their lives, with a point prevalence of about 7-12% in the total population and even higher rates reported in athletic populations due to intensive physical demands. In sports communities, the prevalence can range from 20% to 50%, depending on the type of sport, training intensity, and postural habits. Locally, in countries like Pakistan, the burden of low back pain is also significantly high, although underreported; hospital-based and regional studies suggest prevalence rates ranging from 30% to 70% among adults, with athletes and physically active individuals being at increased risk due to inadequate conditioning, poor posture, and lack of body awareness. These rising trends focused the importance of effective rehabilitation approaches such as the Mezieres method, which mostly focuses on correcting muscle imbalance, improving body awareness, and restore the good postural alignment. In early morning many athletes often complain more stiffness and they are type of more predisposed to LBP because of routine mechanical loading, postural strains, asymmetric movements and high demands on spinal flexibility and strength. Sports like gymnastics, soccer and dance place unusual stress on the lumbar region through repeated hyperextension, twisting and high-impact movements, which sort of increase the risk even more. These biomechanical stresses can lead to muscle imbalance, postural changes and sometimes impaired neuromuscular control, and all of this basically keep the pain going with functional limitation. The pathophysiology of LBP in athletes sometimes includes multifactorial origins including poor lumbopelvic stability, weak core muscles and asymmetrical tension in posterior muscular chains. This muscular imbalance can disrupt spinal alignment and even change the proprioceptive control so athletes start using compensatory movement patterns and recurrent injury kind of occurred again. Traditional physical therapy usually emphasis on strengthening the core, better flexibility and decrease pain with therapeutic exercises and manual therapy. Core stabilization exercises in especially have shown good efficacy on patients in improving spinal stability, posture and reducing LBP intensity. So the present study is purpose to compare effects of Mezieres Method combined with core stabilization exercises to routine physiotherapy (core stabilization exercises alone) on muscle imbalance, body awareness and postural alignment in athletes with lower back pain. And by doing so it seeks to determine whether integration of global postural re-education offers additional benefits over conventional therapeutic practices and whether difference between groups is clinically meaningful for athletes who receive these treatments.

Type d'étude

Interventionnel

Inscription (Réel)

36

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54000
        • Green International University

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Diagnosed with non-specific LBP lasting at least three months with following test (Straight Leg Raise Test, Slump Test, Schober's Test )
  • Athletes aged 18-35 years of either gender
  • Athletes should exhibit signs of postural imbalance or muscular chain dysfunction
  • Functional limitation related to posture or movement.
  • Patient undergoing physiotherapy intervention for musculoskeletal disorders.
  • Reduced trunk mobility, impaired postural alignment, or functional defects.

Exclusion Criteria:

  • History of spinal surgery, fracture, or structural deformity (e.g., scoliosis, spondylolisthesis).
  • Neurological or systemic disorders affecting balance or muscle control
  • Current use of medications that may effect musculoskeletal performance (e.g., corticosteroids, muscle relaxants)
  • Pregnancy or any contraindication to physical activity

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Mezieres method plus core stabilization
Participants in this arm will receive the Mezieres Method combined with core stabilization exercises. The intervention will focus on global postural stretching, correction of muscle chain imbalance, breathing control, body awareness training, and activation of deep core muscles to improve postural alignment and functional outcomes in athletes with lower back pain. Treatment sessions will be supervised by a physiotherapist and conducted according to the study protocol throughout the intervention period.
Participants in Group A was receive Mezières method therapy, focusing on progressive stretching and postural correction aimed at restoring muscle balance and improving awareness of body alignment. Sessions was target major posterior chain muscles, including the erector spinae, hamstrings, and gluteal muscles, using slow, sustained stretching techniques. Each Mezières session was last 30-35 minutes, followed by core stabilization exercises for 15-20 minutes, including plank variations, bridging exercises, and abdominal hollowing techniques to enhance trunk stability. Interventions was administered 3 times per week for 6 weeks by a trained physiotherapist.
Autres noms:
  • Group A intervention
Comparateur actif: Routine physiotherapy (core stabilization)
Participants in this arm will receive routine physiotherapy management consisting of conventional core stabilization exercises, lumbar strengthening, stretching exercises, and standard physiotherapy rehabilitation techniques commonly used for lower back pain in athletes. Sessions will be conducted with the same treatment frequency and duration as the experimental group.
Participants in Group B was perform the same core stabilization exercises as Group A, without Mezières intervention. Exercises was target deep abdominal muscles, multifidus, and pelvic stabilizers, purpose is to improve trunk stability and support postural alignment. Each session was last 20-25 minutes, conducted 3 times per week for 6 weeks, under supervision to ensure correct technique and progression.
Autres noms:
  • Group B intervention

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Muscle Imbalance
Délai: Baseline and after six weeks
Muscle imbalance refers to unequal strength or flexibility between opposing lumbar pelvic muscle groups. Muscle imbalance will be assessed using the NYPRC postural alignment and muscle imbalance assessment protocol. The NYPRC evaluates postural deviations and muscle imbalance patterns through observational assessment of body alignment in standing posture. Scores are assigned to different body segments, with lower scores indicating greater postural deviation and muscle imbalance and higher scores indicating better alignment.
Baseline and after six weeks
Postural Alignment
Délai: Baseline and after six weeks
Postural alignment refers to the biomechanical positioning of the spine and pelvis across sagittal, frontal, and transverse planes. The New York Posture Rating Chart (NYPRC) is used to evaluate postural alignment and stability by assessing different body segments. Interpretation: Scores are assigned based on alignment of body parts (head, shoulders, spine, pelvis, etc.) Higher total score = better posture and stability Lower score = poor posture or imbalance
Baseline and after six weeks

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Body Awareness
Délai: Baseline and after six weeks
Body awareness describes one's conscious perception and control of body position and movement. It was measured using the validated Body Awareness Questionnaire (BAQ). Higher scores reflect better proprioceptive integration. Improvements was supported by participants' subjective reports of enhanced comfort, control, and movement confidence during functional tasks.
Baseline and after six weeks
Pain Intensity
Délai: Baseline and after six weeks
Pain intensity represents the participant's subjective level of lower back discomfort. It was evaluated using the VAS, ranging from 0 to 10. A clinically meaningful change is defined as a reduction of two or more points, as supported by previous athletic rehabilitation trials.
Baseline and after six weeks

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 janvier 2025

Achèvement primaire (Réel)

5 mars 2026

Achèvement de l'étude (Réel)

10 mai 2026

Dates d'inscription aux études

Première soumission

14 mai 2026

Première soumission répondant aux critères de contrôle qualité

20 mai 2026

Première publication (Réel)

28 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

28 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

20 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

Individual participant data will not be publicly shared to maintain participant confidentiality and privacy. The study data are intended for academic and research purposes only and are subject to institutional ethical guidelines and consent limitations.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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