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Core Endurance Versus Segmental Stabilization Exercise in Recreational Athletes With Low Back Pain

17 août 2026 mis à jour par: Doç.Dr.Ömer Şevgin, Uskudar University

Comparison of the Effects of Core Endurance Exercises and Segmental Stabilization Exercises on Low Back Pain and Core Endurance in Recreational Athletes With Non-Specific Low Back Pain: A Randomized Trial

Low back pain is a common musculoskeletal complaint among athletes, and most cases are classified as non-specific low back pain, in which no clear anatomical or pathological source of pain can be identified. Recreational athletes, who exercise regularly for health and fitness rather than for competition, often have less structured training planning and technical supervision than professional athletes, which may increase their susceptibility to musculoskeletal complaints. Core stability has become an important consideration in the prevention and management of low back pain. The core region includes the abdominal muscles, paraspinal muscles, diaphragm, and pelvic floor muscles, and plays an important role in maintaining spinal stability. Reduced activation and endurance of these muscles may increase the load on the lumbar spine and contribute to the development of low back pain. This randomized trial compares two exercise approaches in recreational athletes with non-specific low back pain: a core endurance exercise program and a segmental stabilization exercise program targeting the transversus abdominis and lumbar multifidus. Participants are randomly assigned to one of the two programs, both delivered three days per week for six weeks under physiotherapist supervision. Pain and functional status, dynamic balance, and core muscle endurance are assessed before the program and at the end of the six-week program.

Aperçu de l'étude

Description détaillée

Design and setting This is a two-arm, parallel-group randomized trial conducted at a sports club facility.

Institutional permission for the study site has been obtained. Participants Recreational athletes who have recently begun regular physical activity and who report non-specific low back pain are enrolled. Participants provide written informed consent after receiving detailed information about the purpose of the study, the tests to be performed, and the exercise protocol. Sampling and randomization Convenience sampling is used to identify eligible participants, followed by simple random allocation to one of the two exercise groups: the core endurance exercise group or the segmental stabilization exercise group. Allocation is 1:1. Interventions Both exercise programs are delivered three days per week for six weeks. Segmental stabilization group: exercises target the transversus abdominis and lumbar multifidus and comprise stabilization exercises in the quadruped position, transversus abdominis activation exercises in the supine position with the knees flexed, lumbar multifidus activation exercises in the prone position, and standing postural control exercises involving co-activation of the transversus abdominis and lumbar multifidus.

Core endurance group: exercises are performed under the supervision of a certified physiotherapist and comprise the front plank, the side plank, and the superman plank.

Each exercise consists of 20 repetitions with a 15-second isometric hold per repetition.

The set is repeated twice, with a 3-minute rest between sets. In the front plank the participant is supported on the forearms and toes, with the shoulders aligned over the elbows and the trunk and lower limbs maintained in a straight line, producing simultaneous activation of the abdominal and paraspinal muscles. In the side plank the participant is supported on one forearm with the body held in a straight line, the shoulder aligned with the elbow and the pelvis lifted from the floor, targeting the oblique muscles. In the superman plank the participant lies prone with the arms extended overhead and simultaneously lifts the upper and lower limbs from the floor, producing trunk extension and targeting the lumbar extensor muscles. Outcome assessment Assessments are performed at baseline (week 0) and at the end of the six-week program (week 6). Demographic information including age, sex, and sports history is recorded.

Functional status and pain are assessed with the Micheli Functional Scale, dynamic balance with the Star Excursion Balance Test, and core muscle endurance with clinical endurance tests. Variables The independent variable is the type of exercise program (core endurance exercises versus segmental stabilization exercises). The dependent variables are pain level, core muscle endurance, and dynamic balance performance. Statistical analysis Normality of distribution is assessed with histogram curves and the Shapiro-Wilk test, and homogeneity of variance with the Levene test. Parametric or non-parametric tests are selected accordingly. Analyses are performed with IBM SPSS Statistics 20. Independent samples t-tests are used to compare demographic characteristics between groups. Multivariate analysis of variance is used to evaluate between-group and within-group changes, with time (baseline and post-intervention measurements) as the within-subject factor and group as the between-subject factor. Where a statistically significant difference is found, post-hoc analyses are performed with the Tukey test. Change scores between groups are also compared with independent samples t-tests.

Type d'étude

Interventionnel

Inscription (Estimé)

60

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.

Coordonnées de l'étude

Lieux d'étude

      • Istanbul, Turquie (Türkiye)
        • Recrutement
        • Fitness club gym
        • Contact:
          • Armita Chitsaz
          • Numéro de téléphone: +905456052365

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:

  • Aged 18 years or older
  • Recreational athlete who has recently begun regular physical activity
  • Diagnosis of non-specific low back pain confirmed by an orthopaedic specialist
  • Two or more episodes of low back pain within the past year
  • Not participating in any other treatment program during the study period

Exclusion Criteria:

  • Radicular (nerve root) signs
  • Underlying systemic or visceral disease
  • Diagnosis of ankylosing spondylitis
  • Spinal pathology such as spondylolysis or spondylolisthesis
  • Previous lumbar spine surgery
  • History of vestibular dysfunction
  • Lower extremity injury within the past month
  • History of traumatic concussion within the past three months

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: Core endurance exercise
Participants perform a core endurance exercise program consisting of the front plank, the side plank, and the superman plank, three days per week for six weeks under physiotherapist supervision. Each exercise consists of 20 repetitions with a 15-second isometric hold, repeated for two sets with a 3-minute rest between sets.

Supervised isometric core endurance training comprising the front plank, side plank, and superman plank.

Each exercise: 20 repetitions of a 15-second isometric hold, two sets, 3-minute rest between sets. Three sessions per week for six weeks.

Supervised motor-control training targeting the transversus abdominis and lumbar multifidus, comprising quadruped stabilization, supine transversus abdominis activation with knees flexed, prone lumbar multifidus activation, and standing postural control with co-activation of both muscles. Three sessions per week for six weeks.
Comparateur actif: Segmental stabilization exercise
Participants perform a segmental stabilization exercise program targeting the transversus abdominis and lumbar multifidus, three days per week for six weeks under physiotherapist supervision. The program comprises quadruped stabilization exercises, supine transversus abdominis activation with the knees flexed, prone lumbar multifidus activation, and standing postural control exercises involving co-activation of both muscles.

Supervised isometric core endurance training comprising the front plank, side plank, and superman plank.

Each exercise: 20 repetitions of a 15-second isometric hold, two sets, 3-minute rest between sets. Three sessions per week for six weeks.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in low back pain and functional status (Micheli Functional Scale)
Délai: Baseline (week 0) and at the end of the six-week exercise program (week 6)
The Micheli Functional Scale is a five-item scale developed to assess low back pain related functional impairment and pain related changes in performance in athletes. It comprises one symptom question, three activity questions (extension, flexion, and jumping), and a visual analogue scale section. The symptom question is scored from 0 to 5; the activity questions are scored from 0 to 4 for extension, from 0 to 3 for flexion, and from 0 to 3 for jumping. The visual analogue scale section provides a 10-point assessment on a 10 cm line. The total score is calculated out of 25 and multiplied by 4 to produce a standardized score from 0 to 100. Lower scores indicate better functional status and higher scores indicate greater functional impairment.
Baseline (week 0) and at the end of the six-week exercise program (week 6)

Collaborateurs et enquêteurs

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

Parrainer

Les enquêteurs

  • Chaise d'étude: Armita Chitsaz, Uskudar University

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'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)

15 août 2026

Achèvement primaire (Estimé)

1 décembre 2026

Achèvement de l'étude (Estimé)

30 décembre 2026

Dates d'inscription aux études

Première soumission

7 août 2026

Première soumission répondant aux critères de contrôle qualité

7 août 2026

Première publication (Réel)

12 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

18 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

17 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Mots clés

Autres numéros d'identification d'étude

  • Uskudar27
  • Uskudar University (Autre identifiant: Non-Interventional Research Ethics Committee)

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 made publicly available. De-identified data supporting the findings may be made available from the corresponding author on reasonable request, subject to institutional approval.

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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