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Effects of Whole-Body Vibration and Cervical Stabilization With Core Stabilization in Young Adults With Non-Specific Low Back Pain

5 novembre 2026 mis à jour par: Çiçek Günday, Istinye University

Effects of Whole-Body Vibration and Cervical Stabilization Combined With Core Stabilization on Trunk Motor Control in Young Individuals With Non-Specific Low Back Pain

This study aims to investigate the immediate effects of three intervention approaches in young adults with nonspecific low back pain. Participants will be randomly assigned to one of three groups: core stabilization exercises, whole-body vibration combined with core stabilization exercises, or cervical stabilization combined with core stabilization exercises. Outcomes will be assessed before and immediately after the intervention. The study will evaluate trunk motor control, pain intensity, pressure pain threshold, trunk muscle endurance, and balance. The purpose is to compare the immediate effects of these approaches and determine whether adding whole-body vibration or cervical stabilization to core stabilization produces additional benefits.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

48

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

Sauvegarde des contacts de l'étude

  • Nom: Çiçek Günday Asst. Prof., Asst. Prof.
  • Numéro de téléphone: +905071888848

Lieux d'étude

    • Istanbul
      • Istanbul, Istanbul, Turquie (Türkiye)
        • Istinye University Physiotherapy and Rehabilitation Application and Research Center (ISUFIZYOTEM)
        • Contact:
          • Nurgül Elbaşı Elbaşı

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

18 ans à 30 ans (Adulte)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Age between 18 and 30 years.
  • Low back pain intensity of at least 3/10 on the Numeric Rating Scale.
  • Low back pain symptoms for at least 6 months.
  • Ability to understand and follow verbal instructions.
  • No major neurological deficit.
  • No physiotherapy for low back pain within the previous 6 weeks.

Exclusion Criteria:

  • Low back pain with a specific etiology identified by a physician.
  • Neurological, vestibular, rheumatological, or serious musculoskeletal disorders affecting balance or motor control.
  • Use of medications that may affect balance or have potential neurotoxic effects.
  • Degenerative diseases.
  • Indication for surgical intervention.
  • History of fracture or surgery within the previous 2 years.

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: Soins de soutien
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: Core Stabilization

Participants in this group will perform the standard core stabilization exercise program, including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The total intervention duration is approximately 20 minutes.

Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles.

Expérimental: Whole-Body Vibration + Core Stabilization

Participants in this group will receive 5 minutes of whole-body vibration before the core stabilization exercise program. The vibration platform will be set at 30 Hz with an amplitude of 2 mm, and participants will stand with the knees slightly flexed during the vibration. Immediately afterward, participants will perform the same core stabilization exercise program used in the core stabilization group. After completing the core stabilization exercises, an additional 5 minutes of whole-body vibration will be applied using the same parameters. The total intervention duration is approximately 30 minutes.

Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles.

Whole-body vibration will be applied using a vibration platform at a frequency of 30 Hz and an amplitude of 2 mm. Participants will stand on the platform with the knees slightly flexed for 5 minutes before the core stabilization exercise program and for an additional 5 minutes after the program.

Expérimental: Cervical Stabilization + Core Stabilization

Participants in this group will perform cervical stabilization exercises before the core stabilization exercise program. The cervical exercises will be performed in supine using a pressure biofeedback unit placed under the cervical spine. Participants will perform controlled craniocervical flexion, progressing the target pressure from 20 mmHg to 30 mmHg in 2 mmHg increments. The cervical stabilization exercises will be performed for approximately 5 minutes before the core stabilization program and repeated for an additional 5 minutes afterward. The total intervention duration is approximately 30 minutes.

Participants perform a core stabilization exercise program including the abdominal drawing-in maneuver, heel slide, single-leg march, single-leg extended heel tap, bridge, bridge pulse, dead bug, modified curl-up, and semi-plank. The program is designed to activate and control the deep trunk stabilizing muscles.

Participants will perform cervical stabilization exercises in the supine position using a pressure biofeedback unit placed under the cervical spine. Controlled craniocervical flexion will be performed with progressive target pressures from 20 mmHg to 30 mmHg in 2 mmHg increments. The exercises will be performed for approximately 5 minutes before the core stabilization program and repeated for an additional 5 minutes afterward.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Trunk motor control (supine), Pressure Biofeedback Unit
Délai: Baseline and immediately after the single intervention session

Deep abdominal muscle activation and lumbopelvic stability assessed with a pressure biofeedback unit in crook lying during the abdominal drawing-in maneuver, starting at 40 mmHg. The score is the absolute deviation from 40 mmHg (best of three trials); smaller values indicate better motor control.

Baseline and immediately after the single intervention session
Trunk motor control (prone; transversus abdominis activation), Pressure Biofeedback Unit
Délai: Baseline and immediately after the single intervention session

Activation of the transversus abdominis assessed in prone lying with the pressure biofeedback unit placed under the abdomen and inflated to 70 mmHg. Participants draw the abdominal wall in without moving the spine or pelvis. The score is the pressure reduction from 70 mmHg held steadily (best of three trials); larger reductions indicate better activation.

Baseline and immediately after the single intervention session

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Pain intensity, Numeric Pain Rating Scale (NPRS)
Délai: Baseline and immediately after the single intervention session

Self-reported low back pain intensity rated from 0 (no pain) to 10 (worst imaginable pain). Lower scores indicate less pain.

Baseline and immediately after the single intervention session
Pressure pain threshold, lumbar multifidus
Délai: Baseline and immediately after the single intervention session

Pressure pain threshold in kg/cm² measured with a pressure algometer 2 cm lateral to the L4 spinous process. The mean of three measurements is used. Higher values indicate lower pain sensitivity.

Baseline and immediately after the single intervention session
Pressure pain threshold, erector spinae
Délai: Baseline and immediately after the single intervention session

Pressure pain threshold in kg/cm² measured with a pressure algometer 3 cm lateral to the L3 spinous process. The mean of three measurements is used. Higher values indicate lower pain sensitivity.

Baseline and immediately after the single intervention session
Pressure pain threshold, thoracolumbar fascia
Délai: Baseline and immediately after the single intervention session

Pressure pain threshold in kg/cm² measured with a pressure algometer 5 cm lateral to the L3 level. The mean of three measurements is used. Higher values indicate lower pain sensitivity.

Baseline and immediately after the single intervention session
Y-Balance Test composite score, right leg
Délai: Baseline and immediately after the single intervention session

Maximum reach in the anterior, posteromedial and posterolateral directions while standing on the right leg, normalized to right lower limb length and expressed as a composite score (%). Higher scores indicate better dynamic balance.

Baseline and immediately after the single intervention session
Y-Balance Test composite score, left leg
Délai: Baseline and immediately after the single intervention session

Maximum reach in the anterior, posteromedial and posterolateral directions while standing on the left leg, normalized to left lower limb length and expressed as a composite score (%). Higher scores indicate better dynamic balance.

Baseline and immediately after the single intervention session
Trunk flexor endurance test
Délai: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the trunk flexor endurance test (McGill). Longer holding time indicates greater trunk flexor endurance.

Baseline and immediately after the single intervention session
Prone plank test
Délai: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the prone plank position. Longer holding time indicates greater trunk muscle endurance.

Baseline and immediately after the single intervention session
Right side bridge test
Délai: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the right side bridge test (McGill). Longer holding time indicates greater lateral trunk endurance.

Baseline and immediately after the single intervention session
Left side bridge test
Délai: Baseline and immediately after the single intervention session

Isometric holding time in seconds in the left side bridge test (McGill). Longer holding time indicates greater lateral trunk endurance.

Baseline and immediately after the single intervention session

Collaborateurs et enquêteurs

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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 (Estimé)

30 octobre 2026

Achèvement primaire (Estimé)

30 octobre 2027

Achèvement de l'étude (Estimé)

30 octobre 2027

Dates d'inscription aux études

Première soumission

21 octobre 2026

Première soumission répondant aux critères de contrôle qualité

5 novembre 2026

Première publication (Réel)

6 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

6 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

5 novembre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

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Description du régime IPD

Individual participant data will not be shared in order to protect the privacy and confidentiality of the participants.

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

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Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

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