Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Sensorimotor Training With a Mobilized Balance Platform in Patients With Chronic Low Back Pain

16 maggio 2026 aggiornato da: Sefa Gümrük Aslan, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Effects of a Sensorimotor Training Protocol Using a Mobilized Balance Platform on Proprioceptive System, Movement Control, and Quality of Life in Patients With Chronic Low Back Pain

This randomized controlled study aims to investigate the effects of a sensorimotor training protocol using a mobilized balance platform device on proprioceptive system function, movement control, balance, physical performance, pain severity, and quality of life in patients with chronic low back pain. A total of 44 patients with chronic low back pain will be recruited from the outpatient clinic of Gaziler Physical Medicine and Rehabilitation Training and Research Hospital.

Participants will be randomly assigned to either a sensorimotor training group or a control group. The intervention group will receive sensorimotor training using the Huber 360 balance system, while the control group will perform a home exercise program including stretching, spinal mobility, lumbopelvic control, and balance exercises.

Pain severity, proprioception, functional status, balance, physical performance, and quality of life will be assessed before and after treatment by an assessor blinded to group allocation.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

44

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

  • Turchia (Türkiye)
      • Ankara, Turchia (Türkiye)
        • Reclutamento
        • Ankara Gaziler physical therapy and rehabilitation hospital
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Individuals aged between 18 and 55 years
  • Presence of chronic low back pain lasting at least 3 months
  • Pain intensity score of 3 or higher on the Visual Analog Scale (VAS)
  • Individuals with sufficient cognitive ability to understand and follow study procedures
  • Willingness to participate voluntarily in the study

Exclusion Criteria:

  • Participation in a similar training program within the last 12 months
  • History of lower extremity or spinal surgery
  • Presence of non-mechanical low back pain, inflammatory disease, or tumor
  • Uncontrolled hypertension or cardiac disease
  • History of malignancy
  • Presence of radicular symptoms associated with low back pain
  • Progressive neurological deficits
  • Neurogenic claudication

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: Home Exercise Program
Participants in this group will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises. The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
Comportamentale: Home Exercise Program
Participants will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises. The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
Sperimentale: Huber 360 Sensorimotor Training
Participants in this group will receive a sensorimotor training protocol using the Huber 360 balance system. The intervention will include progressive rotational and oscillatory exercises aimed at improving proprioception, balance, neuromuscular control, and movement control. Sessions will be performed for 30 minutes, twice weekly for 5 weeks.
Comportamentale: Home Exercise Program
Participants will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises. The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
Dispositivo: Huber 360 Sensorimotor Training
Participants will receive sensorimotor training using the Huber 360 balance system. The protocol will include progressive rotational and oscillatory exercises designed to improve proprioception, balance, neuromuscular control, and movement control in patients with chronic low back pain. Sessions will be performed for 30 minutes, twice weekly for 5 weeks.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Lumbar Proprioception Assessment
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
Lumbar proprioception will be assessed using lumbar repositioning tests at 60 degrees flexion and 15 degrees extension. Participants will be asked to reproduce target lumbar positions, and the angular repositioning error will be recorded. Lower repositioning error values indicate better lumbar proprioceptive accuracy.
Before treatment and immediately after completion of the 5-week intervention program

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Pain Severity Assessed by Visual Analog Scale
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
Pain intensity will be assessed using a 10-cm Visual Analog Scale (VAS). Scores range from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain severity.
Before treatment and immediately after completion of the 5-week intervention program
Functional Status Assessed by Oswestry Disability Index
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
Functional disability related to low back pain will be assessed using the Oswestry Disability Index (ODI). Higher scores indicate greater disability.
Before treatment and immediately after completion of the 5-week intervention program
Balance and Limits of Stability Assessed by Huber 360
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
Static balance, dynamic balance, and limits of stability will be assessed using the Huber 360 balance system. Better balance performance and improved stability limits indicate better postural control.
Before treatment and immediately after completion of the 5-week intervention program
Lumbar Flexion Range of Motion
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
Physical performance will be assessed using a Physical Performance Test Battery including lumbar flexion range of motion, 50-step walking test, 5-minute walking test, five-repetition sit-to-stand test, ten-repetition trunk flexion test, and forward reaching with weight.
Before treatment and immediately after completion of the 5-week intervention program
Quality of Life Assessed by Short Form-36
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
Quality of life will be assessed using the Short Form-36 (SF-36). Higher scores indicate better health-related quality of life.
Before treatment and immediately after completion of the 5-week intervention program
50-Step Walking Test
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
he time required to complete the 50-step walking test will be recorded in seconds
Before treatment and immediately after completion of the 5-week intervention program
Five-Minute Walking Test
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
The time required to complete five sit-to-stand repetitions will be recorded in seconds.
Before treatment and immediately after completion of the 5-week intervention program
Ten-Repetition Trunk Flexion Test
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
The time required to complete ten trunk flexion repetitions will be recorded in seconds.
Before treatment and immediately after completion of the 5-week intervention program
Forward Reaching with Weight Test
Lasso di tempo: Before treatment and immediately after completion of the 5-week intervention program
Forward reaching distance while holding weight will be measured in centimeters.
Before treatment and immediately after completion of the 5-week intervention program

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

4 maggio 2026

Completamento primario (Stimato)

30 ottobre 2026

Completamento dello studio (Stimato)

30 novembre 2026

Date di iscrizione allo studio

Primo inviato

3 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

16 maggio 2026

Primo Inserito (Effettivo)

22 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

16 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • CLBP-MBP-2026

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Lombalgia

Prove cliniche su Home Exercise Program

Cerca prove simili

Sponsor e collaboratori

Condizioni mediche

Interventi farmacologici

CROs by country

CROs in Morocco

Condizioni

Malattie rare

Interventi farmacologici

Supplementi dietetici

Sponsor / Collaboratori

Sedi

Sottoscrivi