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

16 de maio de 2026 atualizado por: 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.

Visão geral do estudo

Status

Recrutamento

Condições

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Estimado)

44

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

  • Turquia (Türkiye)
      • Ankara, Turquia (Türkiye)
        • Recrutamento
        • Ankara Gaziler physical therapy and rehabilitation hospital
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: 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.
Comportamental: 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.
Experimental: 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.
Comportamental: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Lumbar Proprioception Assessment
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Pain Severity Assessed by Visual Analog Scale
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

4 de maio de 2026

Conclusão Primária (Estimado)

30 de outubro de 2026

Conclusão do estudo (Estimado)

30 de novembro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

3 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

16 de maio de 2026

Primeira postagem (Real)

22 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

22 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

16 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • CLBP-MBP-2026

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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