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Effect of the Suboccipital Inhibition Technique on Balance Changes

25 de junho de 2026 atualizado por: Natália Maria Oliveira Campelo, Escola Superior de Tecnologia da Saúde do Porto

Postural balance is an essential capacity for functional autonomy and the performance of activities of daily living, relying on the continuous integration of visual, vestibular, and somatosensory information. Within this system, the upper cervical region plays a particularly important role, as it contributes to the orientation of the head in space and to the coordination between the head, eyes, and trunk. Due to their deep location between the occiput, atlas, and axis, the suboccipital muscles have a high proprioceptive significance and are frequently associated with cervical position control and sensorimotor regulation.

Changes in muscle tension, stiffness, or dysfunction in this region may alter the quality of afferent information transmitted to the central nervous system, potentially interfering with postural stability, head position awareness, body sway, and center of pressure control. In this context, the suboccipital inhibition technique is used in osteopathic practice as a manual intervention aimed at reducing myofascial tension, promoting relaxation of the upper cervical musculature, and potentially normalizing proprioceptive input.

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Ainda não está recrutando

Condições

Descrição detalhada

Postural balance is a fundamental component of human motor function and is essential for maintaining functional autonomy and performing activities of daily living. It relies on the continuous and dynamic integration of sensory inputs from the visual, vestibular, and somatosensory systems, which are processed by the central nervous system to generate appropriate motor responses. These responses allow the body to maintain the center of mass within the base of support through constant postural adjustments.

Within this complex sensorimotor system, the upper cervical region plays a critical role in postural control. This region is responsible for the precise orientation of the head in space and contributes significantly to the coordination between the head, eyes, and trunk. The suboccipital muscles-namely the rectus capitis posterior major and minor, and the obliquus capitis superior and inferior-are deeply located between the occiput, atlas, and axis, and are characterized by a high density of muscle spindles. This anatomical feature suggests a strong proprioceptive function, making these muscles key contributors to cervical position sense and sensorimotor regulation.

In addition to their proprioceptive role, the suboccipital muscles are anatomically and functionally connected to the dura mater through the myodural bridge. This structure is thought to play a role in both mechanical and sensory integration, linking muscular activity with the central nervous system. Furthermore, the upper cervical region contains joint mechanoreceptors that provide additional afferent input, contributing to reflex mechanisms such as the cervico-ocular, cervico-collic, and tonic neck reflexes, which are essential for maintaining postural stability and gaze control.

Alterations in muscle tone, increased stiffness, or dysfunction in the suboccipital region may disrupt the quality of afferent information transmitted to the central nervous system. Such disturbances can impair proprioceptive accuracy and interfere with postural control mechanisms, potentially leading to increased body sway, altered head positioning, and changes in center of pressure (CoP) behavior. Since CoP displacement reflects the neuromuscular strategies used to maintain balance, it serves as an objective measure for assessing postural stability.

The suboccipital inhibition technique is commonly used in osteopathic practice as a manual intervention aimed at reducing myofascial tension in the upper cervical region. By promoting muscle relaxation and potentially restoring normal proprioceptive input, this technique may contribute to the optimization of postural control mechanisms. Previous studies have demonstrated its effects on cervical mobility, pain reduction, and flexibility; however, evidence regarding its immediate impact on postural balance remains limited and inconclusive.

Given the theoretical and neurophysiological rationale supporting the role of the suboccipital region in postural regulation, further investigation is warranted. The present study aims to evaluate the immediate effects of the suboccipital inhibition technique on postural balance in healthy young adults, using objective measures derived from center of pressure analysis, specifically Mean CoP and Mean Velocity.

Tipo de estudo

Intervencional

Inscrição (Estimado)

74

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

  • Nome: Natalia MO Campelo
  • Número de telefone: +351222061000
  • E-mail: nmc@ess.ipp.pt

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

Sim

Descrição

Inclusion Criteria:

  • Healthy individuals (defined by the absence of the exclusion criteria listed below)
  • Aged between 18 and 35 years
  • Signed informed consent form

Exclusion Criteria:

  • Recent history of falls
  • History of spinal or foot surgery
  • Cervical fractures
  • Known postural instability
  • Suspected neurovascular compromise
  • Neurological deficits
  • Neurological or vestibular disorders
  • Use of medication or substances that may affect the nervous system
  • Osteopathy students from the 2nd, 3rd, and 4th academic years

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: Dobro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Experimental Group
The intervention group received the suboccipital muscle inhibition technique, in which the investigator applied a sustained pressure to the patient's suboccipital muscle region for 4 minutes.

For the application of the suboccipital inhibition technique, the participant was positioned in the supine position on an osteopathic table, with the upper and lower limbs extended, the cervical spine in a neutral position, and the eyes closed. The therapist was seated at the head of the table, with the feet firmly supported on the floor.

The technique was performed by placing the 2nd, 3rd, and 4th fingers of both hands in the region between the occiput and the atlas, at the level of the suboccipital musculature, with the metacarpophalangeal joints flexed at approximately 90°. After correct positioning, a gentle and sustained pressure was applied, combined with a slight cephalic traction, in order to promote relaxation of the suboccipital muscles. The technique was applied for 4 minutes.

Comparador de Placebo: Control Group
In the control group, a clavicular palpation technique was performed, without any therapeutic intent.

For the placebo technique, the participant remained in the supine position on the osteopathic table, with the upper and lower limbs extended, the cervical spine in a neutral position, and the eyes closed. The therapist placed the hands in the clavicular region, performing only passive manual contact, without applying pressure, mobilisation, or any therapeutic intent.

This technique was used to reproduce the manual contact present in the intervention, without producing specific therapeutic effects. The application also lasted 4 minutes.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Mean Center of Pressure (Mean CoP) Displacement Assessed Using a Force Platform
Prazo: Immediately after the intervention
Mean center of pressure displacement will be assessed using a force platform during [static balance task]. Lower COP displacement indicates better postural stability.assessment period.
Immediately after the intervention
Mean Standing Velocity Assessed During Quiet Standing
Prazo: Immediately after the intervention
Mean velocity during quiet standing will be assessed using [measurement device/system name]. Participants will stand in an upright position while postural sway is recorded. Mean velocity will be calculated as the average velocity of the center of pressure (COP) displacement over the assessment period and expressed in [units, e.g., mm/s]. Lower values indicate reduced postural sway and better postural stability.
Immediately after the intervention

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Natalia MO Campelo, Escola Superior de Saúde do Porto

Publicações e links úteis

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Publicações Gerais

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 (Estimado)

1 de julho de 2026

Conclusão Primária (Estimado)

1 de setembro de 2026

Conclusão do estudo (Estimado)

1 de setembro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

22 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

22 de junho de 2026

Primeira postagem (Real)

26 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

25 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

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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