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- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT03029260
Effects of Nervous System Mobilization
Effect of Nervous System Mobilization on Heat, Cold and Mechanical Pain Thresholds and Lower Limb Flexibility
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
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Aveiro, Portugal, 3810-193
- School of Health Sciences
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-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- naïve to nervous system mobilization;
Exclusion Criteria:
- Any surgery or trauma in the previous 6 months; neurological, cardiorespiratory or rheumatic pathology; cancer.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Outro
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Solteiro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
---|---|
Experimental: Neural mobilization - tension
It is anticipated that 30 participants will be in this group.
They will receive tension type neural mobilization of the peroneal nerve in the dominant limb.
This will consist of positioning the lower limb with inversion and plantar flexion of the ankle, extension of the knee and maximum flexion of the hip without pain.
A physiotherapists will move the hip from this maximum position of flexion in direction to extension (for example if the participants reaches 80º of flexion the mobilization will be between 40º and 80º of flexion).
Each participant will receive four series of 10 mobilizations with 1 minute rest between series.
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Neural mobilization in tension consists of using combinations of joint movement known to maximize the tension and lengthening of peripheral nervous structures. The intervention will be delivered in one session only. |
Comparador Ativo: Neural mobilization - sliding
It is anticipated that 30 participants will be in this group.
They will receive sliding neural mobilization of the peroneal nerve in the dominant limb.
Each participant will receive four series of 10 mobilizations with 1 minute rest between series of the following combination of movement: from ankle dorsiflexion, knee extension and hip extension to ankle plantarflexion, knee and hip flexion.
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Gliding neural mobilization consists of using combinations of joint movement known to maximize the movement of the peripheral nerves in relation to adjacent structures. The intervention will be delivered in one session only. |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
---|---|---|
Range of motion of the Straight Leg Raising test
Prazo: Baseline
|
The hip is raised to maximum flexion and the degree of flexion is measured with universal goniometer
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Baseline
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Range of motion of the Straight Leg Raising test
Prazo: Approximately 45 minutes after baseline measurements
|
The hip is raised to maximum flexion and the degree of flexion is measured with universal goniometer
|
Approximately 45 minutes after baseline measurements
|
Range of motion of the Straight Leg Raising test
Prazo: At least 24 hours after baseline measurements
|
The hip is raised to maximum flexion and the degree of flexion is measured with universal goniometer
|
At least 24 hours after baseline measurements
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
---|---|---|
Heat threshold
Prazo: Baseline
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Baseline
|
Heat threshold
Prazo: Approximately 45 minutes after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Approximately 45 minutes after baseline measurements
|
Heat threshold
Prazo: At least 24 hours after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
At least 24 hours after baseline measurements
|
Cold threshold
Prazo: Baseline
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Baseline
|
Cold threshold
Prazo: Approximately 45 minutes after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Approximately 45 minutes after baseline measurements
|
Cold threshold
Prazo: At least 24 hours after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
At least 24 hours after baseline measurements
|
Pressure pain threshold
Prazo: Baseline
|
This is measured using a pressure pain algometer.
Pressure is made with this device against a specific body region (upper and lateral part of the dominant foot) until the participants perceives that the pressure changes to pain.
The amount of pressure that the participants perceives as being painful is the test result.
|
Baseline
|
Pressure pain threshold
Prazo: Approximately 45 minutes after baseline measurements
|
This is measured using a pressure pain algometer.
Pressure is made with this device against a specific body region (upper and lateral part of the dominant foot) until the participants perceives that the pressure changes to pain.
The amount of pressure that the participants perceives as being painful is the test result.
|
Approximately 45 minutes after baseline measurements
|
Pressure pain threshold
Prazo: At least 24 hours after baseline measurements
|
This is measured using a pressure pain algometer.
Pressure is made with this device against a specific body region (upper and lateral part of the dominant foot) until the participants perceives that the pressure changes to pain.
The amount of pressure that the participants perceives as being painful is the test result.
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At least 24 hours after baseline measurements
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Anabela Silva, PhD, University of Aveiro
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Outros números de identificação do estudo
- NSM01
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
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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