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- Ensaio Clínico NCT02358915
A Two-step Training Paradigm for Voluntary Control of the Peri-auricular Muscles
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
Survivors of spinal cord injury (SCI) usually have severe mobility limitation due to their paralysis.In order to improve the independence of living for those patients, scientists and engineers invented many different types of assistive devices, such as breath controlled "sip and puff" devices, speech controlled devices, eye movement controlled devices, and head movement controlled devices. However, one limitation of the previous designs is that they all require usurping the intact function of a functional organ like mouth or eyes. A recent design by Reach Bionic's company takes advantage of a set of ear muscles-the peri-auricular muscles-that are present in more than 95% of the population, but do not serve any physiologic function in humans. These muscles are innervated by branches of cranial nerves that are controlled through the brain stem, above the spinal cord. Therefore, it is unlikely they will be affected even by a very high SCI. The design intention is to translate the ear contraction signal from the muscles into the meaningful control signal to direct a wheelchair or operate a computer cursor in a fashion to a joystick or mouse. However, since most people do not have the ability to voluntarily contract their ear muscles, the question remains how to best learn to contract our ear muscles and design an effective training paradigm.
Since norm volunteers will have the same voluntary control of their peri-auricular muscles as the patients suffering from spinal cord injury, thus, the investigators are going to test the effectiveness of our two-step training paradigm among the healthy participants at this explorative stage.
In specific, at the first step of training, participants will be asked to voluntarily contract their ear muscles with the facilitation of electrical stimulation. At the second step of training, they will take part in a computer game and will be asked to move a cursor to a specific target that will randomly appear on the computer screen. The cursor will be controlled by the electrical activities produced by the ear muscles contractions that will be captured by surface electromyography (EMG) signals.
The computer game performance of each participant before and after the second step of training with surface EMG signals feedback and the mean surface EMG signal amplitude of the auricular muscles at the maximum voluntary contraction at baseline, after the first step of training, and after the second step of training will be compared.
Tipo de estudo
Inscrição (Antecipado)
Estágio
- Fase inicial 1
Contactos e Locais
Locais de estudo
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California
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Los Angeles, California, Estados Unidos, 90089
- University of Southern California-Health Sciences Campus
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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:
- healthy participants
- can't control their peri-auricular muscles at the beginning of the study (no visible movement of the ears on command).
Exclusion Criteria:
- Suffering any comorbid neuromuscular disease.
- Having a history of severe traumatic brain injury.
- Demonstrating cognitive impairment that would prevent them from providing inform consent or following the directions of the study protocol.
- Having a history of migraine headaches that could be exacerbated with the use of the electrical stimulation or the prolonged training sessions.
- Temporomandibular Joint (TMJ) dysfunction that could lead to unusual discomfort following training session.
- Having a history of prior seizure.
- Being implanted with pacemaker or defibrillators.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Outro
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
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Experimental: Peri-auricular muscles voluntary contraction training paradigm
The whole training paradigm consists of two steps.
At the first step of training, the electrical stimulation (FastStart neuromuscular electrical stimulator) will be applied to facilitate the voluntary contractions of the ear muscles, and the motion of the outer ear in two directions (up/down, forward/backward) will be videotaped and played back to the participants so that they can get real-time visual feedback about their ear movement.
At the second step of training, surface EMG electrodes will be placed on the skin around participants' ears.
During the training, they are required to move a cursor to a specific target that will randomly appear on the computer screen.
The cursor will be controlled by the electrical signal from the contraction of their bilateral peri-auricular muscles.
In the computer game, contraction of the left ear muscles will move the cursor to the left side and contraction of your right ear muscles will move the cursor to the right side.
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Outros nomes:
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
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The surface EMG signal amplitude of the auricular muscles at the maximum voluntary contraction
Prazo: Up to 5 weeks
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Up to 5 weeks
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Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
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The computer game performance score
Prazo: Up to 2 weeks
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Up to 2 weeks
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Carolee J. Winstein, Ph.D, University of Southern California
- Investigador principal: Baker Lucinda, Ph.D, University of Southern California
Publicações e links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
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
- HS-14-00672
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 .