Effects of Combined Cycle Training and Inspiratory Muscle Training in Patients With COPD
16 de maio de 2017 atualizado por: Zhujiang Hospital
Effects of Combined Cycle Training and Inspiratory Muscle Training on Exercise Performance ,Health-related Quality,Dyspnoea ,Body Composition,Depressive Symptomatology in Patients With Chronic Obstructive Pulmonary Disease(COPD)
Chronic Obstructive Pulmonary Disease (COPD) ，the fourth leading cause of death in the world, represents an important public health challenge. It is also a major cause of chronic morbidity, mortality and disability throughout the world, leading to a heavy social and economic burden. For a long time, treatment of COPD mainly focus on drug therapy. Recently, pulmonary rehabilitation is recognized as a core component of the management of individuals with chronic respiratory disease, which has been clearly demonstrated to reduce dyspnea, increase exercise capacity, and improve quality of life.
Exercise training, widely regarded as the cornerstone of pulmonary rehabilitation , is one of the best available means of improving muscle function in COPD.The most commonly form is cycle training. Inspiratory Muscle Training (IMT) as an adjunct to exercise training has an additional benefit on inspiratory muscle strength, endurance and exercise capacity in patient with COPD.
There is insufficient evidence demonstrate greater benefits from combined inspiratory muscle training and cycle training. This study will evaluate the effects of combined inspiratory muscle training and cycle training in patients with COPD.
Visão geral do estudo
Status
Concluído
Descrição detalhada
The patients with COPD will participate in a rehabilitation program for 8 weeks. Participants in the proposed study will be randomly programmed into one of three intervention groups:
- Cycle training program alone (performing on calibrated stationary cycle ergometer).
- Combined cycle training and inspiratory muscle training(performing on calibrated stationary cycle ergometer and threshold loading device).
- Neither cycle training nor inspiratory muscle training.
Tipo de estudo
Intervencional
Inscrição (Real)
90
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.
Locais de estudo
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Guangdong
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Guangzhou, Guangdong, China, 510282
- Zhujiang Hospital,Southern Medical Universtiy
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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
40 anos a 75 anos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Inclusion Criteria:
Patients between 40 and 75 years of age were eligible if they met the following criteria:
- moderate to severe airflow obstruction (30≤ Forced Expiratory Volume At One Second(FEV1) <80% predicted and Forced Expiratory Volume At One Second/Forced Vital Capacity(FEV1/FVC)<70%)
- Complaints of dyspnea on exertion
- Clinically stable condition
- No participation in a pulmonary rehabilitation program in the last year.
Exclusion Criteria:
- Patients were excluded if they had evidence of asthma and/or had experienced a major exacerbation in the 2 months before enrollment
- Required home oxygen therapy or experienced oxyhemoglobin desaturation below 85% with exercise
- And/or had other health problems that would interfere with exercise.
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: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Grupo de controle
Nem treino de ciclismo nem treino de músculos inspiratórios.
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Nem treino de ciclismo nem treino de músculos inspiratórios.
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Experimental: Cycle training group
A 30-minute cycling training session is performed 3 days a week using calibrated cycle ergometer.
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The most common device to proform cycle training is calibrated cycle ergometer.
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Experimental: Combined group
A 30-minute Combined training session is performed 3 days a week using calibrated cycle ergometer and threshold loading device.
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Combined cycle training and inspiratory muscle training.The threshold loading device is composed of a mouth -piece attached to a small plastic cylinder that contains a spring-loaded poppet value.
The valve opens to permit inspiratory flow only once the person has generated adequate negative intrathoracic pressure to condense the spring.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Exercise Performance (composite outcome measure)
Prazo: The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Exercise performance tests include field walking tests and cycle ergometer tests.
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The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Health-related quality (composite outcome measure)
Prazo: The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Health-related quality is a component of the broader concept of quality of life and is defined as satisfaction with health.The St. George's Respiratory Questionnaire (SGRQ) and Chronic Respiratory Disease Questionnaire (CRQ）; and its self-reported version are the most widely used disease-specific questionnaires.
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The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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inspiratory muscle function (composite outcome measure)
Prazo: The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Currently, a variety of methods can be used to evaluate respiratory muscle function, including maximal inspiratory (PImax)，expiratory pressures(PEmax) and inspiratory muscle endurance.
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The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Symptom Evaluation (composite outcome measure)
Prazo: The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Individuals with chronic respiratory disease often have symptoms such as dyspnea, fatigue, cough, weakness, sleeplessness,and psychological distress.Instruments for assessment of multiple symptoms include COPD Assessment Test (CAT) and Modified Medical British Research Council Scale(mMRC).
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The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Depression and anxiety evaluation
Prazo: The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Hospital Anxiety and Depression Scale (HADS) was found to perform well in assessing the symptom severity and caseness of anxiety disorders and depression in both somatic, psychiatric and primary care patients and in the general population.
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The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Composite outcomes
Prazo: The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Among patients with COPD there is increasing interest in the use of multidimensional indices to characterize the severity of the disease and better predict outcomes.Arguably the most well-known of these indices is the BODE Index.
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The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Body Composition Monitor
Prazo: The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Body composition abnormalities are prevalent in COPD.Human body composition analyzer can detect various elements of human body and analyze human health status.
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The groups will be assessed at baseline (time zero) and at the end of the training protocol (week 8)
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Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
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
1 de dezembro de 2014
Conclusão Primária (Real)
1 de janeiro de 2017
Conclusão do estudo (Real)
1 de janeiro de 2017
Datas de inscrição no estudo
Enviado pela primeira vez
20 de julho de 2014
Enviado pela primeira vez que atendeu aos critérios de CQ
24 de julho de 2014
Primeira postagem (Estimativa)
25 de julho de 2014
Atualizações de registro de estudo
Última Atualização Postada (Real)
18 de maio de 2017
Última atualização enviada que atendeu aos critérios de controle de qualidade
16 de maio de 2017
Última verificação
1 de março de 2016
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- CX13902205193
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
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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