Cycle Ergometer Exercise in Phase I of Cardiac Rehabilitation After Cardiac Surgery
28 de janeiro de 2021 atualizado por: Ada Clarice Gastaldi, University of Sao Paulo
The prevalence of heart diseases has increased significantly in recent years and it is a health public problem due to an increased risk of death by several reasons.
A cardiac surgery is an alternative of treatment for critical injuries heart valves and coronaries arteries.
Changes in respiratory system resulting from cardiac surgery are well established and include a reduced functional capacity due post-surgical pain, causing increased respiratory function and increased oxygen consumption .
The exercises with the cycle ergometer in phase I of cardiac rehabilitation can improve peripheral muscle strength, functional capacity and perception of dyspnea when used postoperatively and there are speculations if an earlier carried out can contribute to a better postoperative evolution of patients, but these benefits in phase I of the Rehabilitation Cardiac are not well defined in the literature.
Objective: To evaluate the exercises effects with ergometer cycle in the postoperative course of patients undergoing cardiac surgery.
Method: Patients will be recruited the cardiac surgery service of Polyclinic Pato Branco in the city of Pato Branco in state of Paraná, of both sexes, appropriate for the inclusion criteria, which will be evaluated by pulmonary function tests (strength of respiratory muscles, submaximal exercise test, dyspnea scales, laboratories tests and radiological exam).
All patients will be randomly assigned for one of two groups: the control group (Conventional treatment) and rehabilitation group (conventional treatment +cycle ergometer), for about 7 days at postoperative period.
Patients will be reevaluated on the third postoperative day and at discharge.
Clinical evolution data will be collected from the records and notes of the medical staff and monitoring physiotherapist.
Visão geral do estudo
Status
Retirado
Intervenção / Tratamento
Descrição detalhada
The research will be a randomized controlled clinical trial.
The study will be conducted at the Polyclinic Pato Branco, in the city of Pato Branco Parana - Brazil and this study already approved by the Ethics Committee Clinical Hospital and Faculty of Medicine, University of São Paulo and all participants sign the consent form informed.
For the implementation of research wil be recruited patients heart surgery who fit the inclusion criteria and do not show any characteristics of the exclusion criteria, which agree to participate and sign the consent form free and informed.
The equipment and tests are already included in routine admissions of patients, approved by the hospital and the Brazilian Public Health System (SUS).
Tipo de estudo
Intervencional
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
-
-
Paraná
-
Pato Branco, Paraná, Brasil, 85501250
- Policlínica Pato Branco
-
-
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
30 anos a 70 anos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Não
Gêneros Elegíveis para o Estudo
Tudo
Descrição
Inclusion Criteria:
- Patients undergoing cardiac surgery type Myocardial Revascularization and Exchange Mitral Valve Aortic, both sexes and aged between 30-75 years.
Exclusion Criteria:
Patients undergoing surgical correction of heart disease congenital, aortic aneurysm and dissection of aorta;
- Present disabling disease to accomplish what is proposed in study as previous stroke, mental or motor deficit, hearing loss, amputation of the lower limbs (unilateral or bilateral);
- Present psychomotor agitation of immediate postoperative and first postoperative and history weaning failure in the immediate;
- Instability hemodynamics and vasoactive drugs;
- Present what other type of peri and postoperative complications;
- Re-operation within 24 hrs.
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 de Placebo: Control group: routine physiotherapy
Are patients who carry out the routine already established the Unit, consisting of the first post surgery, the patient lying down doing the breathing exercises, active exercises ends and active-assisted upper (UL) and lower limbs (LL),
|
routine physiotherapy
|
|
Comparador Ativo: Intervention group: ergometer cycle exercise
Are the patients who will carry out the exercises routine over the cycle ergometer twice daily from 3 PO for 5 minutes with its progressiveness at discharge for ward for 10 minutes
|
routine physiotherapy
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change of six-minute walk test (6MMWT) distance
Prazo: Before surgery ,third and seventh postoperative day
|
The six-minute walk test will be conducted with monitoring blood pressure, HR, RR and SpO2 in a hall plan, with distances previously marked.
The patient will be accompanied by the researcher and encouraged by constant verbal stimulation, walking as fast as possible, if the patient stop walking the timer will keep triggered.
Will use the oximeter with the sensor on the third finger of the right hand, and a certain reading after the signal stabilization and at the same time we get the heart rate.
Will be used to calculate the expected value, and reference to distance in the 6MWT, the equations proposed by Enright and Sherrill (1998) determining the percentage of predicted for each test performed by patient.
|
Before surgery ,third and seventh postoperative day
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change of spirometric values
Prazo: Before surgery ,third and seventh postoperative day
|
Spirometry will be performed according to criteria of the American Thoracic Society and the Brazilian Consensus Spirometry.
Values will be observed from CVF, VEF1 e PEF.
|
Before surgery ,third and seventh postoperative day
|
Outras medidas de resultado
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change of respiratory muscle strength - Mouth pressure measurements
Prazo: Before surgery ,third and seventh postoperative day
|
Manovacuometry will be performed with the patient seated with nasal clip, the display scale with intervals of 4 cmH2O and variation +/- 120 cmH2O.
The highest value obtained during the two maneuvers will be compared to the table described by Neder et al (1999), which predicts expected values for the Brazilian population according to gender and age.
|
Before surgery ,third and seventh postoperative day
|
|
Change of perceived dyspnea
Prazo: Before surgery ,third and seventh postoperative day
|
The perceived effort is used the Borg Scale modified scored from 0 to 10.
And dyspnea scale will be scored from 0 to 4 according to the intensity of dyspnea and is based on used the scale of the Medical Research Council (MRC).
|
Before surgery ,third and seventh postoperative day
|
|
Change of body mass index
Prazo: Before surgery and postoperative seventh day
|
The BMI will be calculated using the classical formula: BMI = current weight (kg) / A2 (m).
The following lower limits of normal were considered: BMI <21 for age group 35-44 years; <22 for 45-54 years; <23 for 55 -64 years and <24 to 65 above years.
|
Before surgery and postoperative seventh day
|
|
Change of cirtometry
Prazo: Before surgery ,third and seventh posoperative day
|
Cirtometry will be held in myocardial revascularization of patients who use the saphenous and waist hip will be performed in all patients.
Will be used a tape measure.
|
Before surgery ,third and seventh posoperative day
|
|
Change of peripheral muscle strength
Prazo: Before surgery ,third and seventh postoperative day
|
The peripheral muscle strength assessment test will be the end of the test the foot, the patient will be instructed to stay barefoot with his right hand resting on the front wall and with a semi elbow flexion to aid maintenance balance.
Prior to testing, the participant will be oriented make a plantar flexion to the point of support of the joints metatarsophalangeal and this time will be marked by the examiner through a mark on the wall and the patient will be informed that should reach the one marked point.
The test itself consisted of time, in seconds, the time it takes to perform five push-ups as plantar soon as possible.
|
Before surgery ,third and seventh postoperative day
|
|
Change in cortisol levels
Prazo: Before surgery ,third and seventh postoperative day
|
Laboratory evaluation will be performed by laboratory staff of hospital with a blood sample from the patient, which will be assessed the cortisol levels .
|
Before surgery ,third and seventh postoperative day
|
|
change of radiological assessment
Prazo: Before surgery ,third and seventh postoperative day
|
Radiological assessment will be held the day before the surgery, the third post-operative and post-operative seventh, the clinic Radiology Southwest - Pato Branco - Paraná to assess complications lung from surgery.
|
Before surgery ,third and seventh postoperative day
|
|
Adherence evaluation
Prazo: Third and seventh postoperative day
|
The questionnaire will be administered at the end of the first contact of the patient the exercises with the cycle ergometer to assess adherence running a differential exercise during your surgical recovery.
|
Third and seventh postoperative day
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Publicações e links úteis
A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.
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
Conclusão Primária (Real)
28 de janeiro de 2021
Datas de inscrição no estudo
Enviado pela primeira vez
29 de abril de 2015
Enviado pela primeira vez que atendeu aos critérios de CQ
6 de maio de 2015
Primeira postagem (Estimativa)
7 de maio de 2015
Atualizações de registro de estudo
Última Atualização Postada (Real)
2 de fevereiro de 2021
Última atualização enviada que atendeu aos critérios de controle de qualidade
28 de janeiro de 2021
Última verificação
1 de janeiro de 2021
Mais Informações
Termos relacionados a este estudo
Outros números de identificação do estudo
- USP 2015-1
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 .
Ensaios clínicos em Cirurgia cardíaca
-
Assiut UniversityAinda não está recrutandoCardiac CT TOF