Semi-supervised Exercise Program Before Bariatric Surgery
Effects of Exercise on Body Composition, Cardiovascular Risk Factors and Surgery Complications in Bariatric Patients
Background: Patients awaiting bariatric surgery, apart from suffering higher BMI, show a large number of comorbidities and a low physical fitness. These factors are associated with a longer surgery time, a longer hospital stay and a greater number of operative complications. To reduce these disadvantages, a nutritional intervention is performed to reduce total weight and the comorbidities associated with obesity prior to surgery. However, the prescription of an exercise program, which can be an effective tool to improve these factors, is not usually part of the usual care of these patients.
Objective: To know the effects of a semi-supervised exercise program on body composition, cardiovascular risk factors and operative complications in bariatric patients.
Methods: Approximately 3 months before surgery, 60 patients awaiting bariatric surgery will be recruited. Patients will be randomized into two groups: a) an experimental group (n = 30); b) a control group (n = 30). The experimental group will perform a semi-supervised exercise program, while the control group will only perform the corresponding evaluations. Both groups will be assessed for body composition, cardiovascular risk factors, physical condition, quality of life and physical activity levels at the beginning and at the end of the intervention. In addition, surgery time, hospital length of stay and operative complications will be evaluated in both groups.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Antecipado)
Estágio
- Não aplicável
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Age between 20-55 years.
- All patients awaiting bariatric surgery.
Exclusion Criteria:
- Patients with chronic respiratory diseases
- Patients with cardiovascular diseases
- Inability to perform exercise
Plano de estudo
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 |
|---|---|
|
Experimental: Exercise group
Three months of semi-supervised exercise program in patients awaiting bariatric surgery.
Body composition, cardiovascular risk factors, physical fitness, physical activity levels and quality of life will be assessed before and at the end of the study.
In addition, surgery time, hospital length of stay and operative complications also will be evaluated.
|
Twelve-week of semi-supervised exercise program.
The exercise program will combine resistance and endurance training.
Both the volume and intensity of training will start at moderate intensity, and progressively be increased at higher volumes and intensities.
Outros nomes:
|
|
Sem intervenção: Control group
The control group only will perform the evaluations of the study.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change in body composition - Body mass index
Prazo: Baseline and 3 months, between 8:00 AM and 9:00 AM.
|
Bioimpedance analysis will be used for establishing body weight and body composition.
This variables will be evaluated between 8:00 and 9:00 A.M., after at least 8 hours of fasting, with an empty bladder.
Body mass index will be calculated dividing weight in kilograms by squared height in meters.
Therefore, body mass index will be expressed as kg·m-2.
|
Baseline and 3 months, between 8:00 AM and 9:00 AM.
|
|
Change in glucose and HbA1c levels.
Prazo: Baseline and 3 months, between 8:00 AM and 10:00 AM.
|
Blood samples will be taken after a 12 h of overnight fast.
Exercise will be forbidden 48 h before the test.
|
Baseline and 3 months, between 8:00 AM and 10:00 AM.
|
|
Change in total cholesterol, HDL cholesterol and LDL cholesterol levels.
Prazo: Baseline and 3 months, between 8:00 AM and 10:00 AM.
|
Blood samples will be taken after a 12 h of overnight fast.
Exercise will be forbidden 48 h before the test.
|
Baseline and 3 months, between 8:00 AM and 10:00 AM.
|
|
Change in systolic and diastolic blood pressure.
Prazo: Baseline and 3 months, between 8:00 AM and 9:00 AM.
|
Systolic and Diastolic Blood pressure will be measured according to established recommendations.
|
Baseline and 3 months, between 8:00 AM and 9:00 AM.
|
|
Complications rates
Prazo: Day 30 after surgery.
|
All the complications suffered by patients will be recorded.
|
Day 30 after surgery.
|
|
Length of stay.
Prazo: Day 15 after surgery.
|
The number of days at hospital after bariatric surgery will be recorded.
|
Day 15 after surgery.
|
|
Change in handgrip strength
Prazo: Baseline and 3 months, between 5:00 PM and 8:00 PM.
|
Strength levels will be assessed using a hand dynamometer.
|
Baseline and 3 months, between 5:00 PM and 8:00 PM.
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change in physical activity levels.
Prazo: Baseline and 3 months, seven days.
|
Levels of physical activity will be measured recording the physical activity performed for 7 days using an accelerometer.
|
Baseline and 3 months, seven days.
|
|
Change in health-related quality of life: sf-36 questionnaire.
Prazo: Baseline and 3 months.
|
The Spanish version of Short Form Health Survey 36 (SF-36) will be used for knowing changes in quality of life.
This questionnaire uses 8 scales to evaluate physical health (4 scales: Physical Function, Role Physical, Bodily Pain, General Health) and mental health (4 scales: Vitality, Social functioning, Role Emotional, and Mental Health).
The scores of these scales are transformed into values between 0-100 points, where highest scores are related to better function.
These 8 scales are grouped into two summary components (physical summary component; mental summary component) which will be calculated according to the reference values of the Spanish population, with a mean of 50 and standard deviation of 10.population.
|
Baseline and 3 months.
|
|
Change in waist and hip circumference.
Prazo: Baseline and 3 months, between 8:00 AM and 9:00 AM.
|
Waist and hip circumference will be measured in centimeters, using established recommendations.
|
Baseline and 3 months, between 8:00 AM and 9:00 AM.
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Antecipado)
Conclusão Primária (Antecipado)
Conclusão do estudo (Antecipado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
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
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- HRJC-19_Ex.Bar
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
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 .