Multimodal Exercise and Education Program in Metastatic Breast CancerMostrar más líneas (MBC_MME)
Effects of a Multimodal Community-based Intervention Combining Physical Exercise and Health Education Workshops on Quality of Life in Women With Metastatic Breast Cancer: a Longitudinal Pre-post Study.
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
Women with metastatic breast cancer receiving active systemic treatment frequently experience impaired health-related quality of life, cancer-related fatigue, and limitations in daily functioning. Supportive care strategies that combine physical exercise, education, and symptom self-management may help improve these outcomes, although evidence in women living with metastatic breast cancer remains limited.
This study is a longitudinal pre-post intervention study conducted in women with metastatic breast cancer receiving active systemic treatment. Eligible participants are women with metastatic breast cancer, preserved functional status, and the ability to ambulate independently. Participants are assessed at baseline and after completion of the intervention.
The intervention lasts 12 weeks and consists of a community-based multimodal program combining supervised physical exercise and health education. The exercise component includes two 60-minute supervised sessions per week: one session of Nordic walking and one session of Tai Chi. Nordic walking sessions are supervised by a physiotherapist, and Tai Chi sessions are led by a trained instructor. Exercise sessions are adapted to participants' physical capacity and clinical condition.
In addition to the exercise component, participants attend structured health education workshops throughout the program. These sessions address topics relevant to women with metastatic breast cancer, including general aspects of metastatic breast cancer, systemic treatments and toxicity management, the benefits of physical exercise, nutrition and supplementation, sleep hygiene, emotional regulation, communication with the social environment, and aesthetic care during cancer treatment.
Health-related quality of life is assessed using the EORTC QLQ-C30 and the breast cancer-specific EORTC QLQ-BR45 questionnaires. Cancer-related fatigue is assessed using the EORTC QLQ-FA12 questionnaire. The study evaluates changes in global health status, functional domains, fatigue dimensions, and selected breast cancer-specific symptom and functional domains before and after the intervention.
The aim of the study is to determine whether a supervised, community-based multimodal program combining physical exercise and health education is associated with improvements in quality of life, functioning, and fatigue-related outcomes in women with metastatic breast cancer receiving active systemic treatment.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
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Valencia, Espanha, 46010
- Carmen García Gomariz
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Women diagnosed with metastatic breast cancer.
- Receiving active systemic treatment.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
- Able to ambulate independently.
- Able and willing to participate in the multimodal intervention program.
- Provided written informed consent.
Exclusion Criteria:
- Moderate or severe cognitive impairment.
- Severe psychiatric illness.
- Sensory impairment preventing participation in the intervention or assessments.
- Chronic disabling conditions limiting participation in the planned activities.
- Unstable bone metastases, according to medical judgment, associated with risk of fragility fracture.
- Cardiac or respiratory disease limiting the capacity to perform physical activity.
- Any other medical condition that, in the opinion of the treating oncologist, contraindicated participation in the program.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- 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: Multimodal Exercise and Health Education Program
Participants receive a 12-week community-based multimodal intervention combining supervised physical exercise and health education.
The exercise component includes one weekly Nordic walking session and one weekly Tai Chi session, each lasting 60 minutes.
In addition, participants attend structured health education workshops addressing topics related to metastatic breast cancer, systemic treatment and toxicity management, physical exercise, nutrition, sleep hygiene, emotional regulation, communication, and aesthetic care during cancer treatment.
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Participants receive a 12-week community-based multimodal oncology intervention combining supervised physical exercise and health education.
The exercise component consists of one weekly Nordic walking session and one weekly Tai Chi session, each lasting 60 minutes.
In addition, participants attend structured health education workshops covering metastatic breast cancer, systemic treatment and toxicity management, safe physical exercise, nutrition, sleep hygiene, emotional regulation, communication, and aesthetic care during cancer treatment.
The intervention aims to promote physical and emotional well-being, support self-management, and improve quality of life.
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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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Change in Global Health Status/Quality of LifeMostrar más líneas
Prazo: Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in global health status/quality of life assessed using the EORTC QLQ-C30 global health status scale.
Scores are transformed to a 0-100 scale, with higher scores indicating better global health status and quality of life.Mostrar más líneas
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Baseline and after completion of the 12-week interventionMostrar más líneas
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Change in Physical FunctioningMostrar más líneas
Prazo: Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in physical functioning assessed using the EORTC QLQ-C30 physical functioning scale.
Scores are transformed to a 0-100 scale, with higher scores indicating better physical functioning.Mostrar más líneas
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Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in Role FunctioningMostrar más líneas
Prazo: Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in role functioning assessed using the EORTC QLQ-C30 role functioning scale.
Scores are transformed to a 0-100 scale, with higher scores indicating better role functioning.Mostrar más líneas
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Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in Emotional FunctioningMostrar más líneas
Prazo: Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in emotional functioning assessed using the EORTC QLQ-C30 emotional functioning scale.
Scores are transformed to a 0-100 scale, with higher scores indicating better emotional functioning.
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Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in Cancer-Related FatigueMostrar más líneas
Prazo: Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in fatigue assessed using the fatigue symptom scale of the EORTC QLQ-C30.
Scores are transformed to a 0-100 scale, with higher scores indicating greater fatigue symptom burden.Mostrar más líneas
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Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in Multidimensional FatigueMostrar más líneas
Prazo: Baseline and after completion of the 12-week intervention
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Change in multidimensional cancer-related fatigue assessed using the EORTC QLQ-FA12 questionnaire, including physical fatigue, emotional fatigue, cognitive fatigue, interference with daily life, and social dimension.
Scores are transformed to a 0-100 scale, with higher scores indicating greater fatigue or impairment.Mostrar más líneas
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Baseline and after completion of the 12-week intervention
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Change in Breast Cancer-Specific Quality of LifeMostrar más líneas
Prazo: Baseline and after completion of the 12-week interventionMostrar más líneas
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Change in breast cancer-specific quality of life assessed using selected domains of the EORTC QLQ-BR45 questionnaire, including body image, future perspective, systemic therapy side effects, arm symptoms, breast symptoms, endocrine therapy symptoms, and skin and mucosal symptoms.
Scores are transformed to a 0-100 scale.
Higher scores indicate better functioning in functional scales and greater symptom burden in symptom scales.Mostrar más líneas
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Baseline and after completion of the 12-week interventionMostrar más líneas
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Sergio Pascual-Solaz, a. Departament of Medical Oncology, Consorcio Hospital Provincial, Castellón 12005 Valencia, Spain
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 (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
Palavras-chave
Termos MeSH relevantes adicionais
- Neoplasias por local
- Neoplasias
- Doenças de pele
- Doenças da mama
- Comportamento
- Doenças da Pele e do Tecido Conjuntivo
- Adesão e Cumprimento do Tratamento
- Comportamento de saúde
- Conformidade do paciente
- Aceitação dos Cuidados de Saúde pelo Paciente
- Intervenções de adesão
- Adesão à Medicação
- Neoplasias da Mama
- Atividade motora
- Educação saudável
Outros números de identificação do estudo
- MBC_MME01
Plano para dados de participantes individuais (IPD)
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Descrição do plano IPD
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