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Multimodal Exercise and Education Program in Metastatic Breast CancerMostrar más líneas

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.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07693985
Acronym
MBC_MME
Enrollment
37
Registered
2026-07-09
Start date
2024-01-12
Completion date
2025-12-17
Last updated
2026-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer-Related Fatigue, Metastatic Breast Cancer, Quality of Life

Keywords

Metastatic breast cancer, Quality of life, Supportive care, Physical exercise, Health education

Brief summary

This longitudinal pre-post study evaluates the effects of a 12-week community-based multimodal intervention combining supervised physical exercise and health education in women with metastatic breast cancer receiving active systemic treatment. The intervention includes Nordic walking, Tai Chi, and structured health education workshops. The main outcomes are changes in health-related quality of life and cancer-related fatigue, assessed before and after the intervention using validated EORTC questionnaires.Mostrar más líneas

Detailed description

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.

Interventions

OTHERMultimodal Oncology-Based Intervention for Metastatic Breast Cancer

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.

Sponsors

University of Valencia
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

No masking was applied. Due to the nature of the community-based physical exercise and health education intervention, participants and intervention providers could not be blinded to group assignment. Outcome assessments were performed before and after the intervention.Mostrar más líneas

Intervention model description

Single-group, longitudinal pre-post interventional study. All participants receive the same 12-week community-based multimodal intervention combining supervised physical exercise and health education. Outcomes are assessed before and after completion of the intervention.Mostrar más líneas

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Global Health Status/Quality of LifeMostrar más líneasBaseline and after completion of the 12-week interventionMostrar más líneasChange 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

Secondary

MeasureTime frameDescription
Change in Physical FunctioningMostrar más líneasBaseline and after completion of the 12-week interventionMostrar más líneasChange 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
Change in Role FunctioningMostrar más líneasBaseline and after completion of the 12-week interventionMostrar más líneasChange 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
Change in Emotional FunctioningMostrar más líneasBaseline and after completion of the 12-week interventionMostrar más líneasChange 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.
Change in Cancer-Related FatigueMostrar más líneasBaseline and after completion of the 12-week interventionMostrar más líneasChange 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
Change in Multidimensional FatigueMostrar más líneasBaseline and after completion of the 12-week interventionChange 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
Change in Breast Cancer-Specific Quality of LifeMostrar más líneasBaseline and after completion of the 12-week interventionMostrar más líneasChange 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

Countries

Spain

Contacts

PRINCIPAL_INVESTIGATORSergio Pascual-Solaz

a. Departament of Medical Oncology, Consorcio Hospital Provincial, Castellón 12005 Valencia, Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 10, 2026