Study on the Level of Physical Activity in Patients Diagnosed With Breast Cancer in Spain (GYMNOS Project)

March 17, 2026 updated by: Spanish Breast Cancer Research Group

There is strong evidence demonstrating the benefits that physical activity (PA) provides for patients with breast cancer (BC), both in prevention and throughout various treatments and in survivorship. However, there is still very limited information available regarding the level or amount of PA undertaken by BC patients or survivors. On the other hand, although there are general recommendations for physical exercise- 150-300 minutes per week of moderate activity or 75-150 minutes per week of vigorous activity-the type of physical exercise that is best at each stage of the disease, as well as adherence and preferences for different exercise programs, has not been thoroughly studied.

Physical exercise is a healthy, easily implemented and low-cost intervention that ought to be much more widely adopted among the BC population.

Understanding all these factors will help us better assess the degree of implementation and compliance with exercise programs in our population of BC patients. This diagnosis will be the first step towards establishing new strategies to improve patients' PA levels and their adherence to exercise programs, ultimately ensuring that these changes become consolidated as new lifestyle habits that provide our patients with a preventive factor against relapses, as well as a better quality of life.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

According to data from the latest 2026 annual report by the Spanish Society of Medical Oncology (SEOM), breast cancer is the second leading cause of cancer worldwide (12.3% of cancer cases diagnosed in both sexes). The estimated number of new cases in Spain for 2021 is 38,318. In addition, men account for approximately 1% of all new diagnoses of this disease.

There is strong evidence of the benefits that physical activity (PA) brings to patients with breast cancer, both in prevention and throughout various treatments and survivorship. The latest review by the Physical Activity Guidelines Advisory Committee (PAGAC) in 2018 determined that there is currently robust evidence confirming that PA reduces the risk of developing seven types of cancer, including breast cancer, by between 10% and 24%.

Likewise, the American College of Sports Medicine (ACSM) in March 2018 concluded that there is strong evidence supporting an association between PA and the risk of developing several types of cancer, including breast cancer, as well as survival after the disease.

Evidence from several systematic reviews and meta-analyses shows a consistent inverse relationship between levels of PA after diagnosis and cancer-specific mortality (a 38% reduction) as well as all-cause mortality (a 48% reduction) among breast cancer survivors.

According to current PA guidelines, a minimum of 150-300 minutes per week of moderate activity or 75-150 minutes per week of vigorous activity is recommended. According to various studies, these recommendations are known by only a small percentage of breast cancer patients and survivors.

JUSTIFICATION Breast cancer patients who undergo chemotherapy and/or radiotherapy reduce their PA levels more than patients without adjuvant therapy or with hormonal treatment. There is still very little information providing data on the level or amount of PA undertaken by breast cancer patients or survivors. One of the first studies to objectively evaluate PA and sedentary levels using accelerometry in breast cancer survivors was conducted by Boyle et al. in 2015. Another study, carried out in Ohio with 227 participants, reported a recovery in activity levels from shortly after surgery up to one year later, followed by a reduction in PA five years after surgery. Regarding recreational activity levels, Mason et al. reported a low and relatively constant maintenance of these levels during five years of follow-up.

At the European level, a prospective cohort study in the Netherlands compared PA levels of women with breast cancer during and up to three years after treatment, with those of healthy women of similar age. The results showed that PA levels in women with breast cancer were lower, especially in women undergoing systemic treatment and in older women. From one to three years after diagnosis, women with breast cancer continued to have lower PA levels. In Belgium, a study with 267 breast cancer survivors demonstrated that PA levels decreased in the first year after surgery and remained below preoperative levels two years after the operation.

In Spain, a study involving 386 women evaluated PA levels in breast cancer survivors. The results indicated that most patients do not meet the recommended PA levels.

Regarding preferences on PA, a study conducted in Chile in 2018 with 112 breast cancer patients observed that, in general, patients preferred to exercise with other patients (76%), at moderate intensity (67%), performing different activities (94%), supervised (94%), with a fixed schedule (69%), and to do group activities (90%). Only 13% of patients met the exercise guidelines, and these were the youngest patients and those with a recent diagnosis. In Nova Scotia (Canada), Forbes et al. conducted a study in which it was found that 60% of breast cancer survivors preferred supervised or instructed activities and 53% preferred group sessions.

For all these reasons and given the lack of specific data on this population, it is considered essential to carry out the first study that provides information on the PA levels of breast cancer patients, as well as to determine socio-demographic differences and to identify preferences regarding exercise programs in this group of patients. In this way, it will be obtained a current diagnosis of these variables, serving as a starting point for designing new strategies to adapt current resources and improve adherence to PA.

Study Type

Observational

Enrollment (Actual)

507

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Madrid
      • San Sebastián de los Reyes, Madrid, Spain, 28700
        • Spanish Breast Cancer Research Group (GEICAM)

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients with breast cancer at various stages of the disease. Patients access the questionnaire via a link that redirects them to the GEICAM intranet platform, where the questionnaire is hosted. The dissemination of the link is carried out through GEICAM's channels on social media, its website, and las newsletters de nuestros Asociados y a asociaciones de pacientes.

The dissemination of the link is conducted via GEICAM's channels on social media, GEICAM website, and newsletters for GEICAM members and patient associations.

The involvement of various national patient associations, with whom GEICAM has collaboration agreements, is expected to encourage the participation of as many patients as possible.

Description

Inclusion Criteria:

  • Women and men.
  • Individuals aged 18 years and over.
  • Diagnosis of localized or advanced breast cancer, either undergoing treatment or in follow-up.
  • Patients who are able and willing to complete the questionnaires provided for the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Experimental group
Self-administered questionnaire only once

Patients access the questionnaire via a link that redirects them to the GEICAM intranet platform, where the questionnaire is hosted. The dissemination of the link is carried out through GEICAM's channels on social media, its website, and the newsletters to our members and patient associations.

The dissemination of the link is conducted via GEICAM's channels on social media, GEICAM website, and newsletters for GEICAM members and patient associations.

Additionally, information may be provided in paper format with the participation of our associates. The involvement of various national patient associations, with whom GEICAM has collaboration agreements, is expected to encourage the participation of as many patients as possible.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To analyze the level of physical activity (PA) of Spanish patients diagnosed with breast cancer (BC) through self-administered questionnaires
Time Frame: Day 1
The primary objective is assessed using the International Physical Activity Questionnaire (IPAQ). This questionnaire is a standardized instrument for measuring physical activity levels over the previous seven days. The long form comprises 27 to 31 detailed items covering work, transportation, household tasks, gardening, and leisure activities, with results classified in metabolic equivalents (METs) to categorize activity as low, moderate, or high. The questions are based on the number of days per week participants engage in specific physical activities and the duration of each activity.
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ascertain the preferences of Spanish patients diagnosed with breast cancer regarding physical exercise programs
Time Frame: Day 1
To determine patients' preferences regarding exercise programs, data from the section of the questionnaire entitled "Preference Questionnaire for an Exercise Program" will be analyzed. These questions have been adapted from previous studies, corresponding to questions 2 to 12 (From whom do you prefer to receive exercise advice? How would you prefer to receive this advice? When would you like to start the exercise program? With whom would you prefer to exercise? Where do you prefer to exercise? What intensity do you prefer? Do you prefer the type of exercise in each session to be the same or different? Do you prefer supervision from a professional? Do you prefer a fixed or flexible schedule? At what time of day would you prefer to exercise? Do you prefer the activity to be performed individually or group-based?
Day 1
Assess sociodemographic differences in physical activity levels and references concerning physical exercise programs
Time Frame: Day 1
To evaluate sociodemographic differences in relation to physical activity levels and preferences regarding physical exercise programs, sociodemographic data have been collected to be correlated with the responses obtained through the questions in the IPAQ-Long Form (LF) questionnaire.
Day 1
Evaluate differences in physical activity levels in relation to breast cancer treatment
Time Frame: Day 1
To assess differences in physical activity levels in relation to breast cancer treatment, clinical data were collected from patients to be correlated with the responses obtained through the questions in the IPAQ-LF questionnaire.
Day 1
Assess the influence of breast cancer diagnosis on physical activity levels and other lifestyle habits.
Time Frame: Day 1
To assess the influence of a breast cancer diagnosis on physical activity levels and other lifestyle habits, specific questions were asked regarding tobacco use, alcohol consumption, diet, and physical activity. The questionnaire includes a specific question: "Has the diagnosis of breast cancer affected your habits?" For each item (tobacco use, alcohol consumption, diet, sleep quality, social activity and physical activity), the response options are: better than before, worse than before, the same as before, do not know/do not answer.
Day 1
Determine the degree of knowledge among patients diagnosed with breast cancer regarding the minimum recommended level of physical activity according to international guidelines.
Time Frame: Day 1
To determine the level of knowledge among patients diagnosed with breast cancer regarding the minimum physical activity recommended by international guidelines, a specific question was included asking whether they were aware of the minimum recommendations and what those recommendations were. The question is as follows: Are you aware of the minimum recommended amount of physical activity (minutes per week) according to the World Health Organization? The possible responses are: yes (please indicate the number of minutes of moderate and vigorous physical activity) or no.
Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Study Director Study Director, Complejo Hospitalario Universitario A Coruña (CHUAC)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 8, 2025

Primary Completion (Actual)

May 31, 2025

Study Completion (Actual)

May 31, 2025

Study Registration Dates

First Submitted

March 12, 2026

First Submitted That Met QC Criteria

March 12, 2026

First Posted (Actual)

March 18, 2026

Study Record Updates

Last Update Posted (Actual)

March 20, 2026

Last Update Submitted That Met QC Criteria

March 17, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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