Physical Activity and Cardiovascular Risk in Breast Cancer Survivors
Data Collection
Collected from today forward - ProspectiveBehavior+6
+ Breast Diseases
+ Breast Neoplasms
Other
Utilizing specific methods not covered by standard models in order to address unique research questions.Summary
Study start date: July 30, 2024
Actual date on which the first participant was enrolled.This study explores the connection between physical activity levels and cardiovascular health in breast cancer survivors. Cardiovascular disease (CVD) is a major cause of illness and death globally, and it increasingly affects individuals after surviving breast cancer, especially as they age. Regular physical activity is known to lower many risk factors for CVD, such as high blood pressure and stress, and improve overall health. For breast cancer survivors, engaging in physical activity during and after treatment can enhance survival rates and quality of life. However, there is limited evidence on how physical activity impacts long-term cardiovascular outcomes in these individuals. This study aims to find the best types of physical activities and assess how different activity levels affect cardiovascular risks in various age groups of breast cancer survivors. Participants in this study will have their physical activity levels measured using the SenseWear Armband, a device worn for at least seven days to track movement and energy expenditure. The study will gather detailed demographic information such as age, medical history, and lifestyle habits, and assess participants' cardiovascular risk using the SCORE2 system. This system evaluates risk based on factors like cholesterol levels and blood pressure. Additionally, the study will measure participants' exercise capacity through a six-minute walking test and evaluate their quality of life and anxiety levels using standardized questionnaires. By analyzing these factors, the study aims to better understand the role of physical activity in managing cardiovascular health in breast cancer survivors, potentially leading to improved health outcomes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.70 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 40 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: 1. To be between the ages of 40-80 years, 2. Volunteering to participate in the research, 3. At least 15 months after breast cancer surgery, 4. 6 months after active breast cancer treatment (ie surgery/chemotherapy) 5. Having no problem in reading and/or understanding the scales and being able to cooperate with the tests. Exclusion Criteria: 1. Presence of active infection, 2. Having a neurological disease or other clinical diagnosis that may affect cognitive status, 3. Having musculoskeletal and neurological disease, symptomatic heart disease, previous lung surgery and malignant disease that may affect exercise performance. 4. Presence of unstable hypertension or diabetes mellitus
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location