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Impact of Personalized and Remote Support Centered on Exercise and Physical Activity for Breast Cancer Patients

Breast Cancer Female Clinical Trial

Official title:
Randomized Study Estimating the Impact of a Personalized and Remote Support Centered on Exercise and Physical Activity for Patients After Breast Cancer

Clinical Trial Summary

A study that evaluates the benefits of a personalized remote exercise and physical activity coaching compared with the standard supportive approach in terms of health-related quality of life at 12 months in breast cancer survivors treated in an adjuvant setting.

Clinical Trial Description

A multicentric, phase III, randomized open-labelled study with two parallel groups which evaluates the benefits of a personalized remote exercise and physical activity coaching compared with the standard supportive approach in terms of health-related quality of life at 12 months in breast cancer survivors treated in an adjuvant setting. Other objectives include: - To evaluate the impact of the intervention on each dimension of the SF-36 at 12 months - To evaluate the impact of the program on the health-related quality of life over time - To evaluate the impact of the program on the practice of exercise and physical activity (EPA) at the recommended intensity (30min of moderate EPA, 5 days/week) - To evaluate the impact of the program on: o fatigue, pain, depression, sleep, motivation for the practice, self-respect, biometric measures (including fat mass and lean mass), physical capacities, patient's satisfaction regarding the assigned program, occurrence of Adverse Events (AE) related to the treatment, professional life for patients who worked before the announcement of getting cancer and psychotropic and analgesic drug intake - To evaluate the compliance to the program through the engagement score during the first 4 months (in the experimental group). - To evaluate the impact of the program in terms of disease-free survival Additional objectives on health economics include: - To evaluate the efficiency of the personalized remote exercise and physical activity coaching compared with the standard supportive approach in BC survivors treated in an adjuvant setting. - To characterize the health-state utility of BC survivors over time; assessing the association of change in health-utility with changes in other variables such as exercise and physical activity. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04536584
Study type Interventional
Source Centre Oscar Lambret
Contact
Status Active, not recruiting
Phase N/A
Start date December 18, 2020
Completion date December 2024
View Details
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