Impact of Physical Exercise on Lymphedema Related to Breast Cancer: Assessment Using Thermography

Study Type: Clinical Trial Primary Purpose: To determine whether physical exercise improves or prevents lymphedema in breast cancer patients. Description of the Participant Population/Main Condition: The study is aimed at women who have been diagnosed with breast cancer and have experienced post-treatment lymphedema or are at risk of developing it. The target population includes adults aged 18 to 70 who have been diagnosed with this condition following their breast cancer treatment. Main Research Questions: Does physical exercise improve or prevent lymphedema in women with breast cancer? What are the effects of physical exercise on the reduction of arm volume affected by lymphedema? What are the effects of physical exercise on the reduction of perceived disability in the arm affected by lymphedema? Hypothesis: Physical exercise intervention significantly reduces lymphedema symptoms, such as arm volume. Physical exercise prevents the progression of lymphedema in women with breast cancer. Comparison Group: Researchers will compare results between the experimental group (which will undergo physical exercise) and the control group (which will receive no intervention) to determine if physical exercise has a significant impact on the improvement or prevention of lymphedema. Participant Tasks: The experimental group will follow a supervised physical exercise program for a specific period. The control group will receive no intervention and will be monitored with standard follow-up care without exercise. Participants will be evaluated before and after the study period to measure the progression of lymphedema, including arm volume measurement and surface skin temperature using thermography.

Sex

All

Minimum age

18 Years

Inclusion Criteria:

* Women over 18 years old diagnosed with breast cancer.
* Residing in the province of León.
* Not currently undergoing any physical exercise intervention at the time of the study.
* Not participating in lifestyle modification programs at the time of the study.
* Not presenting any relative or absolute sequelae from chemotherapy treatment that would pose a relative or absolute contraindication to their participation in this intervention (e.g., cardiological sequelae).
* Having signed the informed consent to participate in the study.

Exclusion Criteria:

* Presenting physical and/or psychological limitations that would hinder understanding or the ability to carry out the established intervention program.
* Presenting an infection in the upper limbs or lymphangitis.
* Fluid accumulation in the breast area requiring drainage at the time of the intervention.
* Not having signed the informed consent to participate in the study