Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:56 PM
Ignite Modification Date:
2025-12-24 @ 1:56 PM
NCT ID:
NCT05690295
Eligibility Criteria:
Inclusion Criteria:
* Healthy postmenopausal women and postmenopausal women survivors of breast cancer with and without Hormonal Therapy (Aromatase Inhibitors and Tamoxifen) between 45 to 59 years.
* Women survivors of breast cancer with active Hormone Therapy in the last 12 months.
* Women breast cancer survivors with luminal molecular profile and positive estrogen receptors.
* Body mass index 18.5 \< BMI \< 30 kg/m2.
* Volunteers without cognitive impairment (abbreviated Minimental \>13 points).
Exclusion Criteria:
* Active antineoplastic treatment in the last 12 months.
* \>200 mL of volume difference between upper limbs and/or stage IV breast cancer.
* Performing regular resistance training (2 or more times per week, carrying out progressive training) in the previous 6 months.
* Cardiovascular diseases that are contradictory for physical activity (not included controlled Hypertension).
* All co-morbidities interacting with mobility and muscle metabolism of the body and that do not allow to (safely) perform the resistance-type exercise training (e.g. debilitating arthritis, spasticity/rigidity, all neurological disorders and paralysis).
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
45 Years
Maximum Age:
59 Years
Study:
NCT05690295
Study Brief:
Protocol Section:
NCT05690295