Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Baptist Health South Florida
* Primary endpoint: To examine the effects of a practical lifestyle intervention that can be implemented by overweight or obese women (BMI greater or equal to 25) with early stage breast cancer (I-III) on outcomes such as body weight and change in BMI over the course of the study.
* Secondary endpoint: To assess the impact of such intervention on lipid profiles and hemoglobin A1C. The study group will be compared with a historical control group of patients with early stage breast cancer who are obese or overweight who were not given the intervention
* Secondary endpoint: To examine whether an active intervention program will lead into longstanding lifestyle modification in breast cancer patients with a BMI greater or equal to 25.
Age
18–89
Sex
FEMALE
Healthy volunteers
Accepted
You may be eligible if
DCIS
Women with stage 0 - III breast cancer (histologic type ductal or lobular)
BMI \>=25
Patients must have completed all chemotherapy
Patients may be on hormonal therapy or radiation therapy
Age \>= 18 years old to 89 Years old
Patient must be medically stable and without significant impairments that would preclude following the proposed intervention regimen.
Time of diagnosis: patients enrolled are within 1 month to 18 months post-diagnosis.
You may not be if
Metastatic breast cancer patients and patients with inoperable or active loco-regional disease.
Patients following alternative/complementary diets or taking high dose antioxidant supplements.
Patients with a physical/psychiatric impairment that would seriously impair their physical mobility.
Patients who are currently suffering from severe nausea, anorexia or other diseases affecting health (e.g. arthritis and multiple sclerosis).
Patients younger than 18 and older than 89 years.
Clareo Health | A Study of Lifestyle Intervention in Overweight or Obese Women With Early Stage Breast Cancer
