Exercise as a Preventive Agent to Combat Immobility in Patients with Ovarian or Endometrial Cancers Receiving Chemotherapy
Trial Description
The purpose of this research is to determine whether a 16-week virtually supervised aerobic
and resistance exercise program is feasible in patients receiving first-line chemotherapy
after surgery for ovarian or endometrial cancer and if it will improve lower extremity
function (function of the legs), lessen chemotherapy-induced peripheral neuropathy (CIPN;
numbness or tingling in the hands or feet), and if there is any effect on inflammatory blood
markers (the level of a certain marker in the blood that is associated with inflammation;
redness and swelling).
Eligibility Requirements
Inclusion Criteria:
- Newly diagnosed patients with stages III-IV ovarian or endometrial cancer
- Receiving first-line carboplatin and paclitaxel chemotherapy after surgery
- ≥18 years, children under the age of 18 will be excluded due to rarity of disease
- Physician's clearance to participate in moderate-vigorous intensity exercise
- Able to read, write, and understand English
- Ability to understand and the willingness to sign an informed consent document
- Willing to undergo two venous blood draws for the study
Exclusion Criteria:
- Pre-existing musculoskeletal, neurological, or cardiorespiratory conditions, as
determined by the treating oncologist
- Participants with uncontrolled intercurrent illness, as determined by the treating
oncologist
- Participants with psychiatric illness/social situations that would limit compliance
with study requirements, as determined by the treating oncologist
- Participants who have received prior chemotherapy for cancer treatment (e.g. taxanes
for breast cancer)