Effect of Outpatient Symptom Management on Gynecologic Oncology Patients Receiving Chemotherapy
Uterine Cervical Neoplasms, Ovarian Neoplasms, Gynecologic Neoplasms
About this trial
This is an interventional supportive care trial for Uterine Cervical Neoplasms focused on measuring Palliative Care, Triage, Symptom Evaluation, Chemotherapy, Patient Distress
Eligibility Criteria
Inclusion Criteria:
- Female
- 18 years of age or older
- Diagnosis of Stage III, IV, or recurrent gynecologic malignancy (Uterine, Ovarian, Cervical, Vulvar, Vaginal, Fallopian Tube, Primary Peritoneal)
- Receiving active intravenous, intraperitoneal, or oral chemotherapy
- Patient at University of Michigan Gynecologic Oncology Clinic
Exclusion Criteria:
- Male
- Less than 18 years of age
- Patients without a diagnosis of a gynecologic malignancy
- Patients not receiving intravenous, intraperitoneal or oral chemotherapy at the time of enrollment
- Patients receiving radiation therapy with chemo-sensitization.
Sites / Locations
- University of Michigan Comprehensive Cancer Center
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Standard of Care
Symptom Management and Supportive Care
Patients randomized to this arm receive standard symptom management care by their primary gynecologic oncologist and complete the NCCN distress thermometer and ESAS-r at each visit, every 3-4 weeks.
Patients randomized to this arm are referred to a specialized symptom management and supportive care clinic and seen within two weeks. Patients will be seen in follow-up as recommended by the symptom management providers, and at each visit they will complete the ESAS-r and NCCN distress thermometer and return their responses either in person or by mail to the study team in a pre-addressed postage paid envelope.