Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Duke University
Eligible patients include women diagnosed with platinum-resistant ovarian cancer or recurrent ovarian cancer cancer. All patient participants will complete two quality of life (QOL) questionnaires and a cost-diary documenting their health care experience at time of consent and every 12 weeks thereafter. Consenting care givers will also be asked to complete two questionnaires to asses the impact of structured palliative care on them every 12 weeks.
Patients will be assigned to two arms randomly: 1) usual care or 2) structured palliative care. The primary endpoint is quality of life. A two-sided Chi-square test will be used to compare the proportion of patients who have improved quality of life after treatment between control arm and intervention arm. The average value of multiple scores after treatment will be used to compare with the baseline score before treatment for each question in the standard questionnaire.
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
You may be eligible if
Platinum-resistant ovarian cancer or recurrent ovarian cancer
Ability to read and respond to questions in English
You may not be if
Platinum-sensitive recurrent ovarian cancer without a significant clinical event
Existence of co-morbid disease, which in the opinion of the investigator prohibits participation in the protocol
