OCRA Distress & Unmet Needs
ConditionGynecologic Cancer
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorM.D. Anderson Cancer Center
About this trial
This study is a prospective longitudinal cohort study with an embedded intervention. It follows participants with gynecologic malignancies and their informal caregivers over a 6-month period to assess caregiver distress, NMDOH, and patient outcomes.
Eligibility criteria
Qualifiers
Must be at least 18 years old
Must read and speak English or Spanish
Participants must have access to the internet via a smartphone, tablet, or computer (public or private), or have reliable access to a telephone to communicate with the study coordinator.
Patient presenting for initial or recurrence chemotherapy treatment for management of a gynecologic malignancy (cancer of the ovary, uterus, cervix, vulva, vagina, peritoneum, or fallopian tube)
Disqualifiers
None
Trial design
Treatments tested in this trial
- Surveys
Treatment groups
250 Participants
are divided into 2 treatment groupsSponsors and collaborators
M.D. Anderson Cancer Center
Lead sponsor
Ovarian Cancer Research Alliance (OCRA)
Collaborator
Source ClinicalTrials.gov