OCRA Distress & Unmet Needs Study for Gynecologic Cancer

This study is looking at the challenges faced by caregivers of people with gynecologic cancer. It aims to understand the distress and unmet needs of these caregivers, and how these factors might affect the patient's well-being. The study will use surveys to gather information from caregivers and patients over a 6-month period. Researchers will also explore a system designed to help caregivers find resources and support. The main goal is to see if this system can reduce caregiver distress and improve their access to needed resources. You may be able to join if you are 18 or older, speak English or Spanish, and have internet or phone access. The study is currently unclear on its recruitment status.

Study design
This is a prospective longitudinal cohort study with an embedded intervention, following participants over 6 months. It plans to enroll 250 participants.
What's involved
You would complete study surveys, primarily online, or with assistance from a coordinator via mail, phone, or tablet during clinic visits.
Compensation
Not stated in the trial record.
Follow-up
Safety and Adverse Events (AEs) will be measured through study completion, an average of 1 year.

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NCT07591623

OCRA Distress & Unmet Needs

Not Yet Recruiting
NAAges 18+InterventionalScreening
M.D. Anderson Cancer Center
~250 participants
Updated 2026-05-18 on ClinicalTrials.gov
What's tested:Surveys

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and Adverse Events (AEs)
Measured over Through study completion; an average of 1 year
Gynecologic Cancer
1 sites across 1 states
Texas1
  • Abigail Smith Zamorano, MD · PRINCIPAL_INVESTIGATOR · UT MD Anderson

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  • Safety and Adverse Events (AEs)Through study completion; an average of 1 year

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0