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Active Not RecruitingNCT04753086

Patient Related Outcomes for Gynecologic Radiation Oncology

LCCC 2052: Patient Related Outcomes for Gynecologic Radiation Oncology (PRO-GRO)

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
100 (actual)
Sponsor
UNC Lineberger Comprehensive Cancer Center · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to see if it is feasible to use electronic questionnaires to measure patient related outcomes before, during, and after radiation for gynecologic cancer in a high-volume radiation oncology clinic.

Detailed description

Other studies have found benefits from using patient related outcome measurements (PROM) in clinical settings, and a paper PROM is part of standard of care treatment for prostate cancer patients at the University of North Carolina clinic. However, PROM are not routinely collected for gynecological cancer patients at UNC, and fewer studies have specifically focused on PROM for gynecological cancer patients receiving radiation. The primary objective of this study is to determine the feasibility of PRO monitoring of gynecologic symptoms before, during (at weekly intervals), and after radiation (external beam radiotherapy and brachytherapy) for gynecologic cancer patients at a high volume center.

Conditions

Timeline

Start date
2022-06-01
Primary completion
2026-04-01
Completion
2028-02-15
First posted
2021-02-15
Last updated
2026-01-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04753086. Inclusion in this directory is not an endorsement.

Patient Related Outcomes for Gynecologic Radiation Oncology (NCT04753086) · Clinical Trials Directory