Patient Related Outcomes for Gynecologic Radiation Oncology

RECRUITING

I'm interested ...!!

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.

Conditions:

🦠 Gynecologic Cancer

🗓️ Study Start (Actual) 1 June 2022

🗓️ Primary Completion (Estimated) 27 September 2024

✅ Study Completion (Estimated) 27 September 2026

👥 Enrollment (Estimated) 100

🔬 Study Type OBSERVATIONAL

📊 Phase N/A

Locations:

📍 Chapel Hill, North Carolina, United States

📋 Eligibility Criteria

Description

Inclusion Criteria:

* 18 years or older
* English speaking
* Informed consent reviewed and signed
* Gynecologic cancer being treated by radiation at UNC
* Able and willing to complete web-based symptom survey

Exclusion Criteria:

* Inability to read and speak English
* Current incarceration
* Pregnancy
* Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rending of informed consent (with the caveat that if they initially are hospitalized with delirium which is subsequently resolved, they can then be consented for participation at a later time)

Ages Eligible for Study: 18 Years to N/A (ADULT, OLDER_ADULT)

Sexes Eligible for Study: FEMALE

Accepts Healthy Volunteers: No

🗓️ Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

First Submitted 3 February 2021
First Submitted that Met QC Criteria 10 February 2021
First Posted 15 February 2021

Study Record Updates

Last Update Submitted that Met QC Criteria 17 January 2024
Last Update Posted 19 January 2024
Last Verified January 2024