Clinical trial · Observational
Patient Related Outcomes for Gynecologic Radiation Oncology
LCCC 2052: Patient Related Outcomes for Gynecologic Radiation Oncology (PRO-GRO)
NCT04753086CI-TRIAL-00110296PRO-GROactive not recruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gynecologic Cancer | Malignant Female Reproductive System Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (1)
- label
- Gynecologic Cancer Pts
- description
- Gynecologic cancer patients being treated with radiation at UNC.
Primary outcomes (1)
- measure
- Rate of survey completion at acute timepoints
- timeFrame
- First week of radiation to 6 weeks after completing radiation
- description
- Percentage of patients who complete at least 75% of the questionnaires given after the baseline and up to and including the 6-week post-treatment survey
Secondary outcomes (26)
- measure
- Rate of survey completion at late timepoints
- timeFrame
- 6 months post-treatment to 2 years post-treatment
- description
- Percentage of patients who complete at least 75% of the questionnaires given after and including the 6-month post-treatment survey and up to and including the 2-year post-treatment survey
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
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)
References
Publications (0)
Data not yet available
No reference posted for this study.