Leveraging EMR prompts to promote equitable clinical trial participation in gynecologic oncology: RE-AIM implementation results.
Abstract
e23294 Background: Lack of diversity and low enrollment limit clinical trial success in gynecologic oncology. Providers represent an underutilized resource for trial recruitment. Methods: At a single urban academic institution, gyn onc clinic note templates for new and return visits were modified to include a clinical trial screening prompt (“This patient was considered for clinical trial:” yes/no). Implementation was guided by the RE-AIM framework. A retrospective pre- and post-implementation review evaluated provider screening and trial enrollment. Patients were identified using clinic location and ICD-10 codes for cervical, uterine, and ovarian cancers; all confirmed diagnoses were included. Collected variables included cancer status, age, sex, race/ethnicity, insurance, and provider type. Descriptive statistics summarized patient characteristics. Associations were assessed using Firth penalized logistic regression. Results: Screening increased significantly post-implementation (OR 3.63, 95% CI 1.92–7.12; p < 0.001). African American patients had higher odds than White patients (OR 3.88, 95% CI 1.28–19.1; p = 0.013), indicating improved equity. Screening was higher among recurrence visits versus at the time of new diagnoses (OR 7.22, 95% CI 3.74–14.0; p < 0.001) and lower among surveillance patients (OR 0.09, 95% CI 0.01–0.37; p < 0.001). Compared with ovarian cancer, cervical cancer had lower odds, while corpus uteri cancer showed no difference. Post-implementation, use of the tool was higher for new diagnoses (OR 1.71, 95% CI 1.08–2.71; p = 0.022) and recurrence (OR 4.53, 95% CI 2.27–9.34; p < 0.001) versus surveillance. Conclusions: EMR-based clinical trial prompts significantly increased screening in Gyn Onc clinics. Higher screening among African American patients suggests this low-cost intervention may reduce inequities. Variability by disease status and cancer type identifies targets for ongoing improvement. EMR-integrated prompts offer a scalable strategy to promote equitable trial access. Characteristic N Event N Event % OR 95% CI p-value Race/Ethnicity White 203 2 1.0% — — African American 706 32 4.5% 3.88 1.28, 19.11 0.013 Other 57 3 5.3% 5.18 0.98, 31.75 0.052 Hispanic 41 2 4.9% 5.10 0.77, 33.94 0.087 Unknown 20 2 10% 10.89 1.60, 74.47 0.018 Asian 16 0 0% 2.44 0.02, 31.70 0.606 Diagnosis Code C56.X: Malignant neoplasm of ovary 284 11 3.9% — — C54.X: Malignant neoplasm of corpus uteri 608 30 4.9% 1.25 0.64, 2.61 0.516 C53.X: Malignant neoplasm of cervix uteri 151 0 0% 0.08 0.00, 0.61 0.009 Cancer Status New diagnosis 526 19 3.6% — — Recurrence 98 21 21% 7.22 3.74, 14.04 <0.001 Surveillance 417 1 0.2% 0.09 0.01, 0.37 <0.001 Type of Insurance Private 430 18 4.2% — — Medicaid 156 5 3.2% 0.81 0.28, 2.01 0.664 Medicare 444 18 4.1% 0.97 0.50, 1.88 0.921 Self-pay 11 0 0% 0.97 0.01, 7.97 0.983 Other 2 0 0% 4.46 0.03, 57.45 0.418
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (7)
Jennifer Welch
11Hasbro Children's Hospital, Warren Alpert Medical School of Brown University, Division of Pediatric Hematology-Oncology, Providence, United States
Badr Abdullah
Georgetown University, Washington, DC
Reeda Iqbal
Georgetown University, Washington, DC
K. Nivana Theethira Poonacha
Georgetown University, Washington, DC
Kelsey Lyons
Georgetown University, Washington, DC
Serenity Budd
MedStar Health Research Institute, Washington, DC
Ebony Rashaan Hoskins
MedStar Washington Hospital Center, Washington, DC