Online Registry Improves Cancer Study Participation
Cedars-Sinai announced that its Research for Her online registry that matches women with research studies and clinical trials.
Cedars-Sinai announced that its Research for Her online registry that matches women with research studies and clinical trials, enrolled study participants more quickly when compared with traditional paper-based registries. A total of 322 women were enrolled in the Cedars-Sinai Research for Her registry over a 14-month period - a 4.3 fold increase over the paper-based registry. Of these 322 women, 263 were matched to at least one study and of those, 39 eligible individuals went on to enroll. The enrollment process increased in speed by 27 percent.
The Research for Her registry also spurred a 50 percent increase in enrollments for the Gilda Radner Hereditary Cancer Program, part of the Women's Cancer Program at the Cedars-Sinai Samuel Oschin Comprehensive Cancer Institute, in 2014. Research for Her, created in 2013, is currently open to all women over the age of 18 with or without a prior history of cancer. It soon will expand to also enroll and link men to available clinical trials or research studies at Cedars-Sinai.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
