Young, Black, or uninsured women were more likely to participate in a randomized trial.
Enrollment of diverse populations into clinical trials is critical to ensure generalizability of outcomes and to avoid bias. Investigators examined the rates and reasons for declining to enroll in a trial that compared induction at 39 weeks with expectant management in low-risk, nulliparous women.
In all, 28% of eligible women consented to enroll in this multicenter, NIH-sponsored trial. Women who were Black (versus white; odds ratio, 1.5), without private insurance (OR, 1.6), and younger than 29 years were more likely to consent. Asian women were less likely to consent, often citing a preference for expectant management, unwillingness to participate in research, and objections from friends and family, as their reasons.
Reviewing Author
DisclosuresConsultant/Advisory BoardAicuris; Bayer; GSK; Innovative Molecules; Merck; MAPP Biopharmaceutical (Safety Monitoring Committee)
RoyaltiesUpToDate
Grant/Research SupportNIH/National Institute of Allergy and Infectious Diseases; GSK; Moderna; Assembly Biomedical; Aicuris
Editorial BoardsSexually Transmitted Diseases; Sexually Transmitted Infections; Journal of Infectious Diseases
Leadership PositionsID Division Chiefs Community of Practice (At-Large Member)
DisclosuresConsultant/Advisory BoardAicuris; Bayer; GSK; Innovative Molecules; Merck; MAPP Biopharmaceutical (Safety Monitoring Committee)
RoyaltiesUpToDate
Grant/Research SupportNIH/National Institute of Allergy and Infectious Diseases; GSK; Moderna; Assembly Biomedical; Aicuris
Editorial BoardsSexually Transmitted Diseases; Sexually Transmitted Infections; Journal of Infectious Diseases
Leadership PositionsID Division Chiefs Community of Practice (At-Large Member)