Debunking Myths About Contraceptive Safety Among Women in Kingston, Jamaica

The investigators will conduct a randomized trial (RT) of consenting adult women (N=220) to test the effectiveness of the final intervention video. Participants in the RT will complete the "Enrollment Questionnaire" and then will be randomized to either watch a short video on 1) debiasing about LARC safety (intervention arm; n=110) or 2) vector control (control arm; n=110) (Figure 2). Participants then will have the option of receiving routine contraceptive services that follow standard care. After three months, trained interviewers will contact participants to administer the short "Follow‐up Questionnaire" via telephone. To corroborate participant reporting of contraception use during follow‐up, the investigators also will extract data on LARC use from participant medical records.