This is a prospective randomized control trial in which we propose an intervention in the immediate post-partum period to educate women about contraceptive options, particularly long acting reversible contraception (LARC) methods with an aim of increasing the amount of women who choose a LARC method.
Eligible participants will be identified in the post-partum period and will be randomized to one of two groups. The control group will receive the standard of care contraceptive counseling which includes any prenatal counseling they received as well as information from the nurse practitioner that rounds on them in the post-partum period. The intervention group will also receive the standard of care contraceptive counseling but will also watch a 10 minute video created by the CHOICE project which counsels on different contraceptive options. Both groups will fill out a pre-intervention questionnaire as well as a post-intervention questionnaire 24hrs later. The primary outcome will be which type of contraception each woman chooses. The secondary outcomes will include determining if the women come to their post-partum visits as well as if they get the method of contraception they chose on the post-partum floor.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
179
see intervention description
University Hospitals Case Medical Center
Cleveland, Ohio, United States
Choice of contraceptive method
Will be obtained through use of a questionnaire.
Time frame: 24 hours post-intervention
Return to clinic for postpartum visit
Will use ambulatory electronic medical record (EMR) to determine if patient returned to clinic for follow up visit.
Time frame: 12 weeks post-intervention
Obtained desired method of contraception
Will use ambulatory EMR to determine if patient received her desired method of contraception.
Time frame: 12 weeks post-intervention
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.