Contraceptive Counseling in the Postpartum Period



Status:Recruiting
Healthy:No
Age Range:18 - Any
Updated:5/3/2017
Start Date:March 2015
End Date:October 2017
Contact:Ali McGregor, MD
Email:ali.mcgregor@uhhospitals.org
Phone:2168441000

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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.

Inclusion Criteria:

- Women giving birth at University Hospitals Case Medical Center

- Patient of the Women's Health Center

- Women delivering only one child

- Women receiving contraceptive counseling from the nurse practitioner that cares for
the postpartum unit

Exclusion Criteria:

- Severe neonatal complication at time of delivery (neonatal death, neonatal admission
to the neonatal intensive care unit (NICU) except in cases of chorioamnionitis)

- Severe maternal complication at time of delivery (patient requiring intensive care
unit care, patient requiring hysterectomy at time of delivery)

- Preterm delivery <34 weeks
We found this trial at
1
site
Cleveland, Ohio 44194
Phone: 216-844-1000
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mi
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Cleveland, OH
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