Study of Birth Control Use After Childbirth
Completed · Not applicable
Conditions studied: Contraception
In brief
This study is a randomized controlled trial that will evaluate the impact of a brief educational script on the method of birth control that women receive at their 6-week postpartum visit. The one-minute script ("LARC script") is given to women in the hospital during their postpartum admission. It informs patients about long-acting reversible contraceptive (LARC) methods, specifically the contraceptive implant and the intrauterine device. The investigators hypothesize that women who are randomized to receive the LARC script will be more likely to report that they are using a LARC method, when queried immediately after their six-week postpartum visit.
Key facts
- Study ID
- NCT01443533
- Run by
- WakeMed Health and Hospitals
- People needed
- 800
- Starts
- 2011-05-01
- Expected to finish
- 2012-05-01
- Last updated by the study team
- 2012-06-28
Who can join
Age: 14 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Women who are admitted to the postpartum unit at WakeMed Hospital
- Delivery of a live infant >24 weeks gestational age
- Age 14-45 years
- Ability to speak either English or Spanish fluently
- Willing to be contacted by phone until at least 8 weeks after delivery
You may not qualify if…
- History of a tubal ligation or hysterectomy
- Partner has already had a vasectomy
- History of fertility treatment to conceive this pregnancy
- Previous randomization into the study
Where it is running
- WakeMed Hospital — Raleigh, North Carolina, United States
Full record on ClinicalTrials.gov
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