Status:
COMPLETED
Study of Birth Control Use After Childbirth
Lead Sponsor:
WakeMed Health and Hospitals
Collaborating Sponsors:
University of North Carolina, Chapel Hill
Conditions:
Contraception
Eligibility:
FEMALE
14-45 years
Phase:
NA
Brief Summary
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-minu...
Eligibility Criteria
Inclusion
- 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
Exclusion
- 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
Key Trial Info
Start Date :
May 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2012
Estimated Enrollment :
800 Patients enrolled
Trial Details
Trial ID
NCT01443533
Start Date
May 1 2011
End Date
May 1 2012
Last Update
June 28 2012
Active Locations (1)
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1
WakeMed Hospital
Raleigh, North Carolina, United States, 27610