Status:
UNKNOWN
Use of an Educational Multimedia Tool Versus Routine Care for the Uptake of Postpartum LARC in High-Risk Pregnancies
Lead Sponsor:
The University of Texas Health Science Center, Houston
Collaborating Sponsors:
Merck Sharp & Dohme LLC
Conditions:
Pregnancy, High Risk
Contraception
Eligibility:
FEMALE
13-50 years
Phase:
NA
Brief Summary
The purpose of the study is to evaluate if the implementation of a multimedia based educational tool and regular reminders with shared decision-making will increase the rate of LARC uptake and retenti...
Detailed Description
This study will include 380 women aged 18-50 enrolled between 28 weeks gestation and postpartum day #1 who have a pregnancy that is considered high-risk. After consent, participants will be randomized...
Eligibility Criteria
Inclusion
- Aged 13-50 years old
- High risk pregnancy due to either maternal medical conditions or obstetric/neonatal complications
Exclusion
- Planned cesarean hysterectomy
- Unable to provide informed consent in either English or Spanish
- Unable to provide reliable cell phone access for the study duration
- Not willing to provide follow-up for two years
Key Trial Info
Start Date :
July 9 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 30 2023
Estimated Enrollment :
380 Patients enrolled
Trial Details
Trial ID
NCT04291040
Start Date
July 9 2020
End Date
January 30 2023
Last Update
November 14 2022
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030