Video Counseling for Effective Postpartum Contraception
| Status: | Recruiting |
|---|---|
| Conditions: | Contraception, Contraception |
| Therapuetic Areas: | Reproductive |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 4/21/2016 |
| Start Date: | May 2015 |
| End Date: | May 2016 |
| Contact: | Jessica Morse, MD |
| Email: | jessica_morse@med.unc.edu |
| Phone: | 919-843-8028 |
Video Counseling for Effective Postpartum Contraception: a Randomized Clinical Trial
This is a randomized clinical trial to evaluate if the addition of long-acting reversible
contraception (LARC) focused video-counseling during prenatal care increases uptake of
postpartum LARC.
contraception (LARC) focused video-counseling during prenatal care increases uptake of
postpartum LARC.
Eligible participants will be identified in the prenatal period and will be randomized to
one of two groups. The control group will receive the standard of care contraceptive
counseling during prenatal counseling. The intervention group will also receive the standard
of care contraceptive counseling during prenatal care, but will also watch an
evidence-based,12 minute LARC First video created by the CHOICE project which provides
information on different contraceptive methods. All participants will receive information
regarding access to free LARC methods in the postpartum period. All participants will be
called at 12 weeks postpartum. Independent of randomization arm, they will all undergo a
5-minute survey by phone about contraceptive method choice and use.
one of two groups. The control group will receive the standard of care contraceptive
counseling during prenatal counseling. The intervention group will also receive the standard
of care contraceptive counseling during prenatal care, but will also watch an
evidence-based,12 minute LARC First video created by the CHOICE project which provides
information on different contraceptive methods. All participants will receive information
regarding access to free LARC methods in the postpartum period. All participants will be
called at 12 weeks postpartum. Independent of randomization arm, they will all undergo a
5-minute survey by phone about contraceptive method choice and use.
Inclusion Criteria:
- woman presenting for routine prenatal care visit at University of North Carolina
(UNC) Resident Continuity Clinic
- least 18 years old
- fluent in English
- able to read to a third-grade reading level
- not planning sterilization for postpartum contraception
- at least 28 weeks gestation at time of enrollment
Exclusion Criteria:
- those who do not meet the previously outlined inclusion criteria
- those who are unable to provide informed consent.
We found this trial at
1
site
101 Manning Drive
Chapel Hill, North Carolina 27599
Chapel Hill, North Carolina 27599
Phone: 919-962-5299
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