Improving Adolescent Adherence to Hormonal Contraception
Completed · Not applicable
Conditions studied: Contraception
In brief
The purpose of this study is to determine whether contraceptive compliance by young women can be improved through expanded counseling by a health educator at the initial clinic visit as compared with standard care.
Key facts
- Study ID
- NCT00584038
- Run by
- The University of Texas Medical Branch, Galveston
- People needed
- 1155
- Starts
- 2006-01-01
- Expected to finish
- 2012-03-01
- Last updated by the study team
- 2013-05-24
Who can join
Age: 16 and older, up to 24. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Sexually active females 16 to 24 years of age who present to a University of Texas Medical Branch (UTMB) clinic and request to initiate oral contraception for birth control.
You may not qualify if…
- Women who are currently pregnant or breastfeeding.
- Women who wish to become pregnant within the next 12 months.
- Women who have a medical contraindication to use of estrogen (e.g., thromboembolic disease, acute liver disease, breast cancer, genital cancer, or undiagnosed genital bleeding).
- Women wishing to initiate use of a contraceptive method that is not oral, such as transdermal (the patch) or injectable (DMPA) methods, or the vaginal ring.
- Current and previous users of oral contraceptives.
Where it is running
- The University of Texas Medical Branch — Galveston, Texas, United States
Full record on ClinicalTrials.gov
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