Randomized Trial of Provider-Assisted Versus Patient-Initiated Enrollment in the Bedsider.Org Online Contraceptive Reminder Tool

Completed · Not applicable

Conditions studied: Contraceptive Adherence and Continuation

In brief

The broad objective of this research is to determine whether a quick, simple intervention will increase utilization of contraceptive reminders and adherence to short-term contraceptive regimens. Such an intervention could be implemented easily with no additional resources into a busy clinical practice.

Key facts

Study ID

NCT01990001

Run by

Medical University of South Carolina

People needed

118

Starts

2012-08-01

Expected to finish

2014-08-01

Last updated by the study team

2015-09-23

Who can join

Age: 18 and older, up to 29. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Female, 18-29 years old
• Prescribed one of the following birth control:
• Oral contraceptive pills, vaginal ring, transdermal patch, or Depo Provera
• Able to provide consent
• Have regular access to a computer, Ipad, or a hand-held device such as a smartphone.
• Women must be able to read and speak English(Bedsider website in not translated into Spanish)

You may not qualify if…

• Male
• Over the age of 30 years old
• Non-English Speaking
• Limited or no access to computer, Ipad or hand-held device(smartphone)

Where it is running

• MUSC Women's Health- Cannon — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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