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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01990001
Enrollment
118
Registered
2013-11-21
Start date
2012-08-31
Completion date
2014-08-31
Last updated
2015-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contraceptive Adherence and Continuation

Keywords

contraception, adherence, medication reminder

Brief summary

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.

Detailed description

The specific aims of the study are to: 1. Measure the difference in reminder utilization over three months between patients who are assisted with initiating the reminder system during their office visit versus those who are encouraged to self-initiate after the visit. 2. Assess whether provider-assisted enrollment in the online reminder system improves adherence to a short-term contraceptive regimen compared to self- initiated enrollment after the visit.

Interventions

OTHERenrollment in online reminder system

Study personnel enrolled members in the online reminder system during their office visit.

Sponsors

American College of Obstetricians and Gynecologists
CollaboratorOTHER
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 29 Years
Healthy volunteers
Yes

Inclusion criteria

1. Female, 18-29 years old 2. Prescribed one of the following birth control: Oral contraceptive pills, vaginal ring, transdermal patch, or Depo Provera 3. Able to provide consent 4. Have regular access to a computer, Ipad, or a hand-held device such as a smartphone. 5. Women must be able to read and speak English(Bedsider website in not translated into Spanish)

Exclusion criteria

1. Male 2. Over the age of 30 years old 3. Non-English Speaking 4. Limited or no access to computer, Ipad or hand-held device(smartphone)

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients using the online reminder tool three months after enrollment3 monthsMeasure the difference in reminder utilization over three months between patients who are assisted with initiating the reminder system during their office visit versus those who are encouraged to self-initiate after the visit. The primary outcome, which is proportion of reminder users, will be assessed three months after enrollment

Secondary

MeasureTime frameDescription
Assess whether provider-assisted enrollment in the online reminder system improves adherence to a short-term contraceptive regimen compared to self- initiated enrollment after the visit.3 monthsAssess whether provider-assisted enrollment in the online reminder system improves adherence to a short-term contraceptive regimen compared to self- initiated enrollment after the visit. This data will be collected three months after enrollment

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026