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NCT01990001 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by Medical University of South Carolina.

Completed
Registry status
NA
Development phase
118
Enrollment target

NCT01990001: Completed NA study, sponsored by Medical University of South Carolina.

NCT01990001 is a NA study that has completed, run by Medical University of South Carolina. The registered enrollment target is 118 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01990001, a NA study, has completed, sponsored by Medical University of South Carolina.

COMPLETED
Registry status
NA
Development phase
118 participants
Enrollment target

Study 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.

Primary Outcome

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. The primary outcome, which is proportion of reminder users, will be assessed three months after enrollment

Interventions

  • OTHER enrollment in online reminder system

Trial Details

FieldValue
Enrollment Target 118 participants
Start Date 2012-08
Est. Completion 2014-08
Phase NA

What the finished NCT01990001 record still lists

NCT01990001 is an interventional study that assigns participants to a tested intervention. The registered 118 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which enrollment in online reminder system is the first listed.

NCT01990001 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01990001 about?

NCT01990001 is a clinical study titled "Randomized Trial of Provider-Assisted Versus Patient-Initiated Enrollment in the Bedsider.Org Online Contraceptive Reminder Tool". 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 practi...

What is the current status of trial NCT01990001?

This trial is currently completed. It is a NA study. The enrollment target is 118 participants. The study started on 2012-08. Estimated completion is 2014-08.

What interventions are being tested in trial NCT01990001?

The interventions under investigation include: enrollment in online reminder system (OTHER).

Who is sponsoring clinical trial NCT01990001?

This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01990001's enrollment target sits among peer trials

118 803rd of 2000 higher than 1,194 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01990001, the US trial registry maintained by the National Library of Medicine. NCT01990001 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.