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NCT00766207 · ClinicalTrials.gov registry record · NA
Electronic Notification of Teratogenic Risks
A NA study, sponsored by University of Pittsburgh.
- Completed
- Registry status
- NA
- Development phase
- 2,593
- Enrollment target
NCT00766207 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 2,593 participants.
The verdict
NCT00766207, a NA study, has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- NA
- Development phase
- 2,593 participants
- Enrollment target
Study Summary
This study will use a factorial design randomized controlled trial to (1)compare multi-faceted decision support (intervention) to streamlined clinical alerts (control) and (2) evaluate whether collecting information about women's risk of pregnancy using a networked tablet computer (intervention) is superior to the way clinicians usually collect this information (control). Over the course of 1 year, we will abstract data from the electronic medical record when study clinicians prescribe teratogenic medications, conduct phone interviews with women prescribed medications by participating clinicians, and survey participating clinicians about their satisfaction with the decision support they receive. We will use this data to confirm our hypotheses that clinicians in the intervention groups will (1) prescribe fewer teratogenic medications, (2) be more likely to prescribe contraception when a teratogenic medication is prescribed, (3) have more patients report satisfaction with the counseling they received, and (4) report more satisfaction with the decision support they received.
Interventions
- OTHER Clinical decision support
- OTHER stream-lined clinical alert
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,593 participants |
| Start Date | 2008-10 |
| Est. Completion | 2011-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00766207
The ClinicalTrials.gov registry entry for NCT00766207 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 2,593 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Clinical decision support is the first listed.
NCT00766207 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00766207 about?
NCT00766207 is a clinical study titled "Electronic Notification of Teratogenic Risks". This study will use a factorial design randomized controlled trial to (1)compare multi-faceted decision support (intervention) to streamlined clinical alerts (control) and (2) evaluate whether collecting information about women's risk of pregnancy using a networked tablet computer (intervention) is ...
What is the current status of trial NCT00766207?
This trial is currently completed. It is a NA study. The enrollment target is 2,593 participants. The study started on 2008-10. Estimated completion is 2011-05.
What interventions are being tested in trial NCT00766207?
The interventions under investigation include: Clinical decision support (OTHER), stream-lined clinical alert (OTHER).
Who is sponsoring clinical trial NCT00766207?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
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