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NCT04294901 · ClinicalTrials.gov registry record · NA
Engaging Patients to Promote Deprescribing
A NA study of Deprescriptions and Medical Overuse, sponsored by VA Office of Research and Development.
- Completed
- Registry status
- NA
- Development phase
- 5,946
- Enrollment target
- 4
- Study locations
NCT04294901: Completed NA study of Deprescriptions and Medical Overuse, sponsored by VA Office of Research and Development.
NCT04294901 is a NA study of Deprescriptions and Medical Overuse that has completed, run by VA Office of Research and Development. The registered enrollment target is 5,946 participants, above the 1,403-participant average among 58,714 other NA trials with a reported enrollment target (324% higher). The trial reports 4 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04294901, a NA study of Deprescriptions and Medical Overuse, has completed, sponsored by VA Office of Research and Development.
- COMPLETED
- Registry status
- NA
- Development phase
- 5,946 participants
- Enrollment target
- 4
- Study locations
Study Summary
One mechanism to reduce potentially inappropriate medications is through deprescribing, a deimplementation-based approach to thoughtfully discontinue a medication a patient is currently prescribed. Many interventions to overcome deprescribing barriers target the provider, who is already overburdened. Although some believe providers have primary responsibility for deprescribing, patient-initiated discontinuation discussions can effectively facilitate deprescribing. In a single-site pilot study, the investigators successfully engaged VA Primary Care patients to facilitate deprescribing of select potentially inappropriate medications. The investigators now propose a multisite randomized controlled trial of engaging Veterans who may be deprescribing candidates. By study end, the investigators will have established the effectiveness of an innovative, low-tech, patient-focused intervention to promote deprescribing, thereby directly improving quality, safety, and value of VA care while also setting the stage for generalization of this approach to other potentially inappropriate medications.
Primary Outcome
Non-refill of the medication in the 6 months following the primary care appointment (i.e., cessation) or any reduction in the total daily dose (i.e., de-escalation). There is an exception to the de-escalation rule for insulin, where only complete cessation will qualify since dose changes are less likely to be reflected in the order compared to oral medications.
Conditions Studied
Interventions
- BEHAVIORAL Direct to patient medication brochure
Study Locations (4)
Massachusetts
- VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA - Boston
- VA Central Western Massachusetts Healthcare System, Leeds, MA - Leeds
California
- San Francisco VA Medical Center, San Francisco, CA - San Francisco
New York
- James J. Peters VA Medical Center, Bronx, NY - The Bronx
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5,946 participants |
| Start Date | 2021-03-29 |
| Est. Completion | 2023-10-07 |
| Phase | NA |
What the finished NCT04294901 record still lists
NCT04294901 is an interventional study that assigns participants to a tested intervention. Its 5,946 participants enrollment target places it among the larger protocols in the corpus, above the 1,403-participant average among 58,714 other NA trials with a reported enrollment target (324% higher).
The record links to 3 conditions, with Deprescriptions appearing as the primary indexed condition, and to 1 intervention - of which Direct to patient medication brochure is the first listed.
NCT04294901 reports a single indexed study location in Massachusetts, California, New York.
Frequently Asked Questions
What is clinical trial NCT04294901 about?
NCT04294901 is a clinical study titled "Engaging Patients to Promote Deprescribing". One mechanism to reduce potentially inappropriate medications is through deprescribing, a deimplementation-based approach to thoughtfully discontinue a medication a patient is currently prescribed. Many interventions to overcome deprescribing barriers target the provider, who is already overburdened...
What is the current status of trial NCT04294901?
This trial is currently completed. It is a NA study. The enrollment target is 5,946 participants. The study started on 2021-03-29. Estimated completion is 2023-10-07.
What conditions does trial NCT04294901 study?
This clinical trial studies the following conditions: Deprescriptions, Medical Overuse, Inappropriate Prescribing.
What interventions are being tested in trial NCT04294901?
The interventions under investigation include: Direct to patient medication brochure (BEHAVIORAL).
Who is sponsoring clinical trial NCT04294901?
This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04294901 being conducted?
This trial has 4 study locations across California, Massachusetts, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT04294901's enrollment target sits among peer trials
5,946 24th of 2000 higher than 1,977 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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