Trial · NCT04181307
A Randomized Trial of a BE-EHR Module to Guide the Care of Older Adults With Diabetes
NCT04181307, Not applicable, Completed, NYU Langone Health; results first posted 2023-07-19
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. A Randomized Trial of a BE-EHR Module to Guide the Care of Older Adults With Diabetes. Trials, record NCT04181307. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04181307
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- A Randomized Trial of a BE-EHR Module to Guide the Care of Older Adults With Diabetes
- NCT number
- NCT04181307
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 7,630 participants, actual
- Lead sponsor
- NYU Langone Health
- Conditions
- Diabetes
- Interventions
- BE-EHR module
- First posted
- 2019-11-29
- Last updated
- 2023-07-19
- Results first posted
- 2023-07-19
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants Who Are CW-Compliant and CW-Noncompliant | Month 18 | In order to evaluate Choosing Wisely (CW) compliance status, the BE-EHR algorithm will capture information on demographics, diagnoses in the patient's problem list, prescription history, and relevant lab results (i.e. allergies and blood glucose (HbA1c)) The study team members will not collect this information directly; data will be collected in NYULH's EHR system, EPIC, and an EPIC Reporting analyst will extract the relevant parameters from the EHR into a report. The study team members only receive the ultimate determination from the algorithm that the patient is either CW-compliant or CW-noncompliant. |
| Secondary | Number of Total Prescription Encounters | Month 18 | The Refill Protocol nudge activates in Epic any time a medication refill for either Metformin or a non-Metformin diabetes medication is generated for a patient over 75 |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants Who Are CW-Compliant and CW-Noncompliant | Month 18 | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Number of Total Prescription Encounters | Month 18 | Prescription Encounters | NUMBER |
Source ClinicalTrials.gov
Results by group6
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants Who Are CW-Compliant and CW-Noncompliant | Standard EPIC Instantiation | CW-Compliant | 412 | Participants | |
| Number of Participants Who Are CW-Compliant and CW-Noncompliant | Standard EPIC Instantiation Plus the BE-EHR Module. | CW-Compliant | 704 | Participants | |
| Number of Participants Who Are CW-Compliant and CW-Noncompliant | Standard EPIC Instantiation | CW-Noncompliant | 1232 | Participants | |
| Number of Participants Who Are CW-Compliant and CW-Noncompliant | Standard EPIC Instantiation Plus the BE-EHR Module. | CW-Noncompliant | 1854 | Participants | |
| Number of Total Prescription Encounters | Standard EPIC Instantiation | 0 | Prescription Encounters | ||
| Number of Total Prescription Encounters | Standard EPIC Instantiation Plus the BE-EHR Module. | 2056 | Prescription Encounters |
Source ClinicalTrials.gov
Participant flow10
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Standard EPIC Instantiation | 2,986 | |
| Overall Study | STARTED | Standard EPIC Instantiation Plus the BE-EHR Module. | 4,644 | |
| Overall Study | Assessed at Baseline | Standard EPIC Instantiation | 1,342 | |
| Overall Study | Assessed at Baseline | Standard EPIC Instantiation Plus the BE-EHR Module. | 2,086 | |
| Overall Study | Assessed at 18 Months | Standard EPIC Instantiation | 1,644 | |
| Overall Study | Assessed at 18 Months | Standard EPIC Instantiation Plus the BE-EHR Module. | 2,558 | |
| Overall Study | COMPLETED | Standard EPIC Instantiation | 1,342 | |
| Overall Study | COMPLETED | Standard EPIC Instantiation Plus the BE-EHR Module. | 2,086 | |
| Overall Study | NOT COMPLETED | Standard EPIC Instantiation | 1,644 | |
| Overall Study | NOT COMPLETED | Standard EPIC Instantiation Plus the BE-EHR Module. | 2,558 |
Source ClinicalTrials.gov
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Standard EPIC Instantiation | 18 | 1,644 |
| Total, all-cause mortality | Standard EPIC Instantiation Plus the BE-EHR Module. | 21 | 2,558 |
| Total, other adverse events | Standard EPIC Instantiation | 0 | 1,644 |
| Total, other adverse events | Standard EPIC Instantiation Plus the BE-EHR Module. | 0 | 2,558 |
| Total, serious adverse events | Standard EPIC Instantiation | 0 | 1,644 |
| Total, serious adverse events | Standard EPIC Instantiation Plus the BE-EHR Module. | 0 | 2,558 |
Source ClinicalTrials.gov
Papers3
The papers the trial lists on ClinicalTrials.gov.
Grants1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years |
|---|---|---|---|---|---|
| R33AG057382 | EHR nudges: Development and testing of a behavioral economics electronic health record module | TROXEL, ANDREA B; MANN, DEVIN M | NEW YORK UNIVERSITY SCHOOL OF MEDICINE | NATIONAL INSTITUTE ON AGING | 2019 to 2021 |
Source NIH RePORTER
Trial comparisons2
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Standard EPIC Instantiation vs Standard EPIC Instantiation Plus the BE-EHR Module.: deaths from any cause | Trial comparisons |
| Standard EPIC Instantiation vs Standard EPIC Instantiation Plus the BE-EHR Module.: serious adverse events | Trial comparisons |
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04181307
GET https://conductscience.org/api/trials/v1/NCT04181307/registered