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NCT02534987 · ClinicalTrials.gov registry record · NA

Integrated Clinical Prediction Rules: Bringing Evidence to Diverse Primary Care Settings

A NA study of Pneumonia and Strep Throat, sponsored by NYU Langone Health.

Completed
Registry status
NA
Development phase
33
Enrollment target
1
Study location

NCT02534987 is a NA study of Pneumonia and Strep Throat that has completed, run by NYU Langone Health. The registered enrollment target is 33 participants, below the 4,519-participant average among 47 other Pneumonia trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02534987, a NA study of Pneumonia and Strep Throat, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
NA
Development phase
33 participants
Enrollment target
1
Study location

Study Summary

The study is a randomized controlled trial, with an Intervention Group and a Control Group at the University of Utah (U of U) and University of Wisconsin (UW). BU serves as the primary award and coordinating institution. The unit of randomization will be at the clinic level at each institution. UW will recruit all General Internal Medicine (GIM) Clinics and Department of Family Medicine (DFM) Clinics in Dane County as well as their East and West Urgent Care Clinics. U of U will recruit all affiliated primary care practices. The unit of randomization will be the clinic. The study biostatistician will receive a list of clinic sites that have agreed to participate in the study from the site PIs. Clinics will be randomized to either Intervention group or to a Control group stratified by clinic size. Both groups will receive a single 45 minute academic detailing session describing evidenced-based diagnosis and treatment for strep throat and pneumonia. The Intervention Group will also receive a demonstration of the iCPR tool during their academic detailing session. Providers and clinic staff will be invited to the academic detailing session. Any provider or staff that is unable to attend the session will receive written and electronic copies of the material. Individual providers will not be specifically recruited for participation and they will participate or not based on personal preferences as they would for any clinic quality improvement project. The iCPR tool will be "turned on" for providers in the Intervention group. This means that the best practice alerts will trigger for appropriate patients with suspected strep throat or pneumonia. We will collect and analyze data about the use of each element of the iCPR tool during patient visits, including which elements of the tool were used and how often. We will also collect data from the site EHRs about antibiotic and diagnostic test orders for strep throat and pneumonia from all clinics participating in the trial, both

Conditions Studied

Interventions

  • OTHER iCPR2

Study Locations (1)

New York

  • New York University School of Medicine - New York

Trial Details

FieldValue
Enrollment Target 33 participants
Start Date 2015-03
Est. Completion 2018-06
Phase NA

Sponsor

NYU Langone Health

1,164 total trials

What the Registry Record Tells You About NCT02534987

The ClinicalTrials.gov registry entry for NCT02534987 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 33 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,519-participant average among 47 other Pneumonia trials with a reported enrollment target (99% lower). The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pneumonia appearing as the primary indexed condition, and to 1 intervention - of which iCPR2 is the first listed.

NCT02534987 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT02534987 about?

NCT02534987 is a clinical study titled "Integrated Clinical Prediction Rules: Bringing Evidence to Diverse Primary Care Settings". The study is a randomized controlled trial, with an Intervention Group and a Control Group at the University of Utah (U of U) and University of Wisconsin (UW). BU serves as the primary award and coordinating institution. The unit of randomization will be at the clinic level at each institution. UW w...

What is the current status of trial NCT02534987?

This trial is currently completed. It is a NA study. The enrollment target is 33 participants. The study started on 2015-03. Estimated completion is 2018-06.

What conditions does trial NCT02534987 study?

This clinical trial studies the following conditions: Pneumonia, Strep Throat.

What interventions are being tested in trial NCT02534987?

The interventions under investigation include: iCPR2 (OTHER).

Who is sponsoring clinical trial NCT02534987?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02534987 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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