Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03244033 · ClinicalTrials.gov registry record · NA

Integrating Contextual Factors Into Clinical Decision Support

A NA study, sponsored by University of Illinois at Chicago.

Completed
Registry status
NA
Development phase
452
Enrollment target

NCT03244033: Completed NA study, sponsored by University of Illinois at Chicago.

NCT03244033 is a NA study that has completed, run by University of Illinois at Chicago. The registered enrollment target is 452 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03244033, a NA study, has completed, sponsored by University of Illinois at Chicago.

COMPLETED
Registry status
NA
Development phase
452 participants
Enrollment target

Study Summary

Preventing contextual errors requires heightening clinician responsiveness to clues that there are contextual factors during the clinical encounter, in real time. These clues, termed contextual red flags are evident in two sources: the medical record and from patients directly. An effective intervention would prompt clinicians to determine whether there are underlying contextual factors that could be addressed in the care plan, averting contextual error. This desirable process is termed contextual probing. While clinical decision support (CDS) has been used to provide physicians with timely biomedical information at the point of care to prevent errors and promote appropriate care, this technology also affords an opportunity to draw physician attention to both contextual red flags and contextual factors in order to avert contextual errors. This study assesses the potential of "contextualized CDS" to improve contextualization of care through a randomized controlled intervention trial, with assessment measures of both patient health care outcomes and averted costs associated with overuse and misuse of medical services. The three hypotheses are that CDS: 1. Reduces contextual error: CDS tools that inform clinicians of contextual factors and prompt them to explore contextual red flags should result in a reduction in contextual error. 2. Improve health care outcomes: Contextualized CDS predicts improved health care outcomes defined as a partial or full resolution of the contextual red flag (e.g. elevated HgB A1c) after the index visit. 3. Reduces avoidable health care costs: Contextualized CDS is associated with a reduction in misuse and overuse of inappropriate or unnecessary medical services.

Primary Outcome

Proportion of red flags noted at index visit that have resolved

Interventions

  • OTHER Contextual clinical decision support
  • BEHAVIORAL Contextual survey

Trial Details

FieldValue
Enrollment Target 452 participants
Start Date 2018-09-01
Est. Completion 2021-11-12
Phase NA
University of Illinois at Chicago

430 total trials

What the finished NCT03244033 record still lists

NCT03244033 is an interventional study that assigns participants to a tested intervention. The registered 452 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 (68% lower).

The record links to 0 conditions, and to 2 interventions - of which Contextual clinical decision support is the first listed.

NCT03244033 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03244033 about?

NCT03244033 is a clinical study titled "Integrating Contextual Factors Into Clinical Decision Support". Preventing contextual errors requires heightening clinician responsiveness to clues that there are contextual factors during the clinical encounter, in real time. These clues, termed contextual red flags are evident in two sources: the medical record and from patients directly. An effective interven...

What is the current status of trial NCT03244033?

This trial is currently completed. It is a NA study. The enrollment target is 452 participants. The study started on 2018-09-01. Estimated completion is 2021-11-12.

What interventions are being tested in trial NCT03244033?

The interventions under investigation include: Contextual clinical decision support (OTHER), Contextual survey (BEHAVIORAL).

Who is sponsoring clinical trial NCT03244033?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03244033's enrollment target sits among peer trials

452 225th of 2000 higher than 1,776 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05676255 · 452 participants · Phase 2

    The Breast Cancer Survivors and Partners Online Research Together (SUPORT) Project

  • NCT05703178 · 452 participants · Phase 3

    Web-based Pain Coping Skills Training for Breast Cancer Survivors With AI-Associated Arthralgia

  • NCT03460977 · 453 participants · Phase 1

    A Study of Mevrometostat for Treatment of Relapsed/Refractory SCLC, Castration Resistant Prostate Cancer, and Follicular Lymphoma

  • NCT04708171 · 453 participants

    The PROGRAM-study: Awake Mapping Versus Asleep Mapping Versus No Mapping for Glioblastoma Resections

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03244033, the US trial registry maintained by the National Library of Medicine. NCT03244033 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.