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NCT04829188 · ClinicalTrials.gov registry record · NA

Comparative Effectiveness of Readmission Reduction Interventions for Individuals with Sepsis or Pneumonia

A NA study, sponsored by University of Pittsburgh.

Completed
Registry status
NA
Development phase
1,288
Enrollment target

NCT04829188 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 1,288 participants.

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The verdict

NCT04829188, a NA study, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
NA
Development phase
1,288 participants
Enrollment target

Study Summary

An adaptive platform trial to compare effectiveness of different care models to prevent readmissions for patients hospitalized with sepsis or lower respiratory tract infection. The primary outcome is number of days spent at home within 90 days after hospital discharge.

Interventions

  • BEHAVIORAL Structured Telephone Support (STS)
  • BEHAVIORAL Low-intensity Remote Patient Monitoring (RPM-Low)
  • BEHAVIORAL High-intensity Remote Patient Monitoring (RPM-High)
  • BEHAVIORAL Standard Response Team
  • BEHAVIORAL Enhanced Response Team

Trial Details

FieldValue
Enrollment Target 1,288 participants
Start Date 2021-03-30
Est. Completion 2024-12-15
Phase NA

Sponsor

University of Pittsburgh

1,238 total trials

What the Registry Record Tells You About NCT04829188

The ClinicalTrials.gov registry entry for NCT04829188 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,288 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 5 interventions - of which Structured Telephone Support (STS) is the first listed.

NCT04829188 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04829188 about?

NCT04829188 is a clinical study titled "Comparative Effectiveness of Readmission Reduction Interventions for Individuals with Sepsis or Pneumonia". An adaptive platform trial to compare effectiveness of different care models to prevent readmissions for patients hospitalized with sepsis or lower respiratory tract infection. The primary outcome is number of days spent at home within 90 days after hospital discharge.

What is the current status of trial NCT04829188?

This trial is currently completed. It is a NA study. The enrollment target is 1,288 participants. The study started on 2021-03-30. Estimated completion is 2024-12-15.

What interventions are being tested in trial NCT04829188?

The interventions under investigation include: Structured Telephone Support (STS) (BEHAVIORAL), Low-intensity Remote Patient Monitoring (RPM-Low) (BEHAVIORAL), High-intensity Remote Patient Monitoring (RPM-High) (BEHAVIORAL), Standard Response Team (BEHAVIORAL), Enhanced Response Team (BEHAVIORAL).

Who is sponsoring clinical trial NCT04829188?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.