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NCT04576065 · ClinicalTrials.gov registry record · NA

Wake Forest Post-ICU Telehealth (WFIT) Program

A NA study of Critical Illness, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
NA
Development phase
413
Enrollment target
1
Study location

NCT04576065 is a NA study of Critical Illness that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 413 participants, below the 3,134-participant average among 91 other Critical Illness trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04576065, a NA study of Critical Illness, has completed, sponsored by Wake Forest University Health Sciences.

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

Study Summary

Wake Forest Post-Intensive Care Unit Telehealth (WFIT) program consists of a nurse practitioner who has access to daily activity data as well as telehealth capabilities for 6 months post-hospital discharge in order to improve the post-critical illness care of patients. The study team expects that this program will reduce costs to patients. Through this intervention the study team hopes to improve quality of life, patient satisfaction, reduce readmissions and ER visits, and reduce mortality. The study team will perform a formal randomized controlled trial with a cost-effectiveness analysis to demonstrate its value.

Conditions Studied

Interventions

  • OTHER WFIT

Study Locations (1)

North Carolina

  • Wake Forest University Health Sciences - Winston-Salem

Trial Details

FieldValue
Enrollment Target 413 participants
Start Date 2021-03-19
Est. Completion 2023-09-14
Phase NA

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT04576065

The ClinicalTrials.gov registry entry for NCT04576065 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 413 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,134-participant average among 91 other Critical Illness trials with a reported enrollment target (87% lower). The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Critical Illness appearing as the primary indexed condition, and to 1 intervention - of which WFIT is the first listed.

NCT04576065 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT04576065 about?

NCT04576065 is a clinical study titled "Wake Forest Post-ICU Telehealth (WFIT) Program". Wake Forest Post-Intensive Care Unit Telehealth (WFIT) program consists of a nurse practitioner who has access to daily activity data as well as telehealth capabilities for 6 months post-hospital discharge in order to improve the post-critical illness care of patients. The study team expects that th...

What is the current status of trial NCT04576065?

This trial is currently completed. It is a NA study. The enrollment target is 413 participants. The study started on 2021-03-19. Estimated completion is 2023-09-14.

What conditions does trial NCT04576065 study?

This clinical trial studies the following conditions: Critical Illness.

What interventions are being tested in trial NCT04576065?

The interventions under investigation include: WFIT (OTHER).

Who is sponsoring clinical trial NCT04576065?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04576065 being conducted?

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

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

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.