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NCT06014931 · ClinicalTrials.gov registry record · NA

Telehealth-enhanced Patient-oriented Recovery Trajectory After Intensive Care

A NA study of Post-Intensive Care Syndrome, sponsored by Vanderbilt University.

Recruiting
Registry status
NA
Development phase
202
Enrollment target
2
Study locations

NCT06014931 is a NA study of Post-Intensive Care Syndrome that is actively recruiting participants, run by Vanderbilt University. The registered enrollment target is 202 participants, above the 154-participant average among 5 other Post-Intensive Care Syndrome trials with a reported enrollment target (31% higher). The trial reports 2 study locations across 2 states.

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The verdict

NCT06014931, a NA study of Post-Intensive Care Syndrome, is actively recruiting participants, sponsored by Vanderbilt University.

RECRUITING
Registry status
NA
Development phase
202 participants
Enrollment target
2
Study locations

Study Summary

Intact cognitive skills are necessary for independent living, going to work, and managing finances, and any loss of cognitive skills places a burden on society akin to what is seen with Alzheimer's Disease and Related Dementias. The TelePORT Study (Telehealth-Enhanced Patient-Oriented Recovery Trajectories after Intensive Care) is the first post-intensive care syndrome longitudinal long-term cognitive impairment intervention study. The societal effect from long-term cognitive impairment after critical illness is great as many of these patients are employable adults or functional retirees.

Conditions Studied

Post-Intensive Care Syndrome

Interventions

  • BEHAVIORAL Telemedicine ICU Recovery Clinic Visit

Study Locations (2)

Ohio

  • Ohio State University Wexner Medical Center - Columbus

Tennessee

  • Vanderbilt University Medical Center - Nashville

Trial Details

FieldValue
Enrollment Target 202 participants
Start Date 2024-03-13
Est. Completion 2028-05-31
Phase NA

Sponsor

Vanderbilt University

430 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06014931

The ClinicalTrials.gov registry entry for NCT06014931 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 202 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 154-participant average among 5 other Post-Intensive Care Syndrome trials with a reported enrollment target (31% higher). The listed sponsor is Vanderbilt University, which has 430 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Post-Intensive Care Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Telemedicine ICU Recovery Clinic Visit is the first listed.

NCT06014931 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Ohio, Tennessee.

Frequently Asked Questions

What is clinical trial NCT06014931 about?

NCT06014931 is a clinical study titled "Telehealth-enhanced Patient-oriented Recovery Trajectory After Intensive Care". Intact cognitive skills are necessary for independent living, going to work, and managing finances, and any loss of cognitive skills places a burden on society akin to what is seen with Alzheimer's Disease and Related Dementias. The TelePORT Study (Telehealth-Enhanced Patient-Oriented Recovery Traje...

What is the current status of trial NCT06014931?

This trial is currently recruiting. It is a NA study. The enrollment target is 202 participants. The study started on 2024-03-13. Estimated completion is 2028-05-31.

What conditions does trial NCT06014931 study?

This clinical trial studies the following conditions: Post-Intensive Care Syndrome.

What interventions are being tested in trial NCT06014931?

The interventions under investigation include: Telemedicine ICU Recovery Clinic Visit (BEHAVIORAL).

Who is sponsoring clinical trial NCT06014931?

This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06014931 being conducted?

This trial has 2 study locations across Ohio, Tennessee. 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.