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NCT06876168 · ClinicalTrials.gov registry record

Virtual Reality in ICU - PARTNER

A clinical trial of Sepsis and Acute Respiratory Failure, sponsored by Kirby Mayer.

Recruiting
Registry status
32
Enrollment target
1
Study location

NCT06876168: Recruiting study of Sepsis and Acute Respiratory Failure, sponsored by Kirby Mayer.

NCT06876168 is a study of Sepsis and Acute Respiratory Failure that is actively recruiting participants, run by Kirby Mayer. The registered enrollment target is 32 participants, below the 6,564-participant average among 90 other Sepsis trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06876168, a study of Sepsis and Acute Respiratory Failure, is actively recruiting participants, sponsored by Kirby Mayer.

RECRUITING
Registry status
32 participants
Enrollment target
1
Study location

Study Summary

This project is designed to have patients participate in a virtual environment with various tasks such as breathing exercises, games to help the brain, and techniques that promote relaxation while hospitalized in the Intensive Care Unit (ICU). The participation in research will last about 5 days and take about 15 to 45 minutes each day.

Primary Outcome

System Usability Scale - describing the ease of use of the procedure and device

Study Locations (1)

Kentucky

  • University of Kentucky - Lexington

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2025-07-02
Est. Completion 2026-09-30
Kirby Mayer

4 total trials

What NCT06876168 shows while recruiting

NCT06876168 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 6,564-participant average among 90 other Sepsis trials with a reported enrollment target (100% lower).

The record links to 2 conditions, with Sepsis appearing as the primary indexed condition, and to 0 interventions.

NCT06876168 reports a single indexed study location in Kentucky.

Frequently Asked Questions

What is clinical trial NCT06876168 about?

NCT06876168 is a clinical study titled "Virtual Reality in ICU - PARTNER". This project is designed to have patients participate in a virtual environment with various tasks such as breathing exercises, games to help the brain, and techniques that promote relaxation while hospitalized in the Intensive Care Unit (ICU). The participation in research will last about 5 days and...

What is the current status of trial NCT06876168?

This trial is currently recruiting. The enrollment target is 32 participants. The study started on 2025-07-02. Estimated completion is 2026-09-30.

What conditions does trial NCT06876168 study?

This clinical trial studies the following conditions: Sepsis, Acute Respiratory Failure.

Who is sponsoring clinical trial NCT06876168?

This trial is sponsored by Kirby Mayer, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06876168 being conducted?

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

Similar trials for Sepsis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06876168's enrollment target sits among peer trials

32 80th of 90 higher than 11 of 90 other Sepsis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Sepsis 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

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Source: ClinicalTrials.gov NCT06876168, the US trial registry maintained by the National Library of Medicine. NCT06876168 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.