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NCT06829979 · ClinicalTrials.gov registry record · NA

Improving Night Shift Nurses' Health and Reducing Burnout

A NA study, sponsored by University of Pittsburgh.

Completed
Registry status
NA
Development phase
5
Enrollment target

NCT06829979: Completed NA study, sponsored by University of Pittsburgh.

NCT06829979 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 5 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06829979, a NA study, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
NA
Development phase
5 participants
Enrollment target

Study Summary

Healthy and happy nurses are essential to ensuring optimal patient outcomes and organizational success. The evidence on the negative impacts of night shift on nurses' health and cognitive function, and their implications on patient outcomes and organizational costs, reflect the need for interventions to mitigate these detrimental outcomes. This pilot, feasibility, clinical trial will examine the feasibility of two fatigue countermeasure interventions (access to napping/relaxation room and use of blue/green light blocking glass during night shift) and explore the interventions effects on nurses' health, missed care, and burnout.

Primary Outcome

Number of potential participants screened in order to enroll 8 participants

Interventions

  • BEHAVIORAL Access to napping/relaxation room
  • OTHER Blue and green light blocking glasses

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2025-05-23
Est. Completion 2025-12-31
Phase NA
University of Pittsburgh

1,238 total trials

What the finished NCT06829979 record still lists

NCT06829979 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 2 interventions - of which Access to napping/relaxation room is the first listed.

NCT06829979 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06829979 about?

NCT06829979 is a clinical study titled "Improving Night Shift Nurses' Health and Reducing Burnout". Healthy and happy nurses are essential to ensuring optimal patient outcomes and organizational success. The evidence on the negative impacts of night shift on nurses' health and cognitive function, and their implications on patient outcomes and organizational costs, reflect the need for intervention...

What is the current status of trial NCT06829979?

This trial is currently completed. It is a NA study. The enrollment target is 5 participants. The study started on 2025-05-23. Estimated completion is 2025-12-31.

What interventions are being tested in trial NCT06829979?

The interventions under investigation include: Access to napping/relaxation room (BEHAVIORAL), Blue and green light blocking glasses (OTHER).

Who is sponsoring clinical trial NCT06829979?

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

How this trial's enrollment target compares

Where NCT06829979's enrollment target sits among peer trials

5 1988th of 2000 higher than 5 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

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Source: ClinicalTrials.gov NCT06829979, the US trial registry maintained by the National Library of Medicine. NCT06829979 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.