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Recruiting NCT07234201

Virtual Reality Use for ICU Mobility

No phase Interventional Intensive Care Unit ICU

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Nurse driven virtual reality mobility session.
Who it may be relevant to
Registry conditions: Intensive Care Unit ICU. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Designing a Virtual Reality Intervention to Improve Physical and Psychological Health in Intensive Care Units

Overview

The purpose of this study is to explore if Virtual Reality (VR) helps patients in the Intensive Care Unit (ICU) move more and feel better.

Interventions

  • Other Nurse driven virtual reality mobility session
    Participants will use the virtual reality device to play the game that will facilitate movement of arms, shoulders and trunk to music, similar to dancing or Tai-Chi.

Primary outcome measures

  • Number of participants with Increased Mobility [Time frame: 10 days or ICU discharge, which ever comes first]
Secondary outcome measures (1)
  • Number of participants with Improved psychosocial well-being [Time frame: 10 days or ICU discharge, which ever comes first]

Eligibility criteria

Inclusion criteria

  • English speaking
  • Adults age 18 or greater
  • ICU stay greater or equal to 3 days
  • Limited mobility

Exclusion criteria

  • Pregnancy
  • Special enteric contact isolation
  • Blindness
  • History of seizure or vertigo
  • Intubated and sedated
  • ICU delirium

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

United States · 1 center
  • Duke University Hospital — Durham

Identifiers

NCT: NCT07234201 · PRO00116448_1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗