Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06373341

Hand and Arm Rehabilitation Using VR

Led by Frisius Medisch Centrum · Updated on 2024-04-18

108

Participants Needed

1

Research Sites

154 weeks

Total Duration

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AI-Summary

What this Trial Is About

Patients admitted to the ICU due to critical illness often experience physical, mental, cognitive, or social issues. Research indicates that inadequate physical recovery is associated with lower handgrip strength, and hand function in ICU patients is lower compared to healthy individuals. To address this, a Virtual Reality (VR) exergame was developed to aid rehabilitation. This study aims to investigate the effect of a 4-week VR-exergame intervention on handgrip strength, hand and arm functionality, balance, mobility, and support needs in ICU patients staying for 48 hours or longer. It is a multicenter mixed-methods randomized controlled trial involving adult ICU patients. The intervention involves a 4-week VR-exergame program. Main study parameters include handgrip strength, hand and arm functionality, range of motion, balance, mobility, and support needs. The burden and risks associated with participation are minimal, as VR-based exercises are deemed safe and voluntary. Overall, the study aims to assess the effect of incorporating VR-based rehabilitation into standard care for ICU patients.

CONDITIONS

Official Title

Hand and Arm Rehabilitation Using VR

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Stay in the ICU for 48 hours or longer
  • Lives in the catchment area of one of the Frisian hospitals
  • Understands the Dutch language
  • Has intact motor skills in at least one upper extremity
Not Eligible

You will not qualify if you...

  • Active delirium (CAM-ICU score 1 or higher)
  • Severe cognitive dysfunction
  • Has an internal cardiac defibrillator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dept of intensive care, Medical Centre Leeuwarden

Leeuwarden, Provincie Friesland, Netherlands, 8901 BR

Actively Recruiting

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Research Team

L

Lise Beumeler, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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