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Clinical Trials/NL-OMON49167
NL-OMON49167
Recruiting
Not Applicable

The effect of Virtual Reality on post-surgical pain and recovery - VIRTUAL study

Radboud Universitair Medisch Centrum0 sites100 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Radboud Universitair Medisch Centrum
Enrollment
100
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Patient underwent elective surgery.
  • 2\. Patient reports a postoperative pain score \*4 on the first postoperative day
  • at the surgical ward. Pain scores will be derived from EPIC en should also be
  • marked with \*pain is not acceptable\*.
  • 3\. At the day of recruitment, the estimated length of stay is at least 4 days
  • after inclusion.
  • 4\. Patient is willing and able to comply with the trial protocol.
  • 5\. Patient is at least 16 years old on the day the informed consent form will

Exclusion Criteria

  • 1\. Patient suffers from delirium or acute confusional state.
  • 2\. Patient has (a history of) dementia, seizure, or epilepsy.
  • 3\. Patient with severe hearing/visual impairment not corrected.
  • 4\. Patient is placed in isolation.
  • 5\. The skin of the patient\*s head or face is not intact (for example head
  • wounds, psoriasis, eczema).
  • 6\. Unplanned (re)admission to the intensive care unit (ICU).
  • 7\. Inclusion in another trial to evaluate new ways of treating pain

Outcomes

Primary Outcomes

Not specified

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