Virtual Reality for Intraoperative Anxiolysis and Postoperative Agitation in Elderely Hip Arthroplasty Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-75
SponsorMenoufia University

About this trial

This study evaluates the effectiveness of Virtual Reality (VR) as a non-pharmacological intervention to reduce intraoperative anxiety and postoperative agitation in elderly patients undergoing elective hip arthroplasty under regional anesthesia. Half of the patients will experience an immersive, calming nature-based VR environment during the surgery, while the control group will receive standard care.

Eligibility criteria

Qualifiers

Patients scheduled for elective cemented or uncemented hip arthroplasty under regional (spinal or epidural) anesthesia.

ASA physical status I-III.

Mentally capable of providing informed consent.

Disqualifiers

Pre-existing cognitive impairment or dementia (as assessed by the Mini-Mental State Examination).

Severe uncorrected visual or hearing impairments that prevent VR device tolerance.

Severe psychiatric disorders (e.g., schizophrenia, bipolar disorder).

General contraindications to regional anesthesia (e.g., localized back infection, severe coagulopathy).

Trial design

Treatments tested in this trial

  • immersive virtual reality
  • standard sedation

Treatment groups

40 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators