Virtual Reality as a Digital Premed to Alleviate Pain and Anxiety Preoperatively in Patients Undergoing Spine Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age25-70
SponsorMedical University of Lodz

About this trial

The aim of this research study is to evaluate the impact of immersive VR exposure on preoperative anxiety and pain. Additionally, to assess whether VR intervention would significantly alleviate pain and anxiety levels of patients undergoing complex spinal surgeries. Investigators hypothesize that the application of pre-operative VR-based intervention will alleviate anxiety and pain both pre- and post-operatively when it is used as treatment to complement standard care compared to standard routine care alone, and that it may lead to better outcomes and higher satisfaction in patients.

Eligibility criteria

Qualifiers

Adult patients between 25-70 years old, undergoing an elective spinal surgery.

Patient's admission prior to surgery day (at least 1 day).

Expected hospital stay - 2 days.

Capable of providing informed consent and participate in the study follow-up questionnaire.

Disqualifiers

Congestive heart failure, hypertension and anti-hypertensive medications

Adrenal insufficiency

Alcohol addiction (evaluated by CAGE/AUDIT) and substance addiction (evaluated by DUDIT)

Cognitive impairment (evaluated by MMSE, MoCA)

Trial design

Treatments tested in this trial

  • Virtual Reality

Treatment groups

150 Participants
are divided into 3 treatment groups

Sponsors and collaborators