About this trial
We want to investigate whether Virtual Reality (VR) could be a good alternative to the relaxing or pain-relieving medications that are often used to alleviate anxiety when patients undergo surgery under local anesthesia.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
over 65 years, planed surgery in local anesthesia/regional anesthesia
Disqualifiers
dementia, unable to cooperate, cognitive impairment
Trial design
Parallel
Treatments tested in this trial
Virtual reality
DeviceParticipant will try virtual reality glasses with tailormade software films to see if it's possible to use them as distraction during awake surgery. We will measure doses of propofol given, level of anxiety, experience of the patient and surgeons satisfaction.
Treatment groups
Trial outcomes
Primary outcomes
propofol mg/kg
dose of propofol given during surgery to the participant
Secondary outcomes
Surgeons satisfaction
surgeons satisfaction, measured with NASA task load index (tlx). Higher score, worse outcome.
Stress/anxiety
Stress or anxiety felt during surgery by participant, measured with State-Trait Anxiety Inventory (STAI) . Higher score worse outcome.
Nurse anesthetists experience, (questionnaire).
Nurse anesthetists experience will be measured with a questionnaire egarding how well the monitoring of the patient could be carried out and the degree to which the patient was perceived as calm. The higher score, the better.
Level of pain
Patients level of pain after surgery, measured with Numeric rating scale (NRS). The higher scores mean worse outcome.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Pether Jildenstal
Lead sponsor
Göteborg University
Sponsor institution
Sahlgrenska University Hospital
Collaborator