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Effect of Virtual Reality Use on Preoperative Anxiety: A Prospective, Randomized, Controlled Interventional Study (VeRA-Study)

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of this study is to investigate the effect of a non-pharmacological intervention-the use of a virtual reality headset-on preoperative anxiety levels in patients. For this purpose, both psychometric instruments (STOA and APAIS questionnaires) and objective physiological and EEG parameters are used. Patients who do not receive any additional intervention will form the control group. The study was designed as a prospective, randomized, controlled, interventional study at the University Hospital Bonn. Patients aged 18 years and older who are scheduled to undergo elective surgery and who have no visual, hearing, or language impairments will be included in the study. The primary objective of the study is the reduction of preoperative anxiety. The hypothesis is that preoperative use of the VR headset reduces perioperative anxiety, stress, and pain.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years

• Written informed consent

• All consecutive patients undergoing elective, outpatient, or inpatient surgery

• No communication difficulties (e.g., hearing impairment) and good command of the German language

• No visual impairment

• Planned extubation immediately after surgery

Locations
Other Locations
Germany
University of Bonn
RECRUITING
Bonn
Time Frame
Start Date: 2026-01-28
Estimated Completion Date: 2027-03-01
Participants
Target number of participants: 172
Treatments
Experimental: Virtual reality glasses
No_intervention: Control
Related Therapeutic Areas
Sponsors
Leads: Vera Guttenthaler

This content was sourced from clinicaltrials.gov