NCT07270445 Effect of Virtual Reality Use on Preoperative Anxiety
| NCT ID | NCT07270445 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Vera Guttenthaler |
| Condition | Anxiety |
| Study Type | INTERVENTIONAL |
| Enrollment | 172 participants |
| Start Date | 2026-01-28 |
| Primary Completion | 2026-12-14 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 172 participants in total. It began in 2026-01-28 with a primary completion date of 2026-12-14.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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 Criteria
Inclusion Criteria: * 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 Exclusion Criteria: * Patients undergoing emergency surgery * Patients with documented psychiatric disorders (e.g., bipolar disorder), confusion, or epilepsy * Individuals admitted due to a court or official order * Expected non-compliance with the study protocol * Expected admission to an intermediate care unit (IMC) or intensive care unit (ICU) * Patients receiving sedative or anxiolytic medication for premedication * Patients with pacemakers or defibrillators
Frequently Asked Questions
Who can join the NCT07270445 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Anxiety. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07270445 currently recruiting?
Yes, NCT07270445 is actively recruiting participants. Visit ClinicalTrials.gov or contact Vera Guttenthaler to inquire about joining.
Where is the NCT07270445 trial being conducted?
This trial is being conducted at Bonn, Germany.
Who is sponsoring the NCT07270445 clinical trial?
NCT07270445 is sponsored by Vera Guttenthaler. The trial plans to enroll 172 participants.
Related Trials
Related Intelligence Guides
In-depth guides covering this condition's trials, eligibility, and what to expect.