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Anxiolytic Effectiveness of Virtual Reality Glasses in Surgery

Anxiolytic Effectiveness of Virtual Reality Glasses in Upper Extremity Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06244654
Enrollment
86
Registered
2024-02-06
Start date
2024-01-25
Completion date
2024-07-15
Last updated
2025-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Anxiety, Postoperative Pain, Postoperative Recovery

Brief summary

Regional anesthesia allows surgery without affecting the patient's level of consciousness.However, this may cause anxiety in some patients.In previous research, scientists have tried to prevent anxiety with non-pharmacological interventions such as music and cognitive therapies.Virtual reality is thought to offer an immersive experience that can alter the mind's perception of pain. Scientists have found in previous preliminary studies that virtual reality is safe and effective as an adjunct to standard sedative/analgesic protocols for reducing patients' pain and anxiety during endoscopy, colonoscopy, dental treatments, burn dressings, and labor. In this study, it is expected that anxiety scores, postoperative analgesic need and intraoperative sedation need will decrease, recovery quality will improve and patient satisfaction will increase in patients who will undergo upper extremity surgery under regional anesthesia and watch videos through VR glasses.

Interventions

DEVICEOculus Quest 2 VR virtual reality glasses and wired over-ear headphones

After the VR group comes to the preoperative area and is evaluated, they will be asked to wear VR glasses and headphones. VR glasses and headphones were worn on the patient during peripheral nerve block applications and the operation. At the end of the operation, the VR glasses and headphones were removed and they were taken to the postoperative recovery room.

OTHERNo VR

After evaluation of the patients taken to the preoperative area, routine peripheral nerve block application was performed without the use of VR glasses. VR glasses were not worn during the operation, as is the routine protocol. At the end of the surgery, they were taken to the postoperative recovery room.

Sponsors

Ankara City Hospital Bilkent
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* who will undergo upper extremity surgery under regional anesthesia

Exclusion criteria

* being under 18 years old * Those who do not have the ability to read, understand and sign the consent form * An active infection or open wound in the face or eye area * History of seizures due to an epileptic condition or any other reason * Planning to wear a hearing aid during the surgical procedure * Having a pacemaker or other implanted medical device * Migraine * Having an infectious condition that is transmitted through droplets or airborne * not knowing Turkish * Not deemed suitable for the approach by the surgeon * History of psychosis or claustrophobia * Being visually and/or hearing impaired

Design outcomes

Primary

MeasureTime frameDescription
State-Trait Anxiety ScalePreoperative, Postoperative 4.hourpreoperative and postoperative STAI I and II score questions will be asked.

Secondary

MeasureTime frameDescription
diastolic blood pressurePreoperative, İntraoperative 0 min, İntraoperative 60min, End of Operation, Postoperative 4.hournon invasive diastolic blood pressure measurement
mean arterial pressurePreoperative, İntraoperative 0 min, İntraoperative 60min, End of Operation, Postoperative 4.hourmean blood pressure measurement
heart ratePreoperative, İntraoperative 0 min, İntraoperative 60min, End of Operation, Postoperative 4.hourintraoperatif and perioperatif ecg monitarization
oxygen saturationPreoperative, İntraoperative 0 min, İntraoperative 60min, End of Operation, Postoperative 4.hourintraoperatif and perioperative pulse oxymeter measurement
systolic blood pressurePreoperative, İntraoperative 0 min, İntraoperative 60min, End of Operation, Postoperative 4.hournon invasive systolic blood pressure measurement
VAS scorePostoperative 1.hour, 4.hour., 12.hour., 24hour.A blinded evaluator will evaluate the visual analog scale score.
Patient satisfaction scalePostoperative 4.hourA blinded evaluator will evaluate the Patient satisfaction scale
Surgeon satisfaction scalePostoperativ 1.hourA blinded evaluator will evaluate the surgeon satisfaction scale
The quality of recovery-15 (QoR-15)Preoperative, Postoperative 24.hourA blinded evaluator will evaluate the QoR-15 scale.
aditional analgesic requirementpostoperative up to 24 hourpostoperative additional analgesic requirement

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026