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Virtual Reality and Its Use in Reducing Perioperative Stress in Cataract Surgery

Virtual Reality and Its Use in Reducing Perioperative Stress in Cataract Surgery

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06822023
Enrollment
75
Registered
2025-02-12
Start date
2025-02-12
Completion date
2025-12-01
Last updated
2025-02-12

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

Conditions

Cataract Surgery, Cataract Surgery Anesthesia, Eye Disease, Virtual Reality

Keywords

cataract surgery, sedation, anxiety, virtual reality

Brief summary

This project is to evaluate the benefits of utilising virtual reality (VR) headsets with the aim of reducing peri-operative anxiety in cataract surgery and hence reducing the need for sedation in patients with significant stress levels noted during preassessment. This is a novel study, and with the increased use of VR technology throughout medicine, we may be able to offer our patients alternative management modalities to reduce stress and reduce need for medications with their subsequent potential side effects. It may also improve the quality of care provided and patients' experience with the cataract extraction procedure and might reduce the social care burden associated with standard sedation procedures. All patients will need to fill a quick preoperative anxiety and information scale questionnaire to assess their level of anxiety utilising The Amsterdam Preoperative Anxiety and Information Score. Patients will be randomised into 2 groups: 1. Conventional group: patients will be prepared as per the standard routine clinical and further explanation of the procedure will be given. Before proceeding to the anaesthetic room, the patients will complete the anxiety score questionnaire again and given the option to proceed with sedation or opt out. 2. Interventional Group: patients will be prepared as per the standard routine clinical care; they will then be wearing the VR mask for 10 minutes. Before proceeding to the anaesthetic room, patients will complete the anxiety score questionnaire again and given the option to proceed with sedation or opt out. Post operation, a record will be taken of the surgeon's decision on whether they want the second eye cataract surgery to be done under sedation (this is already standard practice at our centre). Finally, the patient will be asked to fill in one final grading score on whether they are happy with their decision to take/not take sedation.

Interventions

Patients will be prepared as per the standard routine clinical care; they will then be wearing the VR mask for 10 minutes. No other study have looked into VR mask prior to cataract surgery

Sponsors

South Tyneside and Sunderland NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomised control trial

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Patients listed for cataract surgery under local anaesthetic (topical or regional) with sedation planned. 2. First eye cataract procedures will only be included. 3. Capacity to give informed consent, cognitive and linguistic ability sufficient to understand and fill out questionnaire

Exclusion criteria

1. Epilepsy 2. severe vertigo 3. poor visual acuity (below 6/60 best corrected in the best seeing eye) 4. significant hearing impairment 5. recent facial injury/burn.

Design outcomes

Primary

MeasureTime frameDescription
Anxiety score10 mins following interventionPercentage of reduction in Anxiety score in interventional group as compared to control group as assessed using the Amsterdam preoperative anxiety and information score

Secondary

MeasureTime frameDescription
Patient required sedation after intervention10 minsPercentage of patients who were happy with their decision to undergo/not undergo sedation in intervention vs control group.
Patient required sedation for second eye surgeryFollowing surgery, approximately 30-60 mins following interventionPercentage of patients who the surgeons would list their second eye for sedation in intervention vs control group.

Contacts

Primary ContactJia Y NG, MBChB, FHEA, FRCOphth
jia.ng@nhs.net+441915699954
Backup ContactKaren Davidson
stsft.SEIResearchNurses@nhs.net0191 565 6256

Outcome results

None listed

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