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The influence of virtual reality (VR) multi - stage intervention on preoperative anxiety and rehabilitation of adult patients undergoing elective surgery

The influence of virtual reality (VR) multi - stage intervention on preoperative anxiety and rehabilitation of adult patients undergoing elective surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105910
Enrollment
Unknown
Registered
2025-07-14
Start date
2025-07-15
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Anxiety or fear-related disorder, not specified

Interventions

Control Group:None
Immersive Surgery Room Tour Group:Preoperative visit with VR video
Immersive Surgery Room Tour + Immersive Music Intervention Group:Preoperative visit in the VR video ward combined with immersive music intervention (self-selected music) during the waiting period for

Sponsors

Department of Anesthesia and perioperative Medicine,THE SECOND HOSPITAL OF ANHUI MEDICAL UNIVERSITY
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 45 years old. 2. Plans to undergo the first elective surgery under general anesthesia within the next one week. 3. Those who, after fully explaining the clinical trial content, voluntarily join and sign the informed consent form. 4. Users of Mandarin. 5. Classified as I or II level according to the Physical Status Classification System of the American Society of Anesthesiologists (ASA).

Exclusion criteria

Exclusion criteria: 1. Those who require emergency surgery but have not undergone preoperative assessment, 2. Those with cognitive impairment or inability to consent, 3. Those with any history of psychological disorders, 4. Those with vestibular dysfunction, motion sickness history or visual and auditory dysfunction, 5. Those suffering from Parkinson's disease, multiple sclerosis or muscular dystrophy.

Design outcomes

Primary

MeasureTime frame
Amsterdam Preoperative Anxiety and Information Scale;

Secondary

MeasureTime frame
Athens Insomnia Scale;Simulation Sickness Questionnaire;Stress Level;Pain Level;

Countries

China

Contacts

Public ContactHu Xianwen

Department of Anesthesia and perioperative Medicine,THE SECOND HOSPITAL OF ANHUI MEDICAL UNIVERSITY

huxianwen001@163.com+86 177 6443 3509

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026