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Virtual reality simulation of operating room visits to reduce preoperative anxiety in first-time gynecological Patients: A randomised, single-centre clinical trial

Virtual reality simulation of operating room visits to alleviate preoperative anxiety in gynecological patients: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086858
Enrollment
Unknown
Registered
2024-07-12
Start date
2023-11-20
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

Preoperative anxiety

Interventions

Standard preoperative visit group:Conduct standard preoperative visits
Virtual reality group:Watch VR videos

Sponsors

Lianyungang First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Selection criteria: 1) Age>18 years old; 2) ASA Level I, II, or III 3) Women who have no visual or intellectual disabilities and have undergone gynecological surgery. 4) Willing to cooperate with this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1) Suffering from severe motion sickness and severe neurological disorders. 2) Malignant tumors, patients undergoing emergency surgery 3) Patients with arrhythmia and severe cardiovascular disease. 4) Obstructive sleep apnea, gynecological and obstetric patients with tumors. 5) Women who cannot understand the questionnaire. 6) Patients who have previously entered the operating room for surgery

Design outcomes

Primary

MeasureTime frame
State-Trait Anxiety Inventory (STAI);

Secondary

MeasureTime frame
State-Trait Anxiety Inventory (STAI);Heart rate variability (HRV);Heart rate (HR);Blood pressure (BP);Sleep time;Athens InsomniaScale (AIS);

Countries

China

Contacts

Public ContactZhao Zhibin

Lianyungang First People's Hospital

lygzhaozhibin@163.com+86 189 6132 6661

Outcome results

None listed

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