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The effectiveness of immersive virtual reality in relieving anxiety and improving patient satisfaction during cesarean delivery

The effectiveness of immersive virtual reality in relieving anxiety and improving patient satisfaction during cesarean delivery: a randomized clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061936
Enrollment
Unknown
Registered
2022-07-11
Start date
2022-07-15
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Cesarean delivery

Interventions

Experimental group:virtual reality experience
Control group:None

Sponsors

Shenzhen Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. American Society of Anesthesiologists physical status II; 2. Elective cesarean delivery; 3. Spinal anesthesia.

Exclusion criteria

Exclusion criteria: 1. The fetus is severely deformed; 2. Gestational age < 28 weeks; 3. Severe motion sickness; 4. Mental illness; 5. History of epilepsy; 6. Audiovisual impairment.

Design outcomes

Primary

MeasureTime frame
The change in anxiety scores;—

Secondary

MeasureTime frame
Patient satisfaction;Respiratory rate;Use of sedative and analgesic drugs during operation;—

Countries

China

Contacts

Public ContactLi Yuantao

Shenzhen Maternal and Child Health Hospital

szmchlyt@smu.edu.cn+86 755 82889999

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026