FindTrial
Sign In

Evaluation of the effect of immersive virtual reality on improving the labor experience of women undergoing vaginal delivery

Evaluation of the effect of immersive virtual reality on improving the labor experience of women undergoing vaginal delivery: Single-center, randomized controlled clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069689
Enrollment
Unknown
Registered
2023-03-23
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

vaginal delivery

Interventions

Treatment group:Routine care + virtual reality experience
Control group:Routine care

Sponsors

Shenzhen Maternal and Child Healthcare Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.vaginal delivery 2. >=37 weeks of gestation 3. Epidural block labor analgesia has been performed

Exclusion criteria

Exclusion criteria: 1. Severe motion sickness 2. Active nausea and vomiting 3. History of epilepsy 4. Mental illness 5. Visual and audio impairment 6. Prenatal diagnosis of fetal malformations

Design outcomes

Primary

MeasureTime frame
Maternal satisfaction;—

Secondary

MeasureTime frame
pain scores;The change in anxiety scores;Midwife satisfaction;—

Countries

China

Contacts

Public ContactYuantao Li

Shenzhen Maternal and Child Healthcare Hospital

szmchlyt@smu.edu.cn0755-82889999

Outcome results

None listed

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