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Efficacy of virtual reality intervention for preventing postpartum depression during cesarean section: a multicenter, randomized controlled trial

Efficacy of virtual reality intervention for preventing postpartum depression during cesarean section: a multicenter, randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113978
Enrollment
Unknown
Registered
2025-12-04
Start date
2025-12-10
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Postpartum depression

Interventions

Virtual reality group:Virtual reality video and routine care.
Routine care group:Routine care

Sponsors

Shenzhen Maternity & Child Healthcare Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Elective cesarean section; 2.The proposed method of anesthesia is neuraxial anesthesia.

Exclusion criteria

Exclusion criteria: 1.History of vestibular dysfunction or motion sickness; 2.History of epilepsy; 3.Audiovisual impairment; 4.American Society of Anesthesiologists physical status III or higher.

Design outcomes

Primary

MeasureTime frame
The prevalence of postpartum depression at 42 days post partum;—

Secondary

MeasureTime frame
The proportion of breastfeeding at 42 days post partum;The proportion of breastfeeding at 7 days post partum;Intraoperative satisfaction score;Edinburgh postnatal depression scale score at 7 days post partum;Edinburgh postnatal depression scale score at 42 days post partum;Intraoperative anxiety score;—

Countries

China

Contacts

Public ContactYuantao Li

Shenzhen Maternity & Child Healthcare Hospital

sylyt6788@sina.com+86 755 8288 9999

Outcome results

None listed

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