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A randomized controlled trial to determine whether a video presentation improves informed consent for Cesarean section

A randomized controlled trial to determine whether a video presentation improves informed consent for Cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021463
Enrollment
Unknown
Registered
2019-02-22
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

preoperation informed consent

Interventions

Group 1:video presentation
Group 2:traditional preoperation informed consent

Sponsors

Guangzhou Women and Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Pregnancy women who will elective caesarean section; 2. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Additional surgery in caesarean section; 2. Participate in other studies.

Design outcomes

Primary

MeasureTime frame
Knowledge Understanding Ability of Cesarean Section;—

Countries

China

Contacts

Public ContactJinying Yang

Guangzhou Women and Children's Medical Center

yangjinying1981@126.com+86 13560092369

Outcome results

None listed

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