Risk factors contributing to neurocognitive dysfunction in postpartum women and construction of risk prediction model

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400080632

Enrollment

Unknown

Registered

2024-02-04

Start date

2023-10-10

Completion date

Unknown

Last updated

2024-02-05

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

Conditions

cognitive dysfunction in postpartum women

Interventions

Group A(Those who developed postpartum neurocognitive dysfunction) GroupB(Those who did not develop postpartum neurocognitive dysfunction):none

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: ?Aged = 18 years ?Be able to communicate

Exclusion criteria

Exclusion criteria: ?ASA grade =? ?pregnant women previously diagnosed with an intellectual disability, mental disorder, or epilepsy; ?The Montreal Cognitive Assessment Test score (MoCA) < 26 (Schooling years below 12 years < 27) ?Using hormones or psychotropic drugs ?Refuse or unable to finish prenatal cognitive function tests ?Informed consent was not obtained

Design outcomes

Primary

Measure	Time frame
Incidence of cognitive dysfunction between 6 months after delivery;GiViTi calibrate curve ;	—

Secondary

Measure	Time frame
Scores of five cognitive function tests ;Incidence of depression between 6 months after delivery;Incidence of anxiety between 6 months after delivery;	—

Countries

China

Contacts

Public ContactSu Liu

The Affiliated Hospital of Xuzhou Medical University

150040009@qq.com+86 181 1830 9692

Outcome results

None listed

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