Skip to content

Research and Clinical Application of an AI - based Intelligent Assessment and Personalized Intervention System for Perinatal Pain Using Multimodal Signal Fusion Technology

Research and Clinical Application of an AI - based Intelligent Assessment and Personalized Intervention System for Perinatal Pain Using Multimodal Signal Fusion Technology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114508
Enrollment
Unknown
Registered
2025-12-14
Start date
2025-04-07
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Perinatal pain

Interventions

Control group (conventional pain management):None
Research Group (Personalized Pain Intervention):None

Sponsors

The international peace maternity and child health hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Term singleton pregnant women willing to attempt vaginal delivery. 2.No contraindications to vaginal delivery (e.g., fetal abnormalities, fetal distress, pelvic stenosis, scarred uterus, etc.) as assessed by an obstetrician; 3.Full-term pregnant women (gestational age =37 weeks, confirmed by ultrasound examination); 4.Singleton pregnancy; 5.Healthy pregnant volunteers without severe pregnancy complications/comorbidities (e.g., severe preeclampsia, uncontrolled gestational diabetes mellitus, etc.); 6.Informed consent: voluntary participation in the study, provision of written informed consent, and ability to cooperate with study-related procedures such as baseline data collection, delivery process documentation, and follow-up.

Exclusion criteria

Exclusion criteria: 1.Presence of contraindications to vaginal delivery (e.g., fetal abnormalities, fetal distress, pelvic stenosis, scarred uterus, etc.); 2.Underlying diseases and comorbidities: severe cardiovascular diseases (e.g., heart failure, severe arrhythmia), severe hepatic or renal dysfunction, coagulation disorders, active infectious diseases (e.g., AIDS, active syphilis, active tuberculosis), malignancies, etc. 3.Lack of willingness to attempt vaginal delivery, explicit request for elective cesarean section, or voluntary discontinuation of the trial of labor during the process due to non-medical reasons; 4.Special populations such as patients with psychiatric disorders, cognitive impairment, or those unable to communicate effectively (e.g., language barriers without translation support).

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale, VAS, 0-100 mm;Numerical Rating Scale, NRS, 0-10 points;

Countries

China

Contacts

Public ContactXiaona Xu

The international peace maternity and child health hospital

ggappsong@sjtu.edu.cn+86 21 6407 0434

Outcome results

None listed

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