Smart Normal Labor: Healthcare Providers' Experience With an AI-Based Mobile App

ConditionNormal Labor
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorDelta University for Science and Technology

About this trial

Pregnancy and childbirth are uniquely important events in women's lives because they are accompanied by major physical, emotional, and psychological changes. Maternal satisfaction, emotional well-being, and perceptions of childbirth are strongly influenced by the quality of labor management. A woman's childbirth experience is shaped by multiple factors, including communication, autonomy, and active participation in the decision-making process. These factors are widely recognized as important indicators of the quality of maternity care. \[1\]

Recent demographic changes and global population growth have placed increasing demands on healthcare systems, particularly maternal health services. High birth rates in some regions, combined with shortages of trained healthcare professionals, have created a need for scalable, adaptable, and innovative models of care. In response to these challenges, digital health technologies have emerged as promising tools to enhance the quality of maternity care and support both healthcare providers and pregnant women. \[2\]

Eligibility criteria

Qualifiers

Healthcare providers (obstetricians and nurses) currently working in the Labor Kiosk, Obstetrics and Gynecology Department, or Outpatient Gynecology Clinics at Mansoura University Hospital.

Direct involvement in the care and supervision of women in active labor.

For the intervention group: previous exposure to and use of the AI-based smart normal labor application for a minimum defined period (e.g., 1 month).

For the control group: no prior use of the AI-based application, following standard care practices.

Disqualifiers

Are healthcare providers not directly involved in labor management (e.g., administrative staff or laboratory personnel).

Have less than the minimum required clinical experience in labor management (e.g., <6 months).

Are on leave or unavailable during the study period.

Decline to participate or do not provide informed consent.

Trial design

Treatments tested in this trial

  • The intervention group

Treatment groups

427 Participants
are divided into 2 treatment groups