Postpartum Education Via Artificial Intelligence for Recovery and Loneliness: A Randomized Controlled Trial

Recruiting now · Not applicable

Conditions studied: Pelvic Floor Disorder, Loneliness, Postpartum, Mental Health, Depression, Peritraumatic Distress, Women, Artificial Intelligence (AI), Chatbot

In brief

The goal of this clinical trial is to learn whether a postpartum chatbot powered by generative artificial intelligence (genAI) can help new mothers get better pelvic floor health information and feel less lonely after childbirth. The main questions this study aims to answer are: * Does using the chatbot improve postpartum pelvic floor health knowledge? * Does using the chatbot help reduce feelings of loneliness during the postpartum period? * Does using the chatbot impact pelvic floor symptoms? Researchers will compare standard postpartum care to standard care plus the chatbot. Participants will: Be assigned by chance (like flipping a coin) to standard postpartum care with or without access to the chatbot. If in the chatbot group, participants will receive education and support via the chatbot over a 4-week period. Both groups will complete questionnaires to measure their pelvic floor knowledge, pelvic floor symptoms, feelings of loneliness, depression, infant bonding, perceived social support, adverse childhood experiences, and peri-traumatic distress. The chatbot was created by urogynecology experts in collaboration with UC San Diego computer science and biomedical informatics researchers. The chatbot is designed to give new mothers personalized, evidence-based information and support in real time.

Key facts

Study ID

NCT07223736

Run by

University of California, San Diego

People needed

130

Starts

2026-01-08

Expected to finish

2026-11-01

Last updated by the study team

2026-08-05

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Has the capacity to provide informed consent
• Stated willingness to comply with all study procedures and availability for the duration of the study
• Postpartum persons, aged >18 years old
• Primiparous
• Vaginal or cesarean delivery
• English Speaking
• Internet access and proficiency of internet access
• Access to a smartphone
• Postpartum 2-6 weeks

You may not qualify if…

• Multiparous
• Major neonatal anomaly
• Delivery < 34 weeks gestational age
• Intrauterine fetal demise (IUFD)
• Enrollment in any interfering studies
• Unanticipated NICU admission
• Discharge home without live baby
• Surrogates/gestational carrier
• Birthing individuals with baby placed for adoption
• Currently pregnant
• Psychiatric history requiring psychiatric hospitalization prior to delivery
• Other psychiatric conditions needing immediate attention and intervention as determined by study team and/or treatment team

Where it is running

• University of California San Diego — La Jolla, California, United States (enrolling)

Full record on ClinicalTrials.gov

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