Knowledge of pelvic floor disorder in pregnancy.
Jiayi Liu, Shu Qi Tan, How Chuan Han
https://pubmed.ncbi.nlm.nih.gov/30783706/Actively Recruiting
Led by University of California, San Diego · Updated on 2026-08-05
130
Participants Needed
1
Research Sites
4 weeks
Total Duration
Researchers are evaluating a postpartum chatbot powered by generative artificial intelligence genAI to see if it can improve pelvic floor health knowledge and reduce feelings of loneliness in new mothers after childbirth. This trial focuses on postpartum individuals who have recently given birth and aims to compare standard postpartum care with and without the addition of this chatbot. The study addresses the common challenges postpartum individuals face, including pelvic floor disorders, mental health issues, and social isolation, which can affect both maternal and infant well-being. Participants will be randomly assigned to either receive standard postpartum care or standard care plus access to the genAI chatbot. The chatbot is accessible through a secure web application for 4 weeks following enrollment and provides personalized, evidence-based education and support about pelvic floor health. It operates without requiring extra in-person visits, and usage data will be collected to understand engagement. Both groups will complete questionnaires about pelvic floor knowledge, symptoms, loneliness, depression, infant bonding, social support, and stress-related experiences. During the study, participants will complete assessments at enrollment, after the intervention period or standard care, and again at 6 months postpartum. These include measures of pelvic floor knowledge, distress symptoms, and loneliness scores. The researchers will monitor responses to evaluate the impact of the chatbot on physical and emotional recovery. The total participation includes the initial 4-week chatbot access period plus follow-up assessments extending to 6 months postpartum, providing insight into both short- and longer-term effects.
CONDITIONS
Postpartum Education Via Artificial Intelligence for Recovery and Loneliness: A Randomized Controlled Trial
A
Alexandra C Nutaitis, DO
C
Cecile Ferrando, MD, MPH
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University of California, San Diego
Lead Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | Generative AI-Powered Postpartum Chatbot Education | Standard Postpartum Care |
|---|---|---|
| What is it? | Participants access a secure AI chatbot on their smartphones or computers, which provides tailored postpartum pelvic floor education and support, available anytime during a four-week window after giving birth. | Participants receive usual postpartum care as provided in their healthcare setting, including routine assessments, information, and support consistent with best practice guidelines. |
| Role in the trial | Investigational arm; assesses engagement, pelvic floor knowledge, distress, and loneliness improvements relative to standard care. | Control arm; provides a benchmark for routine postpartum outcomes and educational experience in comparison to the digital intervention. |
| Primary use | Online education and support for pelvic floor health and loneliness delivered in early postpartum via a conversational AI interface. | Traditional education, support, and clinical follow-up as recommended postpartum practice. |
| How is it given or performed? | Participants use a secure web-based platform on their smartphone or computer for four weeks with unlimited access to the AI chatbot. | Participants attend postpartum visits and consultations as scheduled, receive educational materials and clinician guidance based on standard practice. |
| Evidence status | This specific AI chatbot is under active clinical evaluation; earlier mental health chatbots for postpartum support have shown feasibility and beneficial effects but large-scale evidence remains limited. | Standard postpartum care is supported by established clinical guidelines and routine practice, with robust evidence for patient safety and effectiveness in pelvic floor education, maternal mental health, and support. |
| Important limitations | Engagement depends on participant motivation and digital proficiency, and effectiveness for loneliness and pelvic floor education is not yet established in large-scale controlled studies. | Traditional postpartum care may suffer from inconsistent access, variable educational quality, and limited personalization, with some unmet support needs identified in guidelines and literature. |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 4 weeks
Participants receive either standard postpartum care alone or standard care plus access to the AI-powered chatbot providing pelvic floor education and support for 4 weeks.
Access chatbot anytime during the 4 weeks; complete questionnaires at set times
Duration - Up to 6 months postpartum
Participants complete questionnaires to assess pelvic floor knowledge, symptoms, and feelings of loneliness at enrollment, post-intervention or standard care, and at 6 months postpartum.
3 questionnaire time points: enrollment, post-intervention, 6 months postpartum
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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https://pubmed.ncbi.nlm.nih.gov/38217763/University of California, San Diego
Lead Sponsor