No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Supportive Care
Participants needed
130 (estimated)
Sponsor
University of California, San Diego · Other
Who this trial is looking for
This trial is looking for new mothers who want help with pelvic floor health and feelings of loneliness after childbirth. Participants will receive either standard care or standard care plus access to a supportive chatbot for four weeks.
Are You a Good Fit for This Trial?
Rules you outMajor neonatal anomalyPsychiatric history requiring hospitalizationOther psychiatric conditions needing immediate attention
You may be able to join if
I can provide informed consent
I am willing to follow the study procedures
I am a new mother and at least 18 years old
I have given birth for the first time
I had either a vaginal or cesarean delivery
I speak English
I have internet access and can use it
I have a smartphone
You may not be able to join if
I have given birth before
My baby has a major health issue
I delivered before 34 weeks of pregnancy
I had a stillbirth
I am involved in other conflicting studies
My baby had to go to the NICU
I went home without my baby
I am currently pregnant
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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 feelin…
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Has the capacity to provide informed consent
2. Stated willingness to comply with all study procedures and availability for the duration of the study
3. Postpartum persons, aged \>18 years old
4. Primiparous
5. Vaginal or cesarean delivery
6. English Speaking
7. Internet acce…
Inclusion Criteria:
1. Has the capacity to provide informed consent
2. Stated willingness to comply with all study procedures and availability for the duration of the study
3. Postpartum persons, aged \>18 years old
4. Primiparous
5. Vaginal or cesarean delivery
6. English Speaking
7. Internet access and proficiency of internet access
8. Access to a smartphone
9. Postpartum 2-6 weeks
Exclusion Criteria:
1. Multiparous
2. Major neonatal anomaly
3. Delivery \< 34 weeks gestational age
4. Intrauterine fetal demise (IUFD)
5. Enrollment in any interfering studies
6. Unanticipated NICU admission
7. Discharge home without live baby
8. Surrogates/gestational carrier
9. Birthing individuals with baby placed for adoption
10. Currently pregnant
11. Psychiatric history requiring psychiatric hospitalization prior to delivery
12. Other psychiatric conditions needing immediate attention and intervention as determined by study team and/or treatment team
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