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NCT07223736 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by University of California, San Diego.

Not yet
Registry status
NA
Development phase
130
Enrollment target

NCT07223736 is a NA study that has not yet begun recruiting, run by University of California, San Diego. The registered enrollment target is 130 participants.

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The verdict

NCT07223736, a NA study, has not yet begun recruiting, sponsored by University of California, San Diego.

NOT YET RECRUITING
Registry status
NA
Development phase
130 participants
Enrollment target

Study Summary

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.

Interventions

  • OTHER Standard of Care (SOC)
  • OTHER Generative artificial intelligence (genAI) postpartum chatbot

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2025-11-10
Est. Completion 2026-11-01
Phase NA

Sponsor

University of California, San Diego

775 total trials

What the Registry Record Tells You About NCT07223736

The ClinicalTrials.gov registry entry for NCT07223736 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Diego, which has 775 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Standard of Care (SOC) is the first listed.

NCT07223736 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07223736 about?

NCT07223736 is a clinical study titled "Postpartum Education Via Artificial Intelligence for Recovery and Loneliness: A Randomized Controlled Trial". 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 c...

What is the current status of trial NCT07223736?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 130 participants. The study started on 2025-11-10. Estimated completion is 2026-11-01.

What interventions are being tested in trial NCT07223736?

The interventions under investigation include: Standard of Care (SOC) (OTHER), Generative artificial intelligence (genAI) postpartum chatbot (OTHER).

Who is sponsoring clinical trial NCT07223736?

This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.