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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: Clinical Trial NA study, sponsored by University of California, San Diego.

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, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

Prolapse and incontinence knowledge will be assessed via the validated prolapse and incontinence knowledge questionnaire (PIKQ). This is a validated, self-administered instrument designed to assess women's knowledge about the epidemiology, pathogenesis, diagnosis, and treatment of pelvic organ prolapse and urinary incontinence. The PIKQ has been used in the postpartum population.This questionnaire consists of two 12 item sub-scales (total of 24 questions) with answer options of "agree", "disagre

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
University of California, San Diego

775 total trials

What is known before NCT07223736 opens enrollment

NCT07223736 is an interventional study that assigns participants to a tested intervention. The registered 130 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower).

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

NCT07223736 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT07223736's enrollment target sits among peer trials

130 733rd of 2000 higher than 1,257 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07223736, the US trial registry maintained by the National Library of Medicine. NCT07223736 (mid enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.