Conversational Artificial Intelligence (AI) to Improve PeRiconception Care Access

NCT06618144 | Completed

• 1 other identifier: OBGYN-PEACE-QI-1
• Study Type: interventional
• Target: 350
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this project, Conversational Artificial Intelligence (AI) to Improve PeRiconception Care Access (CIRCA), is to engage patients in care early in pregnancy (before prenatal care starts) and safely triage concerns to PEACE to reduce unnecessary emergency department visits.

Conditions

Early Pregnancy Loss; Early Pregnancy

Outcome Measures

Primary Outcomes (1)

• Time to initiating care (days)

  Time from first contact to initiating pregnancy related care

  Up to 3 months

Study Arms (1)

CIRCA Texting

EXPERIMENTAL

Participants will be invited to text with a secure, closed artificial intelligence system with clinician oversight to triage patients along predetermined algorithms related to early pregnancy care.

Other: Texting platform

Interventions

Texting platform OTHER

Participants will be invited to text with a secure, closed artificial intelligence system with clinician oversight to triage patients along predetermined algorithms related to early pregnancy care.

CIRCA Texting

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Pregnant
• Seeking to establish care at the Hospital of the University of Pennsylvania OR seeking care in the Emergency Department or Perinatal Evaluation Center.

Sponsors & Collaborators

• University of Pennsylvania: lead
• Memora Health Inc: collaborator
• Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD): collaborator

Study Sites (1)

University of Pennsylvania Health System

Philadelphia, Pennsylvania, 19104, United States

Location

MeSH Terms

Conditions

Abortion, Spontaneous

Condition Hierarchy (Ancestors)

Pregnancy Complications; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 21, 2024
• First Posted: October 1, 2024
• Study Start: August 20, 2024
• Primary Completion: September 21, 2025
• Study Completion: September 21, 2025
• Last Updated: April 2, 2026

Record last verified: 2026-04

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)