Actively Recruiting
Adapting the Penny Chatbot for Perinatal Opioid Use Disorder Patients: COPILOT
Led by University of Pennsylvania · Updated on 2026-02-13
20
Participants Needed
2
Research Sites
4 weeks
Total Duration
On this page
Sponsors
U
University of Pennsylvania
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The opioid epidemic in the US affects women of childbearing age, with a significant increase in opioid use disorder (OUD) among women giving birth. This research aims to adapt a texting support chatbot, Penny, to better support pregnant and postpartum women dealing with OUD. The adapted chatbot, Penny COPILOT, is designed to reduce loneliness, improve engagement in perinatal and OUD care, and address challenges like limited access to in-person visits and social isolation during the perinatal period. The study uses a single-arm design to assess the acceptability and feasibility of Penny COPILOT, which is an interactive SMS program providing educational and support messages tailored for postpartum individuals with OUD. The chatbot enables two-way messaging and sends content relevant to OUD recovery at specific postpartum intervals. The study includes three main phases: a needs assessment with interviews, pretesting with 10 patients to refine the chatbot and ensure safety, and a pilot test with 20 patients to evaluate user satisfaction and feasibility. Participants will engage with the chatbot and complete assessments during the pilot phase, including surveys and electronic medical record reviews to measure loneliness, social isolation, opioid use, mental health, and healthcare engagement. The primary outcome is measured using the UCLA Loneliness Scale at baseline and 3 months follow-up. The study also collects data on opioid use through questionnaires. The total study duration includes these phases and follow-up assessments to evaluate the chatbot’s impact and user experience.
CONDITIONS
Brief Title
Adapting the Penny Chatbot for Perinatal OUD Patients: COPILOT
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Biological females who are currently pregnant or within 6 weeks postpartum.
- Able to read, write, and speak English at a 6th grade level.
- Diagnosed and receiving treatment for, or willing to receive treatment for opioid use disorder.
- Receiving prenatal care and OUD care at a Penn affiliated hospital.
You will not qualify if you...
- Current untreated psychosis, mania, or active suicidality as assessed by the Mini International Neuropsychiatric Interview (MINI).
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 3 months
Participants use the Penny COPILOT chatbot, an interactive SMS program providing educational and supportive content relevant to opioid use disorder recovery during the postpartum period.
Regular interactions via SMS throughout the treatment period
Duration - 3 months
Participants complete self-report surveys and assessments at baseline and 3 months to evaluate loneliness, opioid use, mental health, and healthcare engagement.
2 visits (baseline and 3-month follow-up)
Trial Site Locations
Total: 2 locations
1
Hospital of the University of Pennsylvania (HUP)
Philadelphia, Pennsylvania, United States, 19072
Actively Recruiting
2
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104-3309
Not Yet Recruiting
Research Team
S
Sara L Kornfield, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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