Adapting the Penny Chatbot for Perinatal OUD Patients: COPILOT

Recruiting N/A Interventional Study
Perinatal Opioid Use Disorder Opioid Use Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Sex
Female
Study type
Interventional
Purpose
Supportive Care
Participants needed
20 (estimated)
Sponsor
University of Pennsylvania · Other
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About This Trial
To address both loneliness and engagement in perinatal and OUD care among perinatal women, the investigators plan to adapt an existing texting support chatbot, Penny, to make it appropriate for use by women who are pregnant and postpartum and dealing with OUD. The newly adapted chatbot, Penny COPILOT, will allow for two way short message service (SMS) messaging to respond appropriately and accurat…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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 a…
Contacts

Sara L Kornfield, PhD

1-800-789-7366

sarakorn@pennmedicine.upenn.edu

CONTACT