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NCT06969261 · ClinicalTrials.gov registry record · NA

Adapting the Penny Chatbot for Perinatal OUD Patients: COPILOT

A NA study of Opioid Use Disorder and Perinatal Opioid Use Disorder, sponsored by University of Pennsylvania.

Recruiting
Registry status
NA
Development phase
20
Enrollment target
2
Study locations

NCT06969261: Recruiting NA study of Opioid Use Disorder and Perinatal Opioid Use Disorder, sponsored by University of Pennsylvania.

NCT06969261 is a NA study of Opioid Use Disorder and Perinatal Opioid Use Disorder that is actively recruiting participants, run by University of Pennsylvania. The registered enrollment target is 20 participants, below the 4,656-participant average among 257 other Opioid Use Disorder trials with a reported enrollment target (100% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06969261, a NA study of Opioid Use Disorder and Perinatal Opioid Use Disorder, is actively recruiting participants, sponsored by University of Pennsylvania.

RECRUITING
Registry status
NA
Development phase
20 participants
Enrollment target
2
Study locations

Study Summary

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 accurately to user generated input. The investigative team, in collaboration with the Penn Mixed Methods Research Lab (MMRL) and Penn's Way 2 Health Team, will use intervention mapping guided by the Consolidated Framework for Implementation Science. The investigators will conduct a needs assessment, assemble an advisory board, engage in pretesting to ensure safety and refine content, and pilot test the resultant adapted Penny COPILOT in a sample of 20 perinatal women with OUD to evaluate acceptability, feasibility, and patient satisfaction. The goal is to develop and refine an acceptable, feasible, and satisfactory supportive texting chatbot to promote patient engagement in perinatal and OUD care and decrease perceived loneliness.

Primary Outcome

The UCLA Loneliness Scale (Version 3) is the most commonly used measure of loneliness, with strong test-retest reliability, high internal consistency, and validity.97 While the word "lonely" is never used explicitly in the 20-item scale, subjects are asked to report the frequency of specific experiences (e.g., "How often do you feel in tune with others around you?") on a 4-point Likert scale (1 = "I never feel this way" to 4 = "I often feel this way.") For dichotomous analysis of loneliness, we

Interventions

  • BEHAVIORAL Penny COPILOT

Study Locations (2)

Pennsylvania

  • Hospital of the University of Pennsylvania (HUP) - Philadelphia
  • University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2026-01-01
Est. Completion 2026-06-30
Phase NA
University of Pennsylvania

1,423 total trials

What NCT06969261 shows while recruiting

NCT06969261 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 4,656-participant average among 257 other Opioid Use Disorder trials with a reported enrollment target (100% lower).

The record links to 2 conditions, with Opioid Use Disorder appearing as the primary indexed condition, and to 1 intervention - of which Penny COPILOT is the first listed.

NCT06969261 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT06969261 about?

NCT06969261 is a clinical study titled "Adapting the Penny Chatbot for Perinatal OUD Patients: COPILOT". 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 COPILO...

What is the current status of trial NCT06969261?

This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2026-01-01. Estimated completion is 2026-06-30.

What conditions does trial NCT06969261 study?

This clinical trial studies the following conditions: Opioid Use Disorder, Perinatal Opioid Use Disorder.

What interventions are being tested in trial NCT06969261?

The interventions under investigation include: Penny COPILOT (BEHAVIORAL).

Who is sponsoring clinical trial NCT06969261?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06969261 being conducted?

This trial has 2 study locations across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Opioid Use Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06969261's enrollment target sits among peer trials

20 229th of 257 higher than 22 of 257 other Opioid Use Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Opioid Use Disorder 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 NCT06969261, the US trial registry maintained by the National Library of Medicine. NCT06969261 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.