Actively Recruiting

Age: 18Years - 60Years
All Genders
NCT06136247

Integrating Brain, Neurocognitive, and Computational Tools in OUD

Led by University of Pennsylvania · Updated on 2025-12-04

192

Participants Needed

1

Research Sites

195 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The 5-year K01 Mentored Research Scientist proposal will employ brain, neurocognitive, and computational tools (e.g., machine learning) to understand the impact of opioid-use disorder (OUD) and common co-occurring issues on executive function and clinical outcomes. There have been record numbers of fatal and non-fatal overdoses (ODs) associated with opioids (and other drugs) in the past 12-months. Improving classification and predictive capabilities to enhance treatment and prevent relapse is of the upmost importance. Deficits in neurocognition often are associated with poor treatment outcomes (e.g., more drug use, medication non-adherence), yet co-occurring issues associated with OUD (e.g., depression, anxiety, physical/sexual abuse, neglect) make it difficult to parse which contributing factors lead to worse executive function (EF) and poorer treatment outcomes. Novel brain, neurocognitive, and computational tools are needed to help determine these differences, in order to lay the foundation for better treatments. This need has shaped both the training plan and the associated research project in a 5-year K01 Mentored Research Scientist proposal, building on Dr. Regier's prior preclinical and clinical addiction neuroscience experience (focused mostly on cocaine-use disorders, cue-reactivity, subcortical networks, prior adversity, and univariate imaging techniques).

CONDITIONS

Official Title

Integrating Brain, Neurocognitive, and Computational Tools in OUD

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women with moderate to severe opioid use disorder by DSM-V criteria on a stable (at least one week without change) dose of oral buprenorphine-naloxone or methadone
  • Age between 18 and 60 years
  • Able to read at an eighth-grade level
  • Able to speak English
Not Eligible

You will not qualify if you...

  • Unable to understand or complete the study tasks
  • Certain mental health conditions that interfere with participation, including bipolar I with current manic episode, schizophrenia, and schizoaffective disorder as determined by the Principal Investigator
  • Moderate or severe substance-use disorder for healthy control participants

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

P

Paul Regier, PhD

CONTACT

M

Megan Ivey, MS

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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