Status:

RECRUITING

Longitudinal Neural Fingerprinting of Opioid-use Trajectories

Lead Sponsor:

Yale University

Collaborating Sponsors:

National Institute on Drug Abuse (NIDA)

Conditions:

Opioid Use Disorder

Eligibility:

All Genders

18-50 years

Phase:

NA

Brief Summary

This project aims to collect a densely sampled neuroimaging dataset among individuals receiving medications for opioid use disorder (MOUD). MOUD is multiphasic, comprised of medication induction, stab...

Detailed Description

MOUD individuals between the ages of 18 and 50 who recently enrolled in methadone treatment at APT Foundation clinics in the greater New Haven area. Investigators will aim to recruit individuals as ea...

Eligibility Criteria

Inclusion

  • within the first 6 months of methadone treatment for OUD and on a stable dose of methadone
  • eligibility for MRI scanning
  • willing to commit to longitudinal study visits

Exclusion

  • current psychosis, mania, or suicidal ideation with intent, as assessed during screening with the SCID-5
  • current co-occurring severe substance-use disorders (excluding nicotine and opioids), as assessed during screening with the SCID-5
  • current intoxication or acute withdrawal at time of study visit sufficient to prevent participation based on: behavioral observation, breathalyzer, and SOWS assessment (these individuals will be allowed to enroll at a later date once stable)
  • severe cognitive impairment (determined through consent process conducted by trained clinical research staff and during consent quiz or as indicated by a PROMIS Cognitive Function t-score \<30 (i.e., score indicating severe impairment)
  • Past or present history of intellectual disability or developmental disorder
  • Neurological disease (including seizures or epilepsy) as assessed by self-report and by consulting clinic records
  • Head trauma with loss of consciousness of more than 30 minutes
  • Organ dysfunction or any unstable or untreated medical conditions that may alter cerebral function or interfere with study participation

Key Trial Info

Start Date :

October 10 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2026

Estimated Enrollment :

10 Patients enrolled

Trial Details

Trial ID

NCT06207162

Start Date

October 10 2024

End Date

January 1 2026

Last Update

August 29 2025

Active Locations (1)

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1

MRRC at The Anlyan Center

New Haven, Connecticut, United States, 06520