Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT03595293

fNIRs-based Neurofeedback to Reduce Relapse in pOUD/AUD

Functional Near Infrared Spectroscopy-based Neurofeedback to Reduce Relapse in Prescription Opioid/Alcohol Use Disorders

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Milton S. Hershey Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study will examine the impact of functional near-infrared spectroscopy-based neurofeedback to a region within the brain's prefrontal cortex involved with self-regulation of resisting craving in alcohol use and prescription opioid use disorder patients. Participants will be asked to complete two cue reactivity tasks, six sessions of neurofeedback training as well as craving visual analog scales and self-efficacy questionnaires throughout a two-week period of their time in residential treatment at the Caron Treatment Center. They will be followed for 90 days after treatment completion at Caron to assess the impact neurofeedback had on their ability to remain sober once patients are living back in the "real world".

Conditions

Interventions

TypeNameDescription
DEVICEfNIRs-based NeurofeedbackPatients receive fNIRs-based neurofeedback from the rDLPFC to allow them to modify activation within this area.
DEVICESham feedbackPatients receive fNIRs-based sham feedback from the left zygomatic area to allow them to modify activation within this area.

Timeline

Start date
2026-01-01
Primary completion
2027-02-01
Completion
2028-02-01
First posted
2018-07-23
Last updated
2024-12-20

Source: ClinicalTrials.gov record NCT03595293. Inclusion in this directory is not an endorsement.

fNIRs-based Neurofeedback to Reduce Relapse in pOUD/AUD (NCT03595293) · Clinical Trials Directory