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临床试验/NCT03595293
NCT03595293撤回不适用

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

Milton S. Hershey Medical Center0 个研究点目标入组 30 人开始时间: 2026年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
入组人数
30
主要终点
Improved capacity to increase neural activity in response to alcohol/pill cues in the rDLPFC measured by the change in the blood-oxygen level dependent (BOLD) signal

研究概览

简要总结

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".

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •sex: male or female
  • •Age: greater than or equal to 18 years
  • •Caron Treatment Center residential patients with alcohol use disorder, moderate to severe (equivalent to Alcohol Dependence in DSM-IV-TR), or prescription opioid use disorder (pOUD)
  • •Fluent in written and spoken English
  • •Patients who are right-handed
  • •Valid email address and reliable internet access after leaving the Caron Treatment Center

排除标准

  • •Patients who are concurrently receiving a psychoactive drug for the treatment of an Axis I disorder.
  • •Patients with current major depressive disorder or schizophrenia, bipolar disorder, post-traumatic stress disorder, or a history of traumatic brain injury.
  • •Decisional impairment
  • •Adults unable to consent
  • •Women who are pregnant
  • •Prisoners
  • •Patients who are left-handed
  • •No reliable email addresses

研究组 & 干预措施

Experimental Group for AUD Patients

Experimental

Patients will undergo six NFB sessions from the rDLPFC using a closed-loop fNIRs-based system. During each session, participants will walk through a maze on a computer screen three times. Each maze consists of alternating 30-second rest and 30-second active blocks. During each active block, the participant will come into visual contact with an alcohol image, blocking them from progressing through the maze. When patients encounter the alcohol image and they increase activity in their rDLPFC, the image in the maze will decrease in size and vice versa. The size of the alcohol image can fluctuate throughout each thirty second active block as the raw fNIRs signal from the rDLPFC will be sampled every 500 milliseconds using COBI studio software.

干预措施: fNIRs-based Neurofeedback (Device)

Sham Feedback Group for AUD Patients

Sham Comparator

Patients will undergo six sham feedback sessions from the skin over the zygomatic arch using a closed-loop fNIRs-based system. During each session, participants will walk through a maze on a computer screen three times. Each maze consists of alternating 30-second rest and 30-second active blocks. During each active block, the participant will come into visual contact with an alcohol image, blocking them from progressing through the maze. When participants encounter the alcohol image and they increase blood supply over the zygomatic area, the image will decrease in size and vice versa. The size of the alcohol image can fluctuate throughout each thirty second active block as the raw fNIRs signal from the zygomatic area will be sampled every 500 milliseconds using COBI studio software.

干预措施: Sham feedback (Device)

Experimental Group for pOUD Patients

Experimental

Patients will undergo six NFB sessions from the rDLPFC using a closed-loop fNIRs-based system. During each session, participants will walk through a maze on a computer screen three times. Each maze consists of alternating 30-second rest and 30-second active blocks. During each active block, the participant will come into visual contact with a pill image, blocking them from progressing through the maze. When patients encounter the pill image and they increase activity in their rDLPFC, the image in the maze will decrease in size and vice versa. The size of the pill image can fluctuate throughout each thirty second active block as the raw fNIRs signal from the rDLPFC will be sampled every 500 milliseconds using COBI studio software.

干预措施: fNIRs-based Neurofeedback (Device)

Sham Feedback Group for pOUD Patients

Sham Comparator

Patients will undergo six sham feedback sessions from the skin over the zygomatic arch using a closed-loop fNIRs-based system. During each session, participants will walk through a maze on a computer screen three times. Each maze consists of alternating 30-second rest and 30-second active blocks. During each active block, the participant will come into visual contact with a pill image, blocking them from progressing through the maze. When participants encounter the pill image and they increase blood supply over the zygomatic area, the image will decrease in size and vice versa. The size of the pill image can fluctuate throughout each thirty second active block as the raw fNIRs signal from the zygomatic area will be sampled every 500 milliseconds using COBI studio software.

干预措施: Sham feedback (Device)

结局指标

主要结局

Improved capacity to increase neural activity in response to alcohol/pill cues in the rDLPFC measured by the change in the blood-oxygen level dependent (BOLD) signal

时间窗: First two weeks of protocol

Increase in fNIRs signal response to pill/alcohol cues from pre-to-post neurofeedback sessions.

时间窗: First two weeks of protocol

Increase in neural activation in the rDLPFC when viewing alcohol cues from the first neurofeedback session to the sixth (last) session.

Higher levels of abstinence 90-days post-residential treatment completion as assessed by the 7-day timeline followback questionnaires.

时间窗: First 90 days after treatment completion at Caron Treatment Center

7-day timeline followback questionnaire will be sent out every week for 12 weeks to assess abstinence

次要结局

  • Change in self-reported self-efficacy from pre-to-post neurofeedback sessions assessed via the brief situational confidence questionnaire.(First two weeks of protocol)
  • Change in self-reported craving from pre-to-post neurofeedback sessions assessed via a 100-point craving visual analog scale.(First two weeks of protocol)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sue Grigson

Professor and Chair, Department of Neural and Behavioral Sciences

Milton S. Hershey Medical Center

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