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| ID | Type | Description | Link |
|---|---|---|---|
| 1K23AA028295 | U.S. NIH Grant/Contract | View source | |
| 5R21AA026049 | U.S. NIH Grant/Contract | View source |
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The U.S. Department of Health and Human Services (HHS) Office of Human Research Protections (OHRP) issued an FWA restriction on NYSPI research that also included a pause of human subjects research as of June 23, 2023.
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| Name | Class |
|---|---|
| National Institute on Alcohol Abuse and Alcoholism (NIAAA) | NIH |
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The goal of this study is to investigate a treatment approach for alcohol use disorder (AUD) using a novel form of brain stimulation called deep repetitive transcranial magnetic stimulation (rTMS). The investigators will be targeting frontal regions of the brain that are important for memory and decision making. These brain regions have been shown to be impaired in patients with AUD. Previous studies have mostly used rTMS to a different frontal brain region that is not as deep. These studies have shown that rTMS can reduce craving for alcohol, but there is a lack of research showing that rTMS impacts alcohol consumption.
This study aims to examine the effect of rTMS on alcohol drinking behavior in an observed laboratory setting. Participants with AUD will be recruited and admitted to the inpatient unit for the whole study. After a brief detoxification period, they will receive 3 weeks of rTMS while in the research unit. Before and after the 3 weeks of stimulation, participants will participate in a decision-making experiment where they can choose to have an alcoholic drink or the equivalent amount of money that the drink would cost (alcohol self-administration sessions). The investigators will examine their response to alcohol, as well as their performance on tasks that relate to impulsivity and memory. Participants will also undergo an MRI scan (with spectroscopy) before and after the stimulation period to look at changes in the medial prefrontal cortex of the brain. Participants will then meet with a study physician for 6 weeks after the study for assessments of alcohol use and medical management sessions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Active Stimulation | Experimental | Participants will be receiving active rTMS. |
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| Sham Stimulation | Sham Comparator | Participants will be receiving sham stimulation with a smaller coil housed within the rTMS device. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| active rTMS | Device | rTMS delivers magnetic stimulation to the brain by using an electromagnet to generate a current that can penetrate the scalp and skull. |
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| Measure | Description | Time Frame |
|---|---|---|
| Change in the choice to self-administer alcohol in the laboratory as assessed by counting the number of drinks consumed in the 2-hour laboratory session. | Participants will participate in alcohol self-administration sessions in which they are presented with the choice of alcohol or money. The investigators will study the change in choices to choose alcohol during these sessions. There will be one session prior to rTMS and one after 3 weeks of rTMS. | 4 weeks |
| Number of Participants With Treatment-Related Adverse Events as Assessed by CTCAE v4.0. | Adverse events will be assessed in recorded in accordance with CTCAE v4.0. | 10 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in craving for alcohol measured using the Alcohol Urge Questionnaire (AUQ). | This AUQ (Bohn et al. 1995) is an 8-item self report questionnaire where participants rate a seven-point Likert scale with responses ranging from "strongly disagree" to "strongly agree", and a total score is derived from the sum of these items following reverse scoring of two items. A lower score is a better outcome which represents less desire to drink. Scores range from 8-56. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jonathan Wai | New York State Psychiatric Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| New York State Psychiatric Institute | New York | New York | 10032 | United States |
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| ID | Term |
|---|---|
| D000437 | Alcoholism |
| ID | Term |
|---|---|
| D019973 | Alcohol-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
| D001523 | Mental Disorders |
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active vs. sham stimulation
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double-blind
| Inpatient admission | Behavioral | All subjects will be admitted to the hospital for a brief detoxification period followed by 3 weeks of abstinence. |
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| sham rTMS | Device | The sham coil setting is designed to mimic the auditory artifact and the scalp sensations evoked by the real coil, and to produce activation of facial muscles similar to the effect of a real H coil, without stimulating the brain itself. |
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| 4 weeks |
| Change in GABA in the mPFC and ACC as measured with magnetic resonance spectroscopy (MRS). | MRS is performed by using an MRI machine to study metabolites and neurotransmitters in the brain. | 4 weeks |
| Change in abstinence from alcohol following discharge assessed with the Time Line Follow Back Interview. | 10 weeks |
| Changes in cognitive control as measured by using the Frontal Assessment Battery (FAB). | The FAB is a brief tool that discriminates between frontal-temporal type cognitive issues from from Alzheimer's type memory issues. Higher scores are better and scores range from 0-18. | 4 weeks |