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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03457077
Other study ID # 7390
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 27, 2018
Est. completion date December 31, 2022

Study information

Verified date July 2023
Source New York State Psychiatric Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will examine the neural mechanisms underlying both spontaneous behavior change and behavior change in response to a brief intervention among problem drinkers.


Description:

Although problem drinkers (PD) are a less severe, highly prevalent sub-type of alcohol use disorder (AUD) who are more likely to undergo reductions in alcohol use, compared to more severe AUD, the underlying mechanisms that maintain PD, as well as the mechanisms that underlie both spontaneous and treatment- related behavior change in this population, are not well understood. This proposal takes a lab to life approach by combining functional neuroimaging (fMRI), ecological momentary assessment (EMA), and brief interventions (BI) in non-treatment seeking PD to test whether heightened incentive salience (reactivity) to alcohol cues and impaired ability to regulate cue-induce craving are the mechanisms that characterize PD, and play a role in behavior change vs. persistence of behavior. Identifying these mechanisms is critical for testing and understanding treatments and uncovering who is most likely to respond to interventions.


Recruitment information / eligibility

Status Completed
Enrollment 164
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 55 Years
Eligibility Inclusion Criteria (Problem Drinkers): - Age 21-55 - English language fluency - Over the last 28 days ,Have an average weekly consumption of greater than 14 standard drinks for women, and greater than 24 standard drinks for men. - Current DSM-V mild or moderate alcohol use disorder (AUD) diagnosis - Own a smartphone with data plan Inclusion Criteria (Healthy Controls): - Age 21-55 - English language fluency - Have an average weekly consumption of less than </=14 standard drinks for women and less than/equal to 24 standard drinks for men and up to 2 heavy drinking days (>4/5 standard drinks for a woman/man) - No lifetime diagnosis of AUD - owns smartphone with a data plan Exclusion Criteria: - Past or current severe AUD as defined by DSM- V - Currently seeking treatment or attempting to stop drinking - Past or current alcohol withdrawal symptoms - Current DSM-V diagnosis of substance use disorder (other than nicotine or caffeine). - Regular use (more than 1-2 times weekly) of recreational drugs. - Psychotic Disorder or Bipolar disorder - Severe depression (Patient Health Questionnaire score > 19) or anxiety (Beck Anxiety Inventory > 25) - Substantial risk of suicide or violence - MRI contraindications (e.g., metallic implants, pacemaker, weight > 350 lbs, waist > 55") - Hearing impaired/hearing aids, unable to read newspaper at arm's length with corrective - Objective cognitive impairment - Current or recent (evidence of disease x 5 years) non-skin neoplastic disease or melanoma. - Active hepatic disease (not a history of hepatitis) or primary renal disease requiring dialysis, primary untreated endocrine diseases, e.g., Cushing's disease or primary hypothalamic failure or insulin dependent diabetes (Type I or II). Well-treated hypothyroidism will not be excluded. - Pregnant, lactating (participation allowed 3 months after ceasing lactation), or currently intending to become pregnant - Any history of ECT - Brain disorder such as stroke, tumor, infection, epilepsy, multiple sclerosis, degenerative diseases, head injury (LOC > 5 minutes), mental retardation - Diagnosed learning disability, dyslexia, or ADHD - For women: Current pregnancy or intention to be pregnant in the near future

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Brief intervention
A brief motivational intervention with feedback about drinking levels compared to norms

Locations

Country Name City State
United States NYPInstitute New York New York

Sponsors (2)

Lead Sponsor Collaborator
New York State Psychiatric Institute Northwell Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Drinking Heavy drinking days 6 months
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