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Completed

NCT Number: NCT03457077

Neural and Mobile Assessment OF Behavior Change Among Problem Drinkers

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

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Key information

Age range

21 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

NYPInstitute

New York, 10032, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Brief intervention

Behavioral

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

Primary outcomes

  1. Drinking

    Time frame: 6 months

    Heavy drinking days

Sponsors and collaborators

Lead sponsor

New York State Psychiatric Institute

Other

Collaborators

  • Northwell Health

Registry information

Important dates

Study start
2018
Primary completion
2022
Study completion
2022
First posted
Mar 7, 2018
Registry last updated
Jul 5, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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