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Completed

NCT Number: NCT01642381

Component Analysis for Motivational Interviewing

The purpose of this study is to investigate the critical components of motivational interviewing (MI), a psychotherapeutic intervention, in reducing heavy or problematic drinking. The study will disaggregate MI into its component parts and test full MI compared to MI without its directive strategies. This study will test whether the directive elements of MI are critical or whether MI effects may be attributable solely to its Rogerian, non-directive components. For more information, go to http://caspirnyc.org/p_motion.html

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

North Shore LIJ Health Systems

Great Neck, New York, 11021, United States

About this study

Project Motion is a clinical research study for people seeking to reduce, but not stop their drinking. Individuals who qualify will receive a comprehensive assessment and brief individual psychotherapy at no cost. The study is being conducted by a team of scientists at Columbia University College of Physicians and Surgeons and the New York State Psychiatric Institute and is funded by the National Institutes of Health (NIH). Our offices are located next to Columbus Circle and we offer convenient hours for appointments.

The purpose of our study is to understand how brief psychotherapy helps people reduce alcohol consumption and drinking problems. For example, we know that some people can reduce drinking with little or no treatment, whereas others benefit from one-on-one psychotherapy. However, we do not know why this happens. Individuals who qualify and decide to participate will be assigned by chance to one of three conditions. Individuals assigned to the first two conditions will receive brief psychotherapy, beginning the first week of their participation in the study. Individuals in the third condition will receive feedback on their drinking and be asked to reduce their drinking with the aid of telephone self-monitoring for a period of 8 weeks. Individuals in the third condition will then receive psychotherapy as well. The delay of 8 weeks will allow us to understand how the psychotherapy works compared to how people change without counseling.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Primary current diagnosis of Alcohol Use Disorder
  • Meets DSM-IV criteria for inability to control or cut down on drinking
  • Have an average weekly consumption of >24 standard drinks for men and >15 standard drinks for women
  • Show no evidence of significant cognitive impairment
  • Are willing to reduce drinking to non-hazardous levels
  • Not seeking to quit drinking
  • Agree not to seek additional substance abuse treatment during treatment period
  • Fluent in English

Exclusion criteria

  • Have a current DSM-IV diagnosis of drug dependence (other than nicotine/marijuana)
  • Have a serious psychiatric illness (e.g., psychotic disorder, bipolar disorder, major depression) or substantial suicide or violence risk
  • Have clinically severe alcoholism as evidenced by a history of significant medical problems associated with drinking, seizures or severe withdrawal symptoms, or an inpatient treatment episode for drinking
  • Legally mandated to receive substance abuse treatment
  • Sufficiently socially unstable as to preclude completion of study requirements (e.g., homeless)

Treatment and study plan

Full Motivational Interviewing ("FMI")

Behavioral

Relational and technical technical (directive) strategies in counselling sessions to significantly increase commitment strength to reduce drinking.

Spirit Only Motivational Interviewing ("SOMI")

Behavioral

Empathic and non-directive counselling based on Rogerian psychotherapy model.

Primary outcomes

  1. Time Line Follow Back

    Time frame: 36 weeks

    Calendar-based method of recording drinking patterns. Data will be aggregated into summary variables including sum of standard drinks, mean drinks per drinking day, and percent days heavy drinking at multiple time points.

Sponsors and collaborators

Lead sponsor

Northwell Health

Other

Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Registry information

Important dates

Study start
2012
Primary completion
2016
Study completion
2016
First posted
Jul 17, 2012
Registry last updated
Sep 12, 2016

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.

Published trials that share one or more normalized conditions with this study.