Component Analysis for Motivational Interviewing

NCT ID: NCT01642381

Last Updated: 2016-09-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

139 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-05-31

Study Completion Date

2016-08-31

Brief Summary

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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

Detailed Description

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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.

Conditions

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Alcohol-Related Disorders Alcohol Use Disorders Alcohol Drinking Alcoholism Alcohol Abuse

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Psychotherapy

Group Type ACTIVE_COMPARATOR

Full Motivational Interviewing ("FMI")

Intervention Type BEHAVIORAL

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

Spirit Only Motivational Interviewing ("SOMI")

Intervention Type BEHAVIORAL

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

Self-Change Control ("SCC")

SCC participants will be told that they should attempt to reduce their drinking over the course of 8 weeks. (If unsuccessful, they will be offered Full Motivational Interviewing therapy sessions.)

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Full Motivational Interviewing ("FMI")

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

Intervention Type BEHAVIORAL

Spirit Only Motivational Interviewing ("SOMI")

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

Intervention Type BEHAVIORAL

Eligibility Criteria

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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)
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Alcohol Abuse and Alcoholism (NIAAA)

NIH

Sponsor Role collaborator

Northwell Health

OTHER

Sponsor Role lead

Responsible Party

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Jonathan Morgenstern

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jonathan Morgenstern, PhD

Role: PRINCIPAL_INVESTIGATOR

North Shore LIJ Health Systems

Locations

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North Shore LIJ Health Systems

Great Neck, New York, United States

Site Status

Countries

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United States

Other Identifiers

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AA 020077-01A1

Identifier Type: -

Identifier Source: org_study_id

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