Using Telephone Technology to Prevent Relapse After Alcoholism Treatment

NCT ID: NCT00132795

Last Updated: 2012-06-21

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

PHASE2

Total Enrollment

158 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-05-31

Study Completion Date

2010-07-31

Brief Summary

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The purpose of this study is to determine whether a telephone based self-help program will prevent relapse among individuals undergoing standard substance abuse treatment.

Detailed Description

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Relapse rates in the first few months following substance abuse treatment are as high as 50%, in spite of the immediate effectiveness of treatments such as Cognitive Behavioral Therapy (CBT). Continuing use of therapy skills following treatment is associated with maintenance of treatment gains. We have programmed a telephone to deliver pre-recorded summaries and rehearsal sessions of skills learned in therapy. The system also includes monthly feedback messages from therapists. We expect that this ad-lib access to therapy skills would allow patients to generalize skills to their personal post-treatment lives. It would also allow individuals in remote or rural areas to obtain access to assistance without travel barriers.

Comparison(s): patients completing group CBT for substance abuse will be randomly assigned to two conditions. In one condition, patients will have unlimited access to the therapeutic telephone system for 4 months. The other condition is standard care (i.e., no formal relapse prevention).

Conditions

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Alcoholism

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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1 Therapeutic Phone System

patients assigned to this condition will have unlimited access to the therapeutic telephone system for 4 months.

Group Type EXPERIMENTAL

Daily monitoring of alcohol & drug use, & therapy skills

Intervention Type BEHAVIORAL

Comparison(s): patients completing group CBT for substance abuse will be randomly assigned to two conditions. In one condition, patients will have unlimited access to the therapeutic telephone system for 4 months. The other condition is standard care (i.e., no formal relapse prevention).

2 Standard care

Standard post-CBT care (i.e., no formal relapse prevention or professional treatment).

Group Type ACTIVE_COMPARATOR

control group

Intervention Type BEHAVIORAL

standard care (no added treatment)

Interventions

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Daily monitoring of alcohol & drug use, & therapy skills

Comparison(s): patients completing group CBT for substance abuse will be randomly assigned to two conditions. In one condition, patients will have unlimited access to the therapeutic telephone system for 4 months. The other condition is standard care (i.e., no formal relapse prevention).

Intervention Type BEHAVIORAL

control group

standard care (no added treatment)

Intervention Type BEHAVIORAL

Other Intervention Names

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relapse prevention

Eligibility Criteria

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Inclusion Criteria

* Meets current DSM-IV criteria for alcohol dependence
* Active drinking during the three months prior to entry into treatment
* Minimum age of 19
* Minimum sixth grade reading level.

Exclusion Criteria

* Meets criteria for a current psychotic illness
* Imminent plans to move or be incarcerated
* Presence of such severe hearing, visual, or cognitive deficit(s) that participation in CBT or use of an Interactive Voice Response (IVR) system are not possible
* Inability to identify at least one "locator" person to assist in tracking for follow-up assessments
* Does not have telephone service within the home
* Incarceration while in active protocol in the study
* Attendance of less than 8 of 12 CBT sessions
Minimum Eligible Age

19 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

University of Vermont

OTHER

Sponsor Role lead

Responsible Party

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John E. Helzer, MD

Professor of Psychiatry

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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John E. Helzer, MD

Role: PRINCIPAL_INVESTIGATOR

University of Vermont

Locations

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UVM Health Behavior Research Center

Burlington, Vermont, United States

Site Status

Countries

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United States

Related Links

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http://www.med.uvm.edu/hbrc/

Investigator's home page

Other Identifiers

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R01AA014270

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NIAAAHEL014270

Identifier Type: -

Identifier Source: org_study_id

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