Motivational Interviewing Integrated With Social Network Counseling for Teens

NCT ID: NCT01922947

Last Updated: 2017-06-12

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

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-08-31

Study Completion Date

2014-11-30

Brief Summary

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The purpose of this research is to test the feasibility and efficacy of a brief (one session) preventative intervention using motivational interviewing integrated with social network counseling for substance use among adolescent patients in a primary care setting. One hundred participants will be randomly assigned to either motivational interviewing integrated with social network counseling or attention control conditions. The motivational interviewing integrated with social network counseling condition is expected to show improvement when compared to the attention control condition.

Detailed Description

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Conditions

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Substance Use

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Motivational Interviewing w/Social Network Counseling

Motivational Interviewing integrated with Social Network Counseling, 20-minute session.

Group Type ACTIVE_COMPARATOR

Active Control Condition

Intervention Type BEHAVIORAL

20-minute health counseling

Health Counseling

Group Type SHAM_COMPARATOR

Motivational Interviewing w/Social Network Counseling

Intervention Type BEHAVIORAL

This is the active arm of the study.

Interventions

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Motivational Interviewing w/Social Network Counseling

This is the active arm of the study.

Intervention Type BEHAVIORAL

Active Control Condition

20-minute health counseling

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 14-18 years old
* Resident of Richmond VA or greater Richmond area
* Patient at Virginia Commonwealth University or Richmond City Department of Health

Exclusion Criteria

* Ward of the state
* Not fluent in English
* Incapable of providing consent
Minimum Eligible Age

14 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

Virginia Commonwealth University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Michael P Mason, PhD

Role: PRINCIPAL_INVESTIGATOR

Virginia Commonwealth University

Locations

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Virginia Commonwealth University

Richmond, Virginia, United States

Site Status

Countries

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United States

Other Identifiers

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1R34DA032808-01A1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

HM14479

Identifier Type: -

Identifier Source: org_study_id

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