Computerized Brief Intervention vs. Delayed Computerized Brief Intervention

NCT ID: NCT01936623

Last Updated: 2017-07-21

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-08-31

Study Completion Date

2014-09-30

Brief Summary

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The purpose of the study is to determine whether a computerized brief intervention for moderate risk drug use among adult primary care patients is more effective than providing such patients with a substance abuse assessment alone.

Detailed Description

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The study will enroll 80 adult primary care patients who have moderate risk drug use. Eligible participants (N = 80) will be randomly assigned to immediately receive a computerized brief intervention focused on drug use or to receive the same computerized brief intervention at 3-month follow-up. All participants will be assessed at three time points: baseline, and at 3 and 6 month follow-ups.

Conditions

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Drug Abuse

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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Computerized Brief Intervention

Computerized Brief Intervention is delivered using a talking, animated cartoon-like parrot that provides patient feedback, empathic reflection, and personalization regarding their drug use.

Group Type EXPERIMENTAL

Computerized Brief Intervention

Intervention Type BEHAVIORAL

No additional information needed.

Delayed Computerized Brief Intervention

Participants receive only a substance abuse assessment at baseline. At three-month follow-up, they then receive the computerized brief intervention.

Group Type OTHER

Computerized Brief Intervention

Intervention Type BEHAVIORAL

No additional information needed.

Interventions

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Computerized Brief Intervention

No additional information needed.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* (1) minimum 18 years of age
* (2) primary care or dental patients at the participating clinics
* (3) score between 4 and 26 (moderate-risk) for illicit drug and/or nonmedical use of prescription drugs on any of the single item drug use risk scores of the ASSIST.

Exclusion Criteria

* (1) score in the high-risk range on the ASSIST for any drug (except tobacco) or alcohol use (i.e., ASSIST score \> 26)
* (2) no reported drug use within the past 3 months
* (3) drug abuse treatment within the past 12 months
* (4) a BI at the clinic with the behavioral health counselor within the past month
* (5) prior enrollment in the parent study;
* (6) plans to move out of New Mexico in the next 6 months
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Friends Research Institute, Inc.

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Robert P Schwartz, M.D.

Role: PRINCIPAL_INVESTIGATOR

Friends Research Institute, Inc.

Locations

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First Choice Community Healthcare

Edgewood, New Mexico, United States

Site Status

Countries

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United States

Other Identifiers

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1R01DA026003

Identifier Type: NIH

Identifier Source: secondary_id

View Link

1R01DA026003-B

Identifier Type: -

Identifier Source: org_study_id

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