Dental and Medical Office iMET to Reduce Teen Tobacco, Alcohol, and Drug Use

NCT ID: NCT00907309

Last Updated: 2016-10-07

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

PHASE1/PHASE2

Total Enrollment

121 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-09-30

Study Completion Date

2012-09-30

Brief Summary

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The purpose of the project is to improve adolescent behavioral counseling services in healthcare settings with a new Internet/Intranet-based Motivational Enhancement Therapy (iMET) intervention that targets the use of tobacco, alcohol, and other drugs.

Detailed Description

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We have previously developed and tested in a treatment population a promising MET program for alcohol and drug use. We will broaden the MET intervention to also target tobacco use and convert the new materials into a self-administered format.

Conditions

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Use; Tobacco, Harmful Alcohol Abuse Drug 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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Treatment as usual

Participants will receive treatment as usual from their provider.

Group Type NO_INTERVENTION

No interventions assigned to this group

iMET

Participants will receive the iMET intervention.

Group Type EXPERIMENTAL

iMET

Intervention Type BEHAVIORAL

Participants will receive the iMET intervention

iMET/TE

Participants will receive the iMET intervention and Technological Extenders (TEs).

Group Type EXPERIMENTAL

iMET/TE

Intervention Type BEHAVIORAL

Participants will receive the iMET intervention and also receive TEs (Technological Extenders)

Interventions

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iMET

Participants will receive the iMET intervention

Intervention Type BEHAVIORAL

iMET/TE

Participants will receive the iMET intervention and also receive TEs (Technological Extenders)

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* 12-21 years old
* Coming for routine care

Exclusion Criteria

* Medically or emotionally unstable day of visit
* Already receiving behavioral health services
* Cannot read/understand English
* Will not be available for post-tests
Minimum Eligible Age

12 Years

Maximum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cambridge Health Alliance

OTHER

Sponsor Role collaborator

Tufts Medical Center

OTHER

Sponsor Role collaborator

Harvard School of Dental Medicine

OTHER

Sponsor Role collaborator

Fallon Clinic

INDUSTRY

Sponsor Role collaborator

Boston Children's Hospital

OTHER

Sponsor Role lead

Responsible Party

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John R Knight, MD

Associate Professor of Pediatrics, Harvard Medical School; Senior Associate in Medicine; Associate in Psychiatry, Director, Center for Adolescent Substance Abuse Research, Boston Children's Hospital

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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John R. Knight, MD

Role: PRINCIPAL_INVESTIGATOR

Boston Children's Hospital

Locations

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Children's Hospital Boston

Boston, Massachusetts, United States

Site Status

Countries

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United States

References

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Holliday R, Hong B, McColl E, Livingstone-Banks J, Preshaw PM. Interventions for tobacco cessation delivered by dental professionals. Cochrane Database Syst Rev. 2021 Feb 19;2(2):CD005084. doi: 10.1002/14651858.CD005084.pub4.

Reference Type DERIVED
PMID: 33605440 (View on PubMed)

Related Links

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http://www.ceasar.org

web site of Center for Adolescent Substance Abuse Research at Children's Hospital Boston

Other Identifiers

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iMET RFA-OD-09-003

Identifier Type: -

Identifier Source: org_study_id

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