Development of a Family-Based Treatment for Adolescent Methamphetamine Use

NCT ID: NCT00680511

Last Updated: 2014-08-05

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-09-30

Study Completion Date

2013-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The AIMS study compares a methamphetamine-specific treatment intervention to a treatment-as-usual Functional Family Therapy (FFT) approach for adolescents ages 15 to 19. Adolescents are assigned to one of two treatment conditions: (1) 16 weeks of FFT designed to strengthen family relationships and develop skills for helping the adolescent avoid drug use; or (2) 16 weeks of a combination of FFT and a methamphetamine-specific intervention involving group and individual therapy sessions; Families are assessed using questionnaires and interviews, and adolescents participate in neuropsychological testing, before, during, and after treatment to provide information about family functioning, the adolescent's drug use, the adolescent's peers, and other factors that may contribute to treatment success. Adolescents also provide urine specimens for drug screening at assessment visits. Through a partnership with Oregon Health and Science University (OHSU), adolescents will participate in functional magnetic resonance imaging appointments at the hospital to examine regional brain blood flow during tasks designed to measure impulsivity and risk-taking behaviors. As a treatment development grant, study investigators will study adolescents' acceptance of and response to the newly developed methamphetamine-specific treatment approach.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Behavior and Mental Disorders Methamphetamine Disorders

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

1

Family therapy combined with methamphetamine-specific group treatment.

Group Type ACTIVE_COMPARATOR

Adolescent Methamphetamine Treament (AMT)

Intervention Type BEHAVIORAL

AMT Group Therapy plus Functional Family Therapy (FFT)

2

Family Therapy.

Group Type ACTIVE_COMPARATOR

Functional Family Therapy (FFT)

Intervention Type BEHAVIORAL

FFT

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Adolescent Methamphetamine Treament (AMT)

AMT Group Therapy plus Functional Family Therapy (FFT)

Intervention Type BEHAVIORAL

Functional Family Therapy (FFT)

FFT

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 15 to 19 years of age.
* Have at least one parent or parent figure willing to participate.
* Meet DSM-IV diagnostic criteria for drug-abuse or dependence, including a specific meth use disorder.
* Reports meth use on at least 5 of the previous 90 days.
* Have contact with the parent on at least 40% of the past 90 days.
* With their parent be willing to accept randomization to one of the two treatment interventions.
* Be willing to participate in the imaging task in the fMRI pilot study.
* Have basic English competency.
* Have sufficient residential stability to permit probable contact at follow-up.

Exclusion Criteria

* Evidence of psychotic or organic state of sufficient severity to interfere with understanding of study instruments and procedures.
* Have a medical or psychological condition that would preclude undergoing the fMRI scan.
* Have a sibling who is participating in the study.
Minimum Eligible Age

15 Years

Maximum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

Oregon Research Institute

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Holly B. Waldron, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Oregon Research Institute

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Oregon Research Institute Center for Family and Adolescent Research

Portland, Oregon, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

DA021695

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.