- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00033124
A Behavioral Trial for the Treatment of Methamphetamine Dependence. - 1
January 10, 2017 updated by: National Institute on Drug Abuse (NIDA)
Behavioral Trial for the Treatment of Methamphetamine Dependence
The purpose of this study is to examine behavioral treatment for methamphetamine dependence.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
To characterize meth.
withdrawal symptoms using a multidimensional withdrawal questionnaire; to field test and investigate the effect of using an algorithm developed for discriminating between new use and residual carry-over of meth metabolites in urine and to evaluate the treatment response of meth.
users to participation in the thrice weekly psychosocial protocol to be used as a "platform" in future pharmacotherapy trials.
Study Type
Interventional
Enrollment
50
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Chula Vista, California, United States, 91911
- South Bay Treatment Center
-
Costa Mesa, California, United States, 92627
- Matrix Institute on Addictions
-
-
Hawaii
-
Honolulu, Hawaii, United States, 96813
- John A. Burns School of Medicine
-
-
Iowa
-
Des Moines, Iowa, United States, 50316
- Powell Chemical Dependency Center
-
-
Missouri
-
Independence, Missouri, United States, 64052
- Comprehensive Mental Health Services, Inc
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
Male or Female at least 18 yrs of age; DSM-4 diagnosis of methamphetamine (METH) dependence; be willing to comply with study procedures; verbalize understanding of consent and provide written consent and willingness to complete study procedures; be seeking treatment for METH dependence.
Exclusion Criteria:
Additional criteria available during screening at the site.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
Withdrawal symptoms
|
New Use algorithm
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Richard Rawson, Ph.D., National Institute on Drug Abuse (NIDA)
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2001
Study Completion
June 1, 2002
Study Registration Dates
First Submitted
April 5, 2002
First Submitted That Met QC Criteria
April 5, 2002
First Posted (Estimate)
April 8, 2002
Study Record Updates
Last Update Posted (Estimate)
January 11, 2017
Last Update Submitted That Met QC Criteria
January 10, 2017
Last Verified
August 1, 2003
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NIDA-CTO-0009-1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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