Substance Abuse Pre-Treatment Screening Study

Status Recruiting

Clinical Trial Summary

The overarching goal of this project is to have a consolidated consent and evaluation procedure that will lead potential subjects to the most appropriate clinical trial or human laboratory study (and its consent process) for their presenting concerns or interests. A second purpose is to have a consolidated intake data base on which secondary analyses can be conducted.

Clinical Trial Description

Approximately 1500 candidates per year will respond to advertisements and will complete preliminary telephone screening without identifiers. Appropriate candidates will be given appointment times and on arrival will undergo the consent process for evaluation. A complete medical, social, psychiatric, and drug use history will be obtained. Subjects fulfilling general health inclusion requirements will then be offered an appropriate study for which the specific consent will be obtained. The evaluation period will be no more than one day with all results evaluated within the two following days. Acceptable candidates will then be invited to complete the study specific consent. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00439049
Study type	Observational
Source	The University of Texas Health Science Center, Houston
Contact	Jessica Vincent, BS
Phone	713-486-2803
Email	Jessica.N.Vincent@uth.tmc.edu
Status	Recruiting
Phase
Start date	October 2005
Completion date	June 2026

View Details

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