Viewing Study NCT00218192



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Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00218192
Status: COMPLETED
Last Update Posted: 2015-05-22
First Post: 2005-09-16

Brief Title: A Trial to Reduce Hepatitis C Among Injection Drug Users - 1
Sponsor: Butler Hospital
Organization: Butler Hospital

Study Overview

Official Title: A Trial to Reduce Hepatitis C Among Injection Drug Users
Status: COMPLETED
Status Verified Date: 2013-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to examine the efficacy of a brief motivational intervention on the cumulative incidence of Hepatitis C
Detailed Description: Injection drug users are at high risk for blood-borne viral infections during their first years of injecting when they are least likely to seek formal substance abuse treatment and are likely to be practicing risky drug-use behaviors Research has demonstrated that a brief motivational intervention that includes booster sessions and addresses drug and sex risks is effective in reducing HIV risk behaviors among injection drug users

Because Hepatitis C Virus is a bloodborne pathogen like HIV and transmission occurs via similar behaviors successful HIV prevention strategies should be robust in preventing HCV but need to be tested Motivational interventions which aim to elicit a goal and plan from the patient to reduce injection and sexual risk taking are particularly suited to address behaviorally-based changes Motivational interventions are individualized and tailored to the risks and concerns of the participant but can be standardized and evaluated to make this technique applicable in a variety of settings The occurrence of injection drug use in a population with traditionally poor linkage to primary care an enormous burden of illness and high HCV and other blood-borne pathogen transmission risk supports the use of motivational interventions in this group

Comparisons Participants are assigned in this 24 month longitudinal study to an assessment-only condition or an assessment plus motivational intervention condition Participants in the intervention condition receive up to 4 sessions of motivational interviewing during the first 6 months of the study

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
R01DA013759 NIH None None
R01-13759-1 US NIH GrantContract None httpsreporternihgovquickSearchR01DA013759