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Substance-Related Disorders clinical trials

View clinical trials related to Substance-Related Disorders.

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NCT ID: NCT00252512 Completed - Clinical trials for Substance Use Disorders

The Effect of a Contingency Management Intervention on Substance Use

REAP
Start date: May 2007
Phase: N/A
Study type: Interventional

Contingency management interventions involve providing a tangible reward for progress toward treatment goals. The purpose of this study is to determine whether a contingency management intervention added to usual care leads to improved attendance and decreased substance use in patients attending outpatient substance use disorders treatment.

NCT ID: NCT00249756 Completed - Clinical trials for Substance-Related Disorders

Re-Entry MTC for Offenders With MICA Disorders

Start date: August 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the transition of offenders with both mental illness and chemical abuse (MICA) disorders from prison to the community, where continued treatment is generally considered necessary to sustain gains made by prison treatment, and to achieve successful outcomes. The project will determine the effectiveness of a modified therapeutic community (Re-Entry MTC) approach as compared to the case management and parole supervision currently provided. The study will also assess the relative impact on treatment outcomes of the type of treatment received while in prison and of the progress achieved in re-entry treatment.

NCT ID: NCT00249717 Completed - Substance Abuse Clinical Trials

Group-Based Contingency Management for Substance Abuse Treatment - 1

Start date: May 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of prize-based contingency management (CM) when administered exclusively in groups. Substance dependent patients (N=360) at community-based treatment programs are randomly assigned to one of two conditions: (a) standard, non-CM treatment or (b) standard treatment plus prize CM delivered in groups. In the CM condition, patients earn the opportunity to win prizes for attending groups and submitting drug-free biological specimens. Substance use and psychosocial problems are measured at intake, month 1, month 3 (post treatment), and at 6-, 9-, and 12-month follow-up evaluations. We also assess patient characteristics that may be associated with improved outcomes within and across conditions.

NCT ID: NCT00249665 Completed - Clinical trials for Substance-Related Disorders

Perindopril-Methamphetamine Interaction Study

Start date: August 2004
Phase: Phase 1/Phase 2
Study type: Interventional

Due to its ease of synthesis and powerful psychostimulant effects, abuse of methamphetamine has increased rapidly over the last decade. No medications are currently approved for the treatment of methamphetamine dependence or withdrawal. The purpose of this study is to determine whether perindopril, an angiotensin converting enzyme (ACE) inhibitor, modifies cardiovascular responses and adverse events when taking methamphetamines.

NCT ID: NCT00249652 Completed - Clinical trials for End Stage Renal Disease

Transplant and Addiction Project (TAP) - 1

Start date: September 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test a novel distance-based (telephone) intervention to help transplant candidates with current or recent substance abuse to stay "clean and sober" both prior and following transplant surgery.

NCT ID: NCT00249639 Completed - Substance Abuse Clinical Trials

Contingency Management for Attendance - 2

Start date: January 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of a low-cost contingency management procedure as compared to standard treatment. Using a cross-over design, CM is implemented at different community-based clinics and compared with non-CM in the same facilities. Research staff collects information regarding patients' demographic characteristics, attendance, and outcomes at the clinics. During Phase A (non-CM), standard clinical practice is in place. During Phase B (CM), all patients have the chance to win prizes by coming to treatment. Each participating clinic is randomly assigned to receive either the A or B phase first; each phase is in effect for 16 weeks.

NCT ID: NCT00249613 Completed - Clinical trials for Substance Abuse Problem

Gender-Responsive Treatment for Women Offenders - 1

Start date: June 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether substance abuse treatment designed specifically for drug-dependent women offenders provides better outcomes than standard drug court treatment (mixed-gender programs).

NCT ID: NCT00249561 Completed - Clinical trials for Substance-Related Disorders

Colorado Women's TC Project

Start date: September 2001
Phase: Phase 1/Phase 2
Study type: Interventional

The major aim of the project is to document and evaluate two treatments for female offenders with substance abuse problems (TC and cognitive behavioral), simultaneously studying the process of treatment, and relating treatment process to treatment outcome.

NCT ID: NCT00249548 Completed - Substance Abuse Clinical Trials

Low-Cost Contingency Management for Hispanic Outpatients - 3

Start date: August 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of a lower-cost contingency management (CM) procedure in Hispanic substance abusing outpatients. Thirty individuals meeting DSM-IV criteria for substance dependence receive one of two conditions: (a) standard treatment, or (b) standard treatment plus prize CM. Using a cross-over design, CM is implemented in a community-based outpatient clinic and compared with non-CM in the same clinic. The participating clinic is randomly assigned to receive either the CM or non-CM phase first; 15 weeks after the final participant in one phase is enrolled, a one-week washout period occurs, followed by a switch to the other phase. Patients initiating outpatient treatment during the non-CM phase receive standard treatment and submit urine and breath samples 2/week during Weeks 1-6 and 1/week during Weeks 7-12. Patients initiating treatment during the CM phase also receive standard treatment and the same breath and urine monitoring. In addition, they earn the opportunity to win prizes for coming to treatment and for submitting negative breath and urine samples. Follow-up interviews are conducted at 1,3,6 and 9 months following intake during which substance use and psychosocial functioning are assessed.

NCT ID: NCT00249522 Completed - Substance Abuse Clinical Trials

Vouchers vs. Prizes for Methadone Patients - 1

Start date: August 2003
Phase: N/A
Study type: Interventional

The purpose of this study is to compare voucher-based contingency management (CM) procedures to a lower-cost CM system that provides opportunities to win prizes. Cocaine-dependent outpatients are randomly assigned to (a) standard treatment, (b) standard treatment plus voucher CM for abstinence, defined by negative breath and urinalysis test results, or (c) standard treatment plus prize CM for abstinence, defined by negative breath and urinalysis test results. Urine and breath samples are collected 3x/week during Weeks 1-3, 2x/week during Weeks 4-6 and 1x/week during Weeks 7-12. Follow-up interviews are conducted 1,3,6 and 9 months following intake during which substance use and psychosocial functioning are assessed.