Clinical Trials Logo

Substance-Related Disorders clinical trials

View clinical trials related to Substance-Related Disorders.

Filter by:

NCT ID: NCT02907944 Completed - Clinical trials for Substance-related Disorders

Working With HIV Clinics to Adopt Addiction Treatments Using Implementation Facilitation

WHAT-IF?
Start date: September 2016
Phase: N/A
Study type: Interventional

Tobacco, alcohol and opioid use disorders threaten the health of HIV-infected patients. What if evidence-based counseling and medication treatments for tobacco, alcohol and opioid use disorders (herein refered to as addiction treatments) were routinely provided in HIV clinics? Implementation Facilitation is an established strategy to increase the uptake of evidence-based treatments. Our goal is to evaluate the impact of Implementation Facilitation on the use of addiction treatments in four large HIV clinics. The purpose of the WHAT-IF study is: Aim 1. Among key stakeholders, to use quantitative and qualitative (mixed) methods to identify the site-specific evidence, context and facilitation-related barriers and facilitators to the integration of addiction treatments to help tailor an Implementation Facilitation for each clinic. Aim 2. To evaluate the impact of Implementation Facilitation on: 2a: Organizational readiness to deliver addiction treatments 2b: Provider readiness to deliver addiction treatments 2c: Provision of addiction treatments 2d: Changes in organizational models of care used to deliver addiction treatments Aim 3. To evaluate the impact of Implementation Facilitation on antiretroviral therapy receipt, HIV viral suppression, VACS Index, and retention in HIV care among patients eligible for addiction treatment.

NCT ID: NCT02907697 Active, not recruiting - HIV Clinical Trials

Adherence Intervention for HIV-infected Drug Users

Start date: January 1, 2016
Phase: N/A
Study type: Interventional

Many people living with HIV use illicit drugs, which leads to worsened health outcomes and increased transmission of HIV due to poor adherence to medication regimens. This research will develop an intervention targeting medication adherence that is tailored to the unique needs of HIV-infected drug users. This research will promote adherence and improve treatment outcomes among HIV-infected drug users thereby minimizing the development of drug resistant strains of HIV and reducing transmission.

NCT ID: NCT02906215 Completed - HIV Clinical Trials

Mobile Application to Improve Care Coordination Among HIV Clinic and Substance Use Treatment Providers

Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Many people living with HIV use illicit drugs and require treatment for both HIV and drug use, however, many barriers exist which prevent integration of dual care services. This study will develop a novel intervention aimed at the provider-level which will combine an evidence-based training model with use of mobile technology to improve care coordination between providers at HIV clinics and substance use treatment facilities. If proven effective, this intervention may be widely disseminated and easily implemented into existing clinic structures, thereby improving care coordination among providers and linkage to dual treatment for HIV-infected people who use drugs.

NCT ID: NCT02903251 Completed - Clinical trials for Substance-Related Disorders

Oxytocin and Alcohol Withdrawal and Dependence

Start date: October 2016
Phase: Phase 3
Study type: Interventional

This study evaluates the effect of oxytocin nasal spray on alcohol withdrawal and dependence in adults admitted for detoxification of alcohol, and during the following 4 weeks in an outpatient setting. Half of the participants will receive oxytocin nasal spray, the other half placebo nasal spray.

NCT ID: NCT02902081 Completed - Drug Addiction Clinical Trials

Cannabidiol and Emotional Stimuli

CAS
Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of this research is to examine the effect of cannabidiol (CBD), a cannabinoid compound found in marijuana, on responses to emotional stimuli. Both preclinical and clinical studies indicate that CBD may act to reduce anxiety without excessive sedative side-effects. Thus the investigators hypothesize that CBD may reduce responses specifically to negative emotional and social stimuli, including pictures and emotional faces, without altering responses to positive stimuli. To examine this, the investigators will administer placebo, 300mg, 600mg, and 900mg CBD to healthy normal adults in a double-blind within-subjects study. The investigators will measure subjective and subtle physical responses to positive and negative stimuli using measures that have been characterized with classic anxiety-reducing drugs and drugs of abuse. Further, the investigators will examine whether CBD-induced changes in these measures of emotional response relate to changes in actual behavior in a controlled social interaction. These results will allow the investigators to examine the potential usefulness of CBD as an anxiety-reducing drug, and suggest mechanisms by which CBD may reduce anxiety.

NCT ID: NCT02894476 Recruiting - Alcoholism Clinical Trials

Substance Dependence Satisfaction With Care and Quality Of Life

SUBUSQOL
Start date: April 2014
Phase: N/A
Study type: Observational

The SUBUSQOL cohort aimed to improve knowledge of the quality of ambulatory care, in particular the prognostic role of the early satisfaction with care on the change from baseline quality of self-reported health status in outpatients with alcohol or opioid dependence. It is a multicenter prospective cohort. Satisfaction was assessed using a multidimensional self-administered and validated questionnaire during the early care process. In addition to measuring satisfaction and obtaining sociodemographic and clinical data, this study collected data on the self-reported health status at inclusion and 3, 6 and 12 months after inclusion.

NCT ID: NCT02892110 Completed - Clinical trials for Substance Use Disorder

Varenicline Treatment for Cannabis Use Disorder

Start date: February 13, 2017
Phase: Phase 2
Study type: Interventional

Marijuana is the most commonly used illicit drug. There is high demand for effective interventions for cannabis use disorder, yet few specific treatments for have been developed. This study will evaluate the efficacy of varenicline for reducing marijuana use in people who use marijuana frequently.

NCT ID: NCT02888249 Completed - Clinical trials for Tobacco Use Disorder

Behavioral Economic Purchasing Decisions for Cigarettes of Varied Compositions

Start date: August 25, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the abuse liability of cigarettes with altered composition (cigarettes differing in composition; e.g., tar levels, amount of sugar, casings) is reduced relative to standard composition cigarettes.

NCT ID: NCT02872467 Completed - Pregnancy Clinical Trials

Prenatal Cocaine, Nasal Oxytocin, and Maternal Psychophysiology

NOX
Start date: May 2016
Phase: Phase 1
Study type: Interventional

The purpose of this research is to study the effects of nasal oxytocin administration on maternal behaviors that may be influenced by cocaine use during pregnancy. 32 mothers with prenatal use of cocaine during the current pregnancy will be studied at 3-6 months postpartum, when they will complete 3 study visits, a 2-week double-blind trial of twice daily nasal spray (oxytocin or placebo) and 4 telephone interviews. All information collected is confidential.

NCT ID: NCT02871232 Enrolling by invitation - Clinical trials for Opioid-related Disorders

Surveillance Monitoring of Opioid Abuse in Poison and Drug Treatment Centers

Start date: n/a
Phase: N/A
Study type: Observational

To conduct surveillance for abuse, misuse, overdose, addiction, and death and to evaluate if the REMS meets its surveillance goals, and if it does not, to modify it appropriately based on the metrics. Briefly, therefore, the overall surveillance objective is to evaluate for trends before and after the shared REMS is implemented to collectively assess for changes in abuse, misuse, overdose, addiction, and death for different risk groups and settings.