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Alcohol Abuse clinical trials

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NCT ID: NCT03655574 Active, not recruiting - Substance Abuse Clinical Trials

Substance Use Interventions for Truant Adolescents

GOALS
Start date: January 1, 2019
Phase: N/A
Study type: Interventional

This study evaluates a brief motivation-building intervention for parents and teens to reduce truancy and substance use. It is hypothesized that the motivational intervention will result in better outcomes compared to an education-only intervention.

NCT ID: NCT03247647 Active, not recruiting - Alcohol Abuse Clinical Trials

Personal Values and Mandated Students

Start date: March 13, 2018
Phase: N/A
Study type: Interventional

This study aims to examine the efficacy of an enhanced alcohol intervention among individuals who are mandated to complete an alcohol education activity as part of a university sanction.

NCT ID: NCT02984241 Active, not recruiting - Alcohol Abuse Clinical Trials

e-Health Coping Skills Training for Women Whose Partner Has a Drinking Problem

Start date: October 13, 2019
Phase: N/A
Study type: Interventional

This study evaluates web-based interventions to help women cope with the stress arising from living with a problem-drinking partner

NCT ID: NCT02873663 Active, not recruiting - Alcohol Abuse Clinical Trials

Biomarkers for the Detection of Heavy Alcohol Use in Patients With and Without Liver Disease

Start date: December 2010
Phase: N/A
Study type: Interventional

The investigators will test the validity of biomarkers for the detection of heavy alcohol use in patients with and without liver disease.

NCT ID: NCT02280551 Active, not recruiting - Alcohol Abuse Clinical Trials

The Australian Parental Supply of Alcohol Longitudinal Study (APSALS)

APSALS
Start date: March 2010
Phase:
Study type: Observational

Parents can positively influence their children's alcohol use. One strategy they use is to provide their children with alcohol, believing it is the best way to teach their children how to drink responsibly. The impact of parental supply is not well understood and may be unintentionally harmful. This study will research the consequences of parental supply within the broader context of parent, child and peer relationships. It will help to determine how parental supply influences the different patterns of adolescent alcohol consumption over time, providing essential information to help parents prevent alcohol misuse in their children. Parents can play a pivotal role in prevention of alcohol misuse, but at present we don't know exactly how.

NCT ID: NCT01678196 Active, not recruiting - PTSD Clinical Trials

Helping Families Help Veterans With PTSD and Alcohol Abuse: An RCT of VA-CRAFT

Start date: May 2013
Phase: N/A
Study type: Interventional

This project begins to evaluate the effectiveness of a web-based family outreach tool that is designed to promote treatment engagement among Veterans with posttraumatic stress disorder (PTSD) or alcohol use disorders (AUDs) but who have not yet engaged in mental health care. The National Center for PTSD has developed an on-line, Veteran-tailored, interactive web tool called VA - Community Reinforcement and Family Training (VA-CRAFT) that trains family members to effectively help their Veterans to engage in treatment for PTSD and/or AUDs. This project will provide preliminary information about VA-CRAFT's effectiveness.

NCT ID: NCT01663337 Active, not recruiting - PTSD Clinical Trials

Sequence of Symptom Change During AUD or PTSD Treatment for Comorbid PTSD/AUD

Start date: March 2013
Phase: N/A
Study type: Interventional

The broad, long-term objective of the current research is to improve treatment outcomes for individuals with comorbid posttraumatic stress disorder (PTSD) and alcohol abuse and dependence (AUD). The purpose of which is to evaluate changes in both PTSD symptoms and alcohol use and cravings associated with Cognitive Processing Therapy (CPT) or Relapse Prevention (RP) treatment in individuals with PTSD/AUD, along with mediators and moderators of outcomes. The study will randomize 235 PTSD/AUD participants recruited from the VA and from the community to CPT, RP, or Interactive Voice Response (IVR) assessment only (AO). Those in the AO condition will be re-randomized after the treatment phase to either RP or CPT. Individuals will be assessed pretreatment, immediately post-treatment, 3-, 6-, 9-, and 12-months post-treatment and will monitor symptoms daily throughout treatment.

NCT ID: NCT01621711 Active, not recruiting - Substance Abuse Clinical Trials

Continuing Care Following Drug Abuse Treatment: Linkage With Primary Care

Linkage
Start date: March 2011
Phase: N/A
Study type: Interventional

This component of a larger Center of Research Excellence Grant improves treatment for drug abuse by developing effective linkages between specialty drug treatment and primary health care.

NCT ID: NCT01567943 Active, not recruiting - Schizophrenia Clinical Trials

Contingency Management of Alcohol Abuse in the Severely Mentally ILL

CM ETG
Start date: March 2012
Phase: N/A
Study type: Interventional

The investigators will evaluate the efficacy of a comprehensive 12-week contingency management intervention for treating alcohol dependence for persons with severe mental illness who are seen within the context of a community mental health center setting. The primary contingency will be submission of alcohol-free urines. Additional reinforcers will be provided for intensive outpatient addiction treatment attendance. Reinforcers will be vouchers or actual items useful for day-to-day living. Participants will be 120 adults diagnosed with alcohol dependance and severe mental illness.

NCT ID: NCT01539525 Active, not recruiting - Clinical trials for Substance-Related Disorders

Screening to Augment Referral to Treatment- Project START

ProjectSTART
Start date: September 2010
Phase: Phase 2
Study type: Interventional

The investigators propose to use obstetric-gynecological clinics to conduct a randomized clinical trial that would compare two SBIRTS (Screening, Brief Intervention, Referral and Treatment), delivered either by a trained nurse or by computer, to usual care (a control condition). As part of this trial, the investigators will include outcomes that allow us to assess the cost effectiveness of these three conditions.