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Alcoholism clinical trials

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NCT ID: NCT03810924 Completed - Clinical trials for Alcohol Use Disorder

Stress-related Predictor Profiles in Human Addiction

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

Long-term aim is the definition of a setup of mobile sensors and their integration in a mobile infrastructure that allows the prediction of stress related alcohol intake in an ambulatory setting. Here, we aim to identify stress- and alcohol cue-related physiological markers in a lab experiment to assess interactions between acute psychological vs. physical stress exposure and alcohol cue-exposure regarding their effects on measures relevant for the development and maintenance of Alcohol Use Disorder (AUD). Further, we aim to identify neural correlates in brain circuits of motivational, cognitive, and affective processing. In addition to applying established stress-related markers, we will integrate innovative sensor-based measures.

NCT ID: NCT03809286 Recruiting - Clinical trials for Alcohol Use Disorder

The Effect of rTMS to the Prefrontal Cortex in Alcohol Use Disorder

MAGNA
Start date: June 24, 2019
Phase: N/A
Study type: Interventional

The goal of this study is to investigate a treatment approach for alcohol use disorder (AUD) using a novel form of brain stimulation called deep repetitive transcranial magnetic stimulation (rTMS). The investigators will be targeting frontal regions of the brain that are important for memory and decision making. These brain regions have been shown to be impaired in patients with AUD. Previous studies have mostly used rTMS to a different frontal brain region that is not as deep. These studies have shown that rTMS can reduce craving for alcohol, but there is a lack of research showing that rTMS impacts alcohol consumption.

NCT ID: NCT03807544 Completed - Clinical trials for Alcohol Use Disorder

Treatment Parameters for the Empower Neuromodulation System (ENS)

AUD1
Start date: January 15, 2019
Phase: N/A
Study type: Interventional

The subject will be administered a treatment at a treatment location and then be asked if he/she believes it is the active treatment, sham treatment, or does not know. A clinical-grade nerve conduction assessment system will be used both to provide electrical stimulation at four locations to record peripheral responses. The subject will self-administer two treatment sessions at two active treatment sites.

NCT ID: NCT03806491 Completed - Insomnia Clinical Trials

CBT-I on Alcohol Treatment Outcomes Among Veterans

Project SAVE
Start date: July 15, 2019
Phase: N/A
Study type: Interventional

Project SAVE aims to examine the feasibility, acceptability, and initial efficacy of a CBT-I supplement to alcohol treatment of Veterans.

NCT ID: NCT03803709 Recruiting - Alcoholism Clinical Trials

Dietary Fiber Intake in Alcohol-dependent Patients

Start date: July 4, 2017
Phase: N/A
Study type: Interventional

The alcohol problem affects 7.5% of the population in Europe and represents a major public health problem. Alcoholism is also a major cause of undernutrition. Diet is a major factor influencing the composition of the intestinal microbiota and previous studies, carried out at Saint-Luc clinics and catholic university of Louvain, show that alcoholic patients suffer from dysbiosis, that is a significant alteration of the gut microbiota. The investigator's preliminary studies, carried out at the Integrated Unit of Hepatology of Saint-Luc Clinics, have shown that alcohol represents more than 40% of total caloric intake in alcohol-dependent patients. In addition, alcoholic patients have an insufficient intake of dietary fiber, that is to say a contribution lower than the Belgian nutritional recommendations. Indeed, the Conseil Supérieur de la Santé recommends a total amount of dietary fiber equal to or greater than 25 grams per day to ensure correct intestinal function. Fructan-type dietary fiber (inulin and fructo-oligosaccharides) is found naturally in many fruits and vegetables (Jerusalem artichokes, asparagus, artichokes, onions, garlic, chicory roots, bananas). They are neither absorbed nor digested by human enzymes but fermented selectively by intestinal bacteria. A good digestive tolerance to dietary fiber supplementation has been observed in healthy subjects as well as in obese patients, in previous studies conducted at catholic university of Louvain and Saint-Luc clinics. However, a nutritional rebalance via fiber supplementation and digestive fiber tolerance have never been tested in an alcohol-dependent population. The primary objectives of this academic research project in nutrition, carried out in alcohol-dependent patients, are as follows: 1. restore a nutritional balance as recommended by the Conseil Supérieur de la Santé via a dietary fiber intake 2. to study digestive tolerance to fibers 3. to study the intestinal and psychological well-being related to a fiber intake Depending on the results obtained during the achievement of the primary objectives, the biological samples (blood, stool) collected during the study will be used to analyze the composition of the intestinal microbiota and the plasma markers associated with intestinal function.

NCT ID: NCT03786276 Completed - Clinical trials for Alcohol Use Disorder

Virtual Reality- Working Memory Retraining

VR-WMR
Start date: February 1, 2019
Phase: N/A
Study type: Interventional

This study will establish the acceptability and feasibility of enrolling and retaining heavy drinking Veterans with mild traumatic brain injury (mTBI) in an 8-week, randomized cross-over design trial of active VR working memory retraining (WMR). This study will also seek to establish the efficacy of active VR-WMR to increase performance in executive function.

NCT ID: NCT03765476 Active, not recruiting - Clinical trials for Alcohol Use Disorder

Validation of a Training Program for Patients With Alcohol Use Disorder

Start date: July 1, 2018
Phase: N/A
Study type: Interventional

This study aims to detect how the Web-based program SALIENCE affects patients with alcohol-use Disorder in terms of craving, cognitive functions and risk of relapse.

NCT ID: NCT03764098 Recruiting - Alcohol Use Clinical Trials

Mechanistic Evaluation of Guanfacine on Drinking Behavior in Women and Men With Alcohol Use Disorders

Start date: August 10, 2020
Phase: Phase 2
Study type: Interventional

For this protocol, the investigators plan to collect pilot data to examine sex differences in guanfacine's effect on 1) counteracting stress and stimulation based drinking behavior in the laboratory and 2) improving clinical outcomes during a subsequent treatment phase.

NCT ID: NCT03758274 Completed - Clinical trials for Alcohol Use Disorder

Talk Therapy by Phone to Promote Treatment for Alcohol Problems

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

A small percentage of individuals with alcohol use disorder (AUD) obtain alcohol-related care despite research showing that treatment is effective. This randomized controlled trial tests the efficacy of a brief, phone based cognitive behavioral intervention to increase treatment engagement, improve alcohol related outcomes, and show that treatment engagement is a mechanism for the improved outcomes in individuals with AUD.

NCT ID: NCT03758053 Active, not recruiting - Clinical trials for Alcohol Use Disorder

Adverse Childhood Experiences in Substance-related Disorders

Start date: December 15, 2018
Phase:
Study type: Observational

Aversive childhood experiences (ACE) and their relation to the development of an alcohol use disorder will be measured with fMRI.