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Clinical Trial Summary

The individual and societal cost of alcohol use disorders (TUAL), present in 10% of the population in France, is considerable. Despite psychotherapeutic and drug addiction treatment, the relapse rate remains very high, partly because of their very frequent cognitive disorders. In fact, more than 75% of TUAL patients present to varying degrees neuropsychological alterations that are only rarely detected and never treated. However, these cognitive disorders limit the benefit of psychotherapeutic care, reduce compliance with pharmacological treatments and hinder the patient's ability to change his behavior with respect to alcohol. An innovative way to promote the maintenance of the therapeutic contract, and therefore to reduce alcohol consumption in these patients, would be to improve their cognitive functioning. The objective of this study is to measure the efficacy of a non-drug treatment, based on a specific and personalized cognitive remediation program, compared to a standard treatment in Day Hospitalization, in order to reduce the rate of relapse very high in TUAL. It is a randomized, single-blind study with two parallel groups of patients with post-weaning neuropsychological disorders: REMED (cognitive remediation) and CONTROL (usual care).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03335215
Study type Interventional
Source University Hospital, Caen
Contact
Status Not yet recruiting
Phase N/A
Start date February 1, 2018
Completion date February 1, 2020

See also
  Status Clinical Trial Phase
Completed NCT04502589 - Open Label Pilot Study of Perampanel for the Treatment of Alcohol Use Disorder Phase 1/Phase 2
Completed NCT02030288 - Relational Agent for Alcohol Screening and Treatment N/A