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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02881424
Other study ID # 2014_51
Secondary ID 2014-A01761-46
Status Terminated
Phase
First received
Last updated
Start date March 2015
Est. completion date April 2018

Study information

Verified date October 2018
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background:

Alcohol-dependence is a chronic disease with a high risk of relapse. The main therapeutic outcome relies on relapse prevention which seeks to identify high risk situations and individual's response to these situations especially the emotional response to social environment. Alcohol-dependence also induces cognitive impairments leading to social cognition impairments increasing the risk of relapse.

Familiarity is a key process in social interactions: it induces the feeling of prior knowledge of a stimulus without remembering consciously its identity. Followed by a second process based on the contribution of contextual information (recollection) familiarity allows face recognition.

Main aim:

Study of familiarity for faces in alcohol-dependence

Secondary objectives:

Highlighting correlations between familiarity impairments and clinical outcomes


Description:

Familiarity will be tested by a specific familiarity task using an original paradigm. This paradigm allows the analysis of familiarity as a quantitative process as well as the analysis of personal familiarity to each subject. Three familiar and three unfamiliar faces are morphed in pairs for each participant. The displayed stimuli for each pair of faces are ten morphs with 5 to 95% of familiar face increasing by 10%. Participants are asked to press a button if the displayed stimulus seems familiar. At the end of the task each participant is asked to name the identity of the familiar faces (true or false recognitions, true or false omissions).

Each participant will undergo 2 visits.

- First visit:

- Checking the inclusion and non-inclusion criteria

- Clinical report and alcohol consumption evaluation

- Standardized psychiatric interview (Mini International Neuropsychiatric Interview - MINI)

- Neuropsychological tests (Montreal Cognitive Assessment - MoCA, "Batterie Rapide d'Efficience Frontale" - BREF, "Rappel Libre et Rappel Indicé à 16 items" - Grober & Buschke 's test - RL/RI 16)

- Second visit:

- Checking the non-consumption of alcohol and other drugs (cannabis, amphetamine, cocaine, methamphetamine, ecstasy, opioid)

- Task of familiarity with a controlling task

- Social cognition test (Movie for the Assessment of Social Cognition - MASC)


Recruitment information / eligibility

Status Terminated
Enrollment 42
Est. completion date April 2018
Est. primary completion date April 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- For all participants:

- With normal vision with or without glasses

- Understanding the Note of information and signing the consent form

- For alcohol-dependent patients:

- Being diagnosed with severe alcohol addiction (according to DSM-5)

- Currently abstinent

- For control subjects:

- Exclusion of severe alcohol addiction's diagnosis (according to DSM-5)

- Without antecedent or current neurologic disease

- Without antecedent or current psychiatric disease

- Non-taking psychotropic drugs

Exclusion Criteria:

- For all participants:

- Pregnant or breast-feeding women

- Cognitive impairment detected by a MoCA score inferior to < 26/30

- Physically or mentally not able to pass the tests of the study

- Taking an unauthorized drug the month before entering the study (other psychotropic drugs than the ones used for withdrawal or alcohol related complications for patients and any psychotropic drug for control subject)

- Being diagnosed with a severe addiction other than to caffeine or tobacco (according to DSM-5)

- Criteria for a plausible fetal alcohol syndrome

- For alcohol-dependent patients:

- Being diagnosed with schizophrenia or bipolar disorder (according to DSM-5)

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France University Hospital, Lille - CSAPA Lille
France University Hospital, Lille - Fontan 2 Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Familiarity threshold calculated from the psychometric function of each participant 3 years
Secondary Alcohol consumption alcohol consumption evaluation 3 years
Secondary MocA score Score at the Montreal Cognitive Assessment 3 years
Secondary BREF score neuropsychological score 3 years
Secondary RL/RI score neuropsychological score 3 years
Secondary non-consumption of alcohol duration non-consumption of alcohol duration 3 years
Secondary social cognition test social cognition test score 3 years
Secondary concomitant treatment concomitant treatment posology 3 years
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