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Evaluative Conditioning: A Brief Cognitive Intervention Aimed to Modify Addiction Behaviour of Alcohol-dependent Patients (CEAlcool)

C

Centre Hospitalier Henri Laborit

Status

Withdrawn

Conditions

Cognitive Intervention to Modify Addiction Behaviour of Alcohol-dependent Patients

Treatments

Other: Evaluative Conditionning Task

Study type

Interventional

Funder types

Other

Identifiers

NCT05341934
2017-A02120-53

Details and patient eligibility

About

Evaluative Conditioning: A Brief Cognitive Intervention Aimed to Modify Addiction Behaviour of Alcohol-dependent Patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants in this study will be patients:
  • With an alcohol use disorder according to DSM 5
  • Follow-up at the Laborit Hospital Center
  • Aged between 18 and 70 years with informed consent after receiving written information
  • Engaged in a process to reduce alcohol consumption
  • With a score of MOCA> 20
  • Whose mother tongue is French
  • Patients benefiting from social security or benefiting from it through a third party in accordance with the french law on research involving the human person.

Exclusion criteria

    • Patient with less than 6 Heavy Drinking Days in the month
  • Patient with Schizophrenia
  • Patient with bipolar disorder Type 1
  • Patient with Korsakoff syndrome or degenerative neurological disorder
  • Patient with hearing impairment, uncorrected visual impairment
  • Patient under curatorship or guardianship
  • Patient with addiction to another substance other than tobacco
  • Patient already enrolled in another interventional study
  • Pregnant or nursing woman
  • Patient with difficulties of expression or comprehension in French
  • Patients in emergency situations or unable to give their consent.

Output Criteria:

  • Patient who has manifested verbally or in writing, the desire to leave the study in progress.
  • Patient who will be hospitalized during the study for a problem related to his addiction.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups, including a placebo group

Conditionning
Active Comparator group
Treatment:
Other: Evaluative Conditionning Task
Placebo
Placebo Comparator group
Treatment:
Other: Evaluative Conditionning Task

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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