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Impact of a Self-Exclusion Procedure Optimized by an Extension of the Suspension of Commercial Solicitations — PASS  

Gambling Disorder Clinical Trial

Official title:
Impact of a Self-Exclusion Procedure Optimized by an Extension of the Suspension of Commercial Solicitations

Clinical Trial Summary

Considering that self-exclusion from gambling on a particular website is an intervention for and by individuals who have developed a gambling disorder, it is currently exclusively a behavioural intervention in the sense that it prevents the behaviour Resumption of commercial solicitations only in the period when gambling is not accessible in the corresponding website , through voluntary self-exclusion (where the gambler prevents himself or herself from gambling), does not appear to be sufficient to prevent relapse. Early commercial solicitations, in the immediate intercourse after the end of the self-exlcusion period may precipitate relapse in gamblers whose behaviour change is by definition recent, and who have only received a behavioural measure. The investigators hypothesize an improved efficacy as measured by reduced gambling after a self-exclusion optimized by a period of suspension of commercial solicitations extended to 9 months, compared to self-exclusion with the standard procedure. Gamblers will be randomized according to an a priori randomization list.

Clinical Trial Description

This is a study evaluating the impact of PMU's implementation of an optimized self-exclusion procedure by extending the suspension of commercial solicitations for a total of 9 months, the self-exclusion being referred to as a non-medical "responsible gambling" tool, compared to the standard procedure. The self-excluded gamblers will be randomized according to an a priori randomization list, and will receive either the optimized self-exclusion procedure A or the standard self-exclusion procedure B. The study consists of a comparison between two groups A and B. The study involves non-medical gambling and socio-demographic data, routinely recorded in a regulatory manner with a permanent CNIL authorization PMU. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05413564
Study type Interventional
Source Centre Hospitalier Universitaire de Nimes
Contact Amandine LUQUIENS, MD, PhD
Phone 0609566346
Email amandine.luquiens@chu-nimes.fr
Status Recruiting
Phase N/A
Start date May 30, 2022
Completion date May 31, 2025
View Details
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