ClinicalTrials.gg
Not yet recruitingNCT06981546MOGADORUpdated May 20, 2025

Modeling Clinical Outcomes in Gambling Addiction

An observational study in Gambling Disorder, sponsored by Hospices Civils de Lyon. Not yet recruiting at 9 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-05-20.

Sponsored by Hospices Civils de Lyon · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
268
Ages
18 Years and older
Sex
All
01

Study summary

Gambling disorder (GD) is recognized as an addictive disorder. Financial consequences of GD are often dramatic, inducing professional, familial, legal and medical repercussions and particularly mental health consequences.

MOGADOR is a longitudinal, multicentric, prospective, prognostic study, which aims to identify factors predicting the evolution of french patients with GD in care centers particularly involved in the management of GD. The main goal will focus on evolution of DSM-5 (Diagnostic and Statistical Manual of Mental Disorder 5th edition) GD criteria during the first year of follow-up. The prognostic factors will be collected at base-line and they will be considered to influence the long-term prognosis of patients.

For patients suffering of GD, our main hypothesis is that initial factors like individual socio-demographic characteristics, clinical psychiatric profiles, addiction comorbidities, and behaviour are associated with the clinical prognosis (total remission of DSM-5 criteria of GD at 12 months).

MOGADOR will be the first study, aiming to model prognostic aspects of GB in populations specially monitored for this disorder.

02

Conditions studied

  • Gambling Disorder

Browse trials for

Keywords

  • Gambling disorders
  • Modeling outcomes
  • Socio-demographic Characteristics
  • Clinical psychiatric profiles
03

In context

Gambling

158 studies on the registry are indexed under Gambling; 42 are open to participants now.

This study's planned enrollment of 268 is above the median of 213 across 23 observational studies indexed under Gambling.

Browse Gambling studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,866 studies on the registry; 448 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

268 patients with gambling disorder according to DSM-5 criteria newly managed in one of the participating centers or who had an interruption in management of more than 6 months.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patient, male or female, over 18 years old, consulting in one of the participating centers.
  • criteria for gambling disorder at inclusion: at least 4 criteria present in the 12 months preceding the study.
  • First treatment for gambling disorder or no treatment in the last 6 months (initiation or re-initiation of care).

Exclusion criteria

Exclusion Criteria:

  • Unable to be reached by phone.
  • Unable to use the internet.
  • Patient under antiparkinsonian treatment of the dopaminergic family.
  • Being treated with a drug that may trigger/increase symptoms of gambling disorder (e.g. dopamine agonist).
  • Subject under guardianship.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
268 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients with gambling disorder

    OGADOR will focus exclusively on patients with DSM-5 criteria for gambling disorder and on demand for medical care. In this study psychiatric and addictological comorbidities, frequent in such a cohort, will constitute a specific inclusion factor, key characteristic leading an analysis of the impact on the patient prognosis.

06

What researchers measure

Primary outcomes

  1. Partial remission of gambling disorder at 12 months (strictly less than 4 DSM-5 criteria)

    Assessment of DSM-5 criteria will be performed by the clinician, and by a previously trained CRA if clinical follow-up is discontinued.

    Time frame: DSM-5 criteria assessment will be conducted at 9 and 12 months after inclusion.

  2. modeling prognostic factors

    The prognostic factors, studied will be: number of initial DSM-5 criteria, gender, age, marital status, housing, employment status, socioeconomic level, time spent gambling, impulsivity, type of gambling, location of gambling, and also the factor with the strongest association in univariate analysis among the following factors: * Depression (PHQ scale), * Anxiety (GAD scale), * Quality of life (SF-36 scale).

    Time frame: at inclusion visit.

07

Study locations

9 sites
  • Hôpital Jen Minjoz, CHU de Besançon
    Besancon, 25030, France
  • Service Universitaire d'Addictologie de Lyon (SUAL), CH Le Vinatier
    Bron, 69500, France
  • Service Universitaire d'Addictologie de Lyon (SUAL), Groupement Hospitalier Est
    Bron, 69500, France
  • Service Universitaire d'Addictologie, CHU de Clermont-Ferrand
    Clermont-ferrand, 63000, France
  • Name of location * Service d'Addictologie, Groupe Hospitalier Seclin Carvin
    Lille, 59000, France
  • Centre Expert Régional du Jeu Pathologique (CERJeP Limousin)
    Limoges, 87000, France
  • Service Universitaire d'Addictologie, CHU de Nîmes
    Nimes, 30000, France
  • Assistance Publique des Hôpitaux de Paris, Hôpital Marmottan
    Paris, 75017, France
  • Hôpital de Bellevue, CHU de St-Etienne
    St-etienne, 42000, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 20, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06981546
Responsible party
Sponsor
First posted
May 20, 2025
Start date
Sep 1, 2025 (estimated)
Primary completion
Sep 1, 2029 (estimated)
Completion
Sep 1, 2030 (estimated)
Last update
May 20, 2025

Study contacts

Véronique FONTEILLE, MD, PhD
Contact
veronique.fonteille@chu-lyon.fr
04 72 11 80 64
Pauline DROUIN
Contact
pauline.drouin@chu-lyon.fr

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion