ClinicalTrials.gg
RecruitingNCT07421765PRAT-JEUUpdated Feb 19, 2026

Interaction Between Atypical Work Schedules and/or Idel Time at Work on At-risk Gambling Practices

An observational study in Gambling, Shift Work and Addictive Behavior, sponsored by Centre Hospitalier Universitaire de Nīmes. Recruiting at 2 sites in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-19.

Sponsored by Centre Hospitalier Universitaire de Nīmes · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
25
Ages
18 Years and older
Sex
All
01

Study summary

At-risk gambling causes individual and social harm, influenced by environmental, psychological, and socioeconomic factors. In France, 5% of adult gamblers show at-risk gambling practices. Atypical work schedules and idle time at work could increase this risk, but few studies have explored this. These working conditions impact the mental and cognitive health of workers, potentially contributing to at-risk gambling, especially during periods of idle time The study authors wish to explore the links between atypical work schedules, idle time at work, and at-risk gambling practices, considering social norms and individual vulnerabilities.

02

Conditions studied

  • Gambling
  • Shift Work
  • Addictive Behavior
  • Boredom
  • Impulsivity
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 25 is below the median of 213 across 23 observational studies indexed under Gambling.

Browse Gambling studies →

Lead sponsor

Centre Hospitalier Universitaire de Nīmes is the lead sponsor of 595 studies on the registry; 90 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

Patients will be screened on an ongoing basis from the active caseload of the addiction services at the University Hospitals of Nantes and Nîmes, and information about the study will be disseminated on social media.

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

  • Living with current or remission gambling, as assessed using the Problem Gambling Index Scale (PGSI) score of ≥5
  • Having been employed during the current year
  • Patients with a personal mobile phone number and email address who agree to share them for research

Exclusion criteria

Exclusion Criteria:

  • Patient in an exclusion period determined by another study
  • Patient who has expressed their opposition to participating in this research
05

Study design

Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
25 participants (estimated)
Patient registry
No

Groups and cohorts

  • People with gambling disorder

    Other: semi-structured interview

Interventions

  • Othersemi-structured interview

    After having completed a consent form and online self-questionnaires, participants will take part in online interviews lasting 45 to 60 minutes

06

What researchers measure

Primary outcomes

  1. Identify the predominant lexical classes in participants' discourse

    Hierarchical descending classification illustrated by a dendrogram

    Time frame: Day 0

  2. Describe the predominant lexical classes in participants' discourse

    Description of lexical classes and forms associated with the classes

    Time frame: Day 0

Secondary outcomes

  1. Identify links between work organization, environment and personal working time during atypical working hours

    Forms associated with atypical working hours

    Time frame: Day 0

  2. To identify links between work organization, environment and personal working time during periods of inactivity at work

    Forms associated with periods of inactivity at work

    Time frame: Day 0

Other outcomes

  1. Atypical working hours pattern

    If yes, type of atypical work schedule

    Time frame: Day 0

  2. Amount of inactivity time at work

    Cumulative duration for the past 5 days (minutes)

    Time frame: Day 0

  3. Proportion of gambling practices

    From exclusively in-person to exclusively online

    Time frame: Day 0

  4. At-risk gambling

    Assessed using the French version of the Problem Gambling Index Scale (PGSI) scale using cut-off ≥5

    Time frame: Day 0

  5. Perceived prevalence of betting by colleagues

    Measured on custom tool combining items from two existing questionnaires: Gambling Quantity and Perceived Norms Scale (GQPNS); Gambling Attitudes and Injunctive Norms Scale (GAINS)

    Time frame: Day 0

07

Study locations

1 of 2 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Feb 2026; primary completion for Feb 2027, 12 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 9, 2026
First posted
Feb 19, 2026
StartEst.
Feb 5, 2026
Primary completionEst.
Feb 2027
CompletionEst.
Feb 2027
Last update
Feb 19, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 19, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07421765
Responsible party
Sponsor
First posted
Feb 19, 2026
Start date
Feb 5, 2026 (estimated)
Primary completion
Feb 2027 (estimated)
Completion
Feb 2027 (estimated)
Last update
Feb 19, 2026

Study contacts

Amandine Luquiens
Contact
amandine.luquiens@chu-nimes.fr
04.66.68.69.98
Amandine Luquiens
principal investigator · Centre Hospitalier Universitaire de Nīmes

Oversight

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

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