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Clinical Trials in France / NCT07734363
Recruiting Observational

Role of Craving in the Transition Across Level of Addiction Severity: A Longitudinal Study.

NCT07734363 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-05-20
Last updated
2026-07-29

Condition(s) studied

Addiction

Investigational drug(s) / intervention(s)

Observational assessments (EMA and annual DSM-5 evaluations)

Observational assessments (EMA and annual DSM-5 evaluations): Participants are observed over two years. Annual DSM-5 diagnostic criteria for substance use disorders (SUD) are assessed, and participants complete 2-week EMA protocols measuring substance use, craving, and related factors four times per day. No intervention is administered.

Study summary

Substance/Alcohol Use disorders are defined as a loss of control over the use despite harmul consequences, as well as an intense and persistent urge to use, also called craving. Previous research has shown that craving is central among the diagnostic criteria for addiction, suggesting that it may be important in the onset and persistence of addiction.

Addiction develops progressively, and it appears crucial to identify predictive markers of the transition from one level of severity to another over time. One hypothesis is that more closely linked symptoms (meaning symptoms that influence each other more) could be associated with greater severity and/or with the evolution of addiction severity over time.

The aim of this project is to explore how the characteristics of the association between addiction symptoms (diagnostic criteria and symptoms as they occur in daily life), and the importance of craving relative to other symptoms, could serve as markers of different addiction severities and of the transition across these levels of severity.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria * Be over 18 years of age * Identify a primary substance as a main problematic substance use. * Be a regular user (at least twice a week in the last 30 days) of a primary substance (defined as their main problematic substance use). * Present a current diagnosis of SUD for this primary substance according to DSM-5 criteria. Exclusion Criteria * Medical, psychiatric or addiction condition that warrants immediate inpatient treatment intervention. * Somatic, cognitive or other disorders preventing the use of the smartphone device (deafness, impaired vision, illiteracy….). * Not being familiar with the use of smartphone * Having a smartphone not compatible with the application and being unable to visit the laboratory to receive a loaner phone for the study. * Difficulty in understanding and/or writing and/or reading French. * Individuals participating in another study that includes an ongoing exclusion period. * Be deprived of liberty due to an ongoing legal procedure. * Be under legal protection. * Be under guardianship or conservatorship.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Université de Bordeaux CNRS UMR 6033 SANPSY Bordeaux France Recruiting

More University of Bordeaux trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07734363 on ClinicalTrials.gov ↗ ← All trials in France