Role of Craving in the Transition Across Level of Addiction Severity: A Longitudinal Study.
CARDEMA
Symptom Networks Characteristics and Centrality of Craving as Markers of Transition Across Levels of Addiction Severity: A Longitudinal Study
2 other identifiers
observational
700
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2026
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 20, 2026
CompletedFirst Submitted
Initial submission to the registry
July 2, 2026
CompletedFirst Posted
Study publicly available on registry
July 29, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2031
July 29, 2026
July 1, 2026
4.5 years
July 2, 2026
July 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (8)
Craving centrality in the DSM-5 Substance Use Disorder diagnostic criteria network
Craving centrality will be quantified as the expected influence centrality of the DSM-5 craving criterion within a cross-sectional network including the 11 DSM-5 Substance Use Disorder diagnostic criteria. Expected influence values will be estimated for each assessment (baseline, 1-year and 2-year follow-up) and compared across addiction severity groups and severity transition groups.
Baseline, 1-year follow-up, 2-year follow-up
Global connectivity of the DSM-5 Substance Use Disorder diagnostic criteria network
Global network connectivity will be quantified as global strength (sum of absolute edge weights) of the DSM-5 diagnostic criteria network. Global strength estimates will be compared across addiction severity groups and severity transition groups.
Baseline, 1-year follow-up, 2-year follow-up
Predictability of nodes in the DSM-5 Substance Use Disorder diagnostic criteria network
Node predictability will be calculated as the proportion of variance explained (R²) for each DSM-5 diagnostic criterion by its neighboring nodes within the network. Mean node predictability will be reported and compared across addiction severity groups and severity transition groups.
Baseline, 1-year follow-up, 2-year follow-up
Differences in DSM-5 Substance Use Disorder diagnostic criteria network structure
Differences in overall network structure and global strength between addiction severity groups and severity transition groups will be evaluated using the Network Comparison Test (NCT). The reported outcome will be the statistical significance of differences in network structure.
Baseline, 1-year follow-up, 2-year follow-up
Temporal network structure of ecological momentary assessment (EMA) symptoms
Temporal directed network parameters estimated from ecological momentary assessment data including primary substance use, craving, affect, self-efficacy, withdrawal symptoms, cues, stress, coping, sleep, impulsivity and other daily-life variables. Temporal edge weights will be estimated using multilevel vector autoregressive models and compared across severity groups and severity transition groups.
Baseline, 1-year follow-up, 2-year follow-up
Contemporaneous network structure of ecological momentary assessment (EMA) symptoms
Contemporaneous partial correlation network estimated from ecological momentary assessment variables. Network structure will be compared across severity groups and severity transition groups.
Baseline, 1-year follow-up, 2-year follow-up
Between-subject network structure of ecological momentary assessment (EMA) symptoms
Between-subject partial correlation network estimated from ecological momentary assessment variables. Network structure will be compared across severity groups and severity transition groups.
Baseline, 1-year follow-up, 2-year follow-up
Individual network invariance assessed by the Individual Network Invariance Test (INIT)
Individual Network Invariance Test (INIT) results will assess whether each participant's symptom network significantly differs from the group-level network. The proportion of significant INIT tests will be reported and compared across severity groups.
Baseline, 1-year follow-up, 2-year follow-up
Study Arms (5)
Alcohol
Participants with various level of Alcohol Use Disorder severity
Tobacco
Participants with various level of Tobacco Use Disorder severity
Cannabis
Participants with various level of CannabisUse Disorder severity
Opiates
Participants with various level of Opiates Use Disorder severity.
Stimulants
Participants with various level of Stimulant Use Disorder severity
Interventions
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.
Eligibility Criteria
Patients who have initiated treatment for addiction in a Centre de Soin et d'Accompagnement et de Prévention en Addictologie in France; People with addiction recruited from the general population via recruitment campaigns (posters, partner institutions websites, newspaper, social media); Users of Kanopée, a smartphone application developed by SANPSY Lab, who reported problematic tobacco, alcohol or cannabis use.
You may qualify if:
- 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.
You may not qualify if:
- 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.
- Be deprived of liberty due to an ongoing legal procedure.
- Be under legal protection.
- Be under guardianship or conservatorship.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Bordeauxlead
- Hospices Civils de Lyoncollaborator
Study Sites (1)
Université de Bordeaux CNRS UMR 6033 SANPSY
Bordeaux, 33000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Fuschia SERRE
University of Bordeaux
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 2, 2026
First Posted
July 29, 2026
Study Start
May 20, 2026
Primary Completion (Estimated)
December 1, 2030
Study Completion (Estimated)
June 1, 2031
Last Updated
July 29, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will share
Deidentified individual participant data will be available upon reasonable request to the principal investigator. Access will be granted to researchers who provide a methodologically sound proposal for achieving the aims of the approved proposal. A data access agreement may be required before the data are released.