Testing a Smartphone App to Help Manage Craving and Reduce Substance or Behavioral Addictions in Adults
Led by Centre Hospitalier Charles Perrens, Bordeaux · Updated on 2025-08-14
274
Participants Needed
1
Research Sites
30 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness of a smartphone application designed to help people with substance use and behavioral addictions manage cravings and individual triggers for addictive behavior. This project builds on research from the University of Bordeaux, focusing on personalized intervention to reduce or stop substance use and addictive behaviors. The app is intended for people with various types of addictions and also assesses the risk of addiction transfers by monitoring concurrent substance use and behaviors.
Participants are randomly assigned to one of two groups. One group uses the full version of the smartphone app for four weeks, which combines Ecological Momentary Assessment EMA with Ecological Momentary Intervention EMI to target cravings and risky personal situations. The other group uses a restricted version of the app for four weeks, which only includes EMA through four daily electronic questionnaires evaluating their main problematic substance use or addictive behavior.
During the study, participants will be monitored for changes in their main addictive behavior over four weeks. Researchers will also assess addiction severity, craving levels, and usage patterns using questionnaires and daily app responses. Follow-up evaluations will happen at one and four months to measure the apps impact, feasibility, and acceptability. The total participation includes the four-week app usage period plus follow-up assessments, with safety monitored throughout the study.
CONDITIONS
Brief Title
Efficacy of a Smartphone App. Designed to Manage Craving & Individual Predictors of Substance Use/Addictive Behavior
Research Team
M
MARC AURIACOMBE, MD, Prof
A
AURELIEN VAUTARD
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Participants requesting help for substance or behavioral addiction in one of the participating specialized addiction treatment centers, with more than 1-month delay before treatment admission
Age 18 years or older
Diagnosed with at least one substance or behavioral addiction according to DSM-5 criteria
Affiliated with or beneficiary of a social security scheme
Provided free, informed, and written consent to participate
You will not qualify if you...
Medical, psychiatric, or addiction condition requiring immediate treatment intervention
Somatic, cognitive, or other disorders preventing use of the smartphone app (such as deafness, impaired vision, or illiteracy)
Difficulty understanding or writing in French
Not familiar with smartphone use
Currently participating in another study with an ongoing exclusion period
Deprived of liberty due to an ongoing legal procedure
Under legal protection, guardianship, or curatorship
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote) for eligibility assessment and consent
Treatment
Duration - 4 weeks
Participants use the smartphone application for 4 weeks to manage craving and individual predictors of substance use or addictive behavior. The experimental group uses the full app combining assessments and interventions, while the control group uses a restricted version for assessments only.
Daily electronic questionnaire responses via smartphone app
Follow-up
Duration - Up to 4 months after treatment
Participants are followed up to assess addiction severity, craving, app acceptability, feasibility, and impact on subsequent treatment.
Visits or assessments at 1 month and 4 months after treatment completion
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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Published Research Related To This Trial
The Craving-Manager smartphone app designed to diagnose substance use/addictive disorders, and manage craving and individual predictors of relapse: a study protocol for a multicenter randomized controlled trial.