Scientists use brain scans and phones to decode addiction
NCT ID NCT02334956
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study combined brain imaging with real-world data from mobile devices to explore how addiction affects the brain. Researchers scanned the brains of 107 people with alcohol, cannabis, or nicotine dependence, along with healthy controls. They also tracked cravings and daily functioning using mobile technology. The goal was to better understand the brain processes behind addiction, not to test a new treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help researchers better understand how addiction works in the brain, potentially pointing toward new ways to predict or manage cravings.
- What could go wrong
- This is an observational study, not a treatment trial. It is small and early-stage, so findings may not apply to everyone or lead directly to new therapies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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107 people
The number who actually took part.
- Started
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Mar 2015
- Finished
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Jan 2018
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 64 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Inclusion criteria patient: * Aged 18-64 years * Being affiliated to health insurance * Having signed an informed consent (later than the day of inclusion and before any examination required by research) * Participation in the study MOBICOG for patients with addiction * Fulfils diagnostic criteria for one of the following groups: Group A: Patients with current (last 12 months) Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) substance addiction (Alcohol / Cannabis / Nicotine); initiation of treatment for addiction within 30 days preceding enrollment in the study; absence of other axis 1 psychiatric disorder currently being treated (by psychotherapy or pharmacotherapy); absence of current or lifetime bipolar disorder or schizophrenia. Group AM: Patients with current (last 12 months) DSM-IV substance addiction (Alcohol / Cannabis / Nicotine); initiation of treatment for addiction within 30 days preceding enrollment in the study; presence of currently treated unipolar mood disorder (by psychotherapy or pharmacotherapy); absence of current or lifetime bipolar disorder or schizophrenia. Group AS: Patients currently treated for DSM-IV schizophrenia (last 12 months) with DSM-IV substance addiction (Alcohol / Cannabis / Nicotine); absence of other axis 1 psychiatric disorder currently being treated (by psychotherapy or pharmacotherapy); absence of current or lifetime bipolar disorder. Inclusion criteria healthy volunteers: * Aged 18-64 years * Participation in the study MOBICOG * Being affiliated to health insurance * Having signed an informed consent (later than the day of inclusion and before any examination required by research) * Healthy volunteers without current addiction and with no other currently-treated axis 1 DSM-IV disorder (by psychotherapy or pharmacotherapy); absence of current or lifetime bipolar disorder or schizophrenia Exclusion Criteria: * Presence of a counter-indication for MRI * Presence of any health problem preventing travel to the imaging service of the University Hospital * Being unable to provide consent to participate * Pregnant or breastfeeding woman
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU de Bordeaux
Bordeaux, 33000, France
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Hôpital Charles Perrens
Bordeaux, 33076, France
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