Can a brain scan and your phone predict where depression goes next?
NCT ID NCT07033923
First seen Sep 21, 2026 · Last updated Sep 21, 2026
Summary
Researchers want to know whether mathematical models of mood, combined with brain imaging and daily smartphone check-ins, can describe mood in a way that matters for depression and bipolar disorder. The study enrolls three groups of 96 people each: those with depression, those with bipolar disorder, and healthy volunteers. Participants complete a brain MRI session with optional cognitive tests, then rate their mood and daily events on a phone app over time. Two optional add-ons use the app to track emotions passively and to record voice for vocal and language analysis.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Brain MRI plus smartphone-based mood tracking and cognitive tests
- What this could lead to
- If the approach works, doctors might one day use a short brain scan plus daily phone check-ins to predict how someone's depression or bipolar disorder will change over the following months.
- What could go wrong
- This is an observational study, not a treatment, so it will not cure or ease mood disorders. The models may fail to predict real-life mood changes, and the findings may not apply to everyone with these conditions.
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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About 588 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2024
- Expected to finish
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Jul 2029
An estimate. End dates often move.
- 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 years and older
- 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: Common between groups (DD, BD, control and GP): * Having given informed and written consent * Being covered by social security For patients with depressive disorder (DD): * Having been diagnosed with characterized depressive episode (F32, F33, F34) according to the ICD-10, by a psychiatrist, or having presented this diagnosis during the past 12 months For patients with bipolar disorder (BD): * Presenting a diagnosis of bipolar mood disorder (F31) according to ICD-10, by a psychiatrist * Having presented a mood episode (F31.0 - F31.6) diagnosed during the past 12 months by a psychiatrist Exclusion Criteria: Common between groups (DD, BD, control and GP): * Inability to carry out daily monitoring on mobile application for 12 months * legal protection measure (guardianship or curatorship) For control group: * Current diagnosis of psychiatric disorder in ICD-10 (F20-F98) or prescription of psychotropic treatment * History of depression (F32) * Syndrome of dependence on a psychoactive substance other than tobacco * Neurological history (in particular history of stroke, coma, epilepsy, neuro- inflammatory, or neuro-degenerative disease) * Inability to carry out daily monitoring on mobile application for 12 months For patients and healthy volunteers for whom an MRI (without injection of contrast agent) is proposed * Contraindication to MRI: cardiac pacemaker not compatible with MRI, heart valve implant, implant or metallic foreign body * Pregnant woman (at the time of MRI)
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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- Groupe hospitalo-universitaire Paris Psychiatrie et Neurosciences
RECRUITINGParis, Paris, 75014, France
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Assistance Publique - Hôpitaux de Paris GH Pitié-Salpêtrière
RECRUITINGParis, 75651, France
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