Can brain scans cure depression? new study tests memory training
NCT ID NCT03428828
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested a new way to help people with depression that hasn't improved with standard treatments. 60 adults learned to increase activity in a brain area linked to positive memories using real-time feedback from an MRI machine. The goal was to see if this training could reduce depression symptoms.
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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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60 people
The number who actually took part.
- Started
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Oct 2018
- Finished
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Mar 2026
- 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 55 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * right-handed adults (ages 18 - 55) with a primary diagnosis of MDD according to diagnostic criteria DSM-5 for recurrent MDD who are currently depressed will be recruited to participate * must be able to give written informed consent prior to participation * must have fewer than 45% memories categorized as specific on the Autobiographical Memory Test * must have a SHAPS score \> 4, indicating the presence of anhedonia * unmedicated or stable on an SSRI antidepressant regime (at least 3 weeks to ensure symptoms are stable) * previously failed to respond to two previous SSRI medications according to either a medical record review or clinical interview during Visit 1 Exclusion Criteria: * have a clinically significant or unstable cardiovascular, pulmonary, endocrine, neurological, gastrointestinal illness or unstable medical disorder * met DSM-IV criteria for alcohol and/or substance dependence (other than nicotine) within 12 months prior to screening * have a history of traumatic brain injury * are unable to complete MRI scan due to claustrophobia or general MRI exclusions (e.g., shrapnel inside body) * are currently pregnant or breast feeding * are unable to complete questionnaires written in English * current (within 3 weeks of testing) use of any antipsychotics, anticonvulsants, stimulants, benzodiazepines, beta-blockers, or other medications (except SSRI antidepressants) likely to influence cerebral blood flow. Effective medications will not be discontinued for the purposes of the study. Inclusion of patients on stable antidepressant medications was decided in order to allow generalization towards a real world population * have a DSM-5 diagnosis of psychotic or organic mental disorder, bipolar I or II disorder or any past or current manic or hypomanic symptoms, autism, or a primary diagnosis of an anxiety disorder (though co-morbid anxiety will not be excluded) * have any eye problems or difficulties in corrected vision.
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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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University of Pittsburgh
Pittsburgh, Pennsylvania, 15261, United States
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Other studies related to the condition(s) this trial covers.
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