Shocking news: brain zaps may ward off dementia
NCT ID NCT02386670
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This 7-year study tests whether a combination of mild electrical brain stimulation (tDCS) and computer-based memory exercises can slow mental decline and prevent Alzheimer's dementia. It involves 375 older adults with mild cognitive impairment or depression (both risk factors for Alzheimer's). Participants receive either real or sham (placebo) stimulation plus real or sham cognitive training, and their thinking skills are tracked over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial direct current stimulation (tDCS) and cognitive remediation
- What this could lead to
- If it works, this could point toward a non-drug way to slow memory loss and prevent Alzheimer's in high-risk older adults.
- What could go wrong
- This is a mid-stage trial, and the intervention is complex—results may not show clear benefit, or the effect may be too small to matter. The sham control helps, but real-world use is uncertain.
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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375 people
The number who actually took part.
- Started
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Jan 2015
- Expected to finish
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Dec 2026
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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60 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.
MCI Group Inclusion: * Age \> 60 (on day of randomization) * DSM 5 criteria for Mild Neurocognitive Disorder ("MCI") * Willingness to provide informed consent * MADRS score of 10 or below * Availability of a study partner who has regular contact with the participant * Ability to read and communicate in English (with corrected vision and hearing, if needed) Exclusion: * Met DSM 5 criteria for Major Depressive Episode in past 10 years * Lifetime DSM 5 diagnosis of schizophrenia, bipolar disorder, or OCD * DSM 5 diagnosis of alcohol or other substances use disorder within the past 12 months * High risk for suicide * Significant neurological condition (e.g., stroke, seizure disorder, MS) * Unstable medical illness, (e.g., uncontrolled diabetes mellitus or hypertension) * Having taken a cognitive enhancer (acetylcholinesterase inhibitor or memantine) within the past 6 weeks. * Participants taking anticonvulsants, and other psychotropic medication (see exceptions below) that cannot be safely tapered and discontinued. The following psychotropic medications are allowed: i) any antidepressant; ii) zopiclone, trazadone, or a benzodiazepine if they have been taken at a stable dose for at least 4 weeks prior to study entry and; iii) gabapentin and pregabalin if they have been taken at a stable dose for at least 4 weeks prior to study entry AND if prescribed for chronic pain. * A pace-maker or other metal implants that would preclude safe use of tDCS. MDD Group Inclusion: * Age ≥ 65 (on day of randomization) * Meets DSM 5 criteria for one or more MDE(s)with: 1. an offset of 2 months to 5 years from the screening visit date. It is not necessary for this (these) episode(s) to have received medical attention OR 2. an offset of 5 years or more from the screening visit date. It is necessary that at least one MDE received medical attention (e.g., previously been on one or more antidepressant(s), saw a psychiatrist, primary care physician, or had a previous hospitalization). Also, the MDE must have occurred during the participant's adult life (i.e., at 18 years of age or older). * MADRS score of 10 or below * Willingness to provide informed consent * Availability of a study partner who has regular contact with the participant * Ability to read and communicate in English (with corrected vision and hearing, if needed) Exclusion: * Meets DSM 5 criteria for Major Neurocognitive Disorder ("dementia") * Lifetime DSM 5 diagnosis of schizophrenia, bipolar disorder, or OCD * DSM 5 diagnosis of alcohol or other substances use disorder within the past 12 months. * High risk for suicide. * Significant neurological condition (e.g., stroke, seizure disorder, MS) * Unstable medical illness (e.g., uncontrolled diabetes mellitus or hypertension) * Participants taking anticonvulsants, and other psychotropic medication (see exception below) that cannot be safely tapered and discontinued. In addition to any antidepressant, the following psychotropic medications are allowed if they have been taken at a stable dose for at least 4 weeks prior to study entry: zopiclone, trazodone, or a benzodiazepine; and gabapentin or pregabalin if prescribed for chronic pain. * Having taken a cognitive enhancer (acetylcholinesterase inhibitor or memantine) within the past 6 weeks. * A pace-maker or other metal implants that would preclude safe use of tDCS. * Received electroconvulsive therapy (ECT) within 6 months of baseline neruopsychological testing. Control group Inclusion: * Age \> 60 * MADRS score of 10 or below * Willingness to provide informed consent * Ability to read and communicate in English (with corrected vision and hearing, if needed) Exclusion: * Meets DSM 5 criteria for Minor or Major Neurocognitive Disorder * Any other lifetime DSM 5 diagnosis except for simple/specific phobias * Significant neurological condition (e.g., stroke, seizure disorder, MS) * Unstable medical illness, (e.g., uncontrolled diabetes mellitus or hypertension) * Participants taking anticonvulsants, and other psychotropic medication (see exception below) that cannot be safely tapered and discontinued. The following psychotropic medications are allowed if they have been taken at a stable dose for at least 4 weeks: zopiclone up to 15 mg/day; trazadone up to 150 mg/day; benzodiazepine at a dose of up to 3 mg/day lorazepam-equivalents; gabapentin and pregabalin (if prescribed for pain). * A pace-maker or other metal implants * Neuropsychological testing within the past 12 months
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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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Baycrest Centre for Geriatric Care
Toronto, Ontario, Canada
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Centre for Addiction and Mental Health
Toronto, Ontario, Canada
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St. Michael's Hospital
Toronto, Ontario, Canada
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Sunnybrook Heath Sciences Centre
Toronto, Ontario, Canada
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University Health Network
Toronto, Ontario, Canada
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Other studies related to the condition(s) this trial covers.
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