Combined Brain Stimulation and Methylphenidate Treatment for Apathy in Dementia
Recruiting
Phase 2Interventional Study
Alzheimer s DiseaseAlzheimer Dementia (AD)Alzheimer DementiaAlzheimer DiseaseApathyApathy in Dementia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
12 (estimated)
Sponsor
Sunnybrook Health Sciences Centre · Other
Who this trial is looking for
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Answer a few quick questions to see if you may meet the eligibility requirements.
This study evaluates whether the combined treatment of methylphenidate and non-invasive brain stimulation, called intermittent theta burst stimulation, can effectively treat apathy in individuals with Alzheimer's disease or mixed AD/vascular dementia
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* Alzheimer's disease or mixed Alzheimer's disease and vascular disease
* MMSE score 10-28 inclusive
* Clinically significant apathy
* Stable dose of psychotropic medication
* Care partner must spend at least 10hrs/week with the participant
Exclusion Criteria:
* Major Depressi…
Inclusion Criteria:
* Alzheimer's disease or mixed Alzheimer's disease and vascular disease
* MMSE score 10-28 inclusive
* Clinically significant apathy
* Stable dose of psychotropic medication
* Care partner must spend at least 10hrs/week with the participant
Exclusion Criteria:
* Major Depressive Episode
* Clinically significant agitation, delusions, hallucinations
* Currently talking a dopaminergic agent other than methylphenidate
* Failure to clear the TMS adult safety scale (e.g. unapproved pacemakers, metallic implants, history of epilepsy)
* Central nervous system abnormalities (other than Alzheimer's disease) deemed clinically significant by study physician or seizures
* Any condition that in the opinion of the study physician, makes it medically unsafe for the patient to enroll in the trial
Contacts
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