Electroconvulsive Therapy (ECT) for Agitation in Dementia (AD)
Launched by BRENT FORESTER · Apr 23, 2019
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring the use of Electroconvulsive Therapy (ECT) in combination with usual care to help reduce severe agitation in patients with various types of dementia, including Alzheimer’s Disease. Agitation can involve behaviors like hitting, kicking, or yelling, which can be distressing for both the patients and their families. The researchers want to see if ECT+usual care can safely improve these symptoms and make daily life easier for patients suffering from moderate to severe dementia.
To participate in the trial, individuals must be at least 40 years old and have a diagnosis of dementia, such as Alzheimer’s or vascular dementia, along with significant agitation that hasn’t improved with standard medications. It’s important that participants are medically stable and can understand English. Family members or legal representatives will need to provide consent for those who are unable to do so. This study is currently recruiting participants, and it’s a chance for patients to potentially receive a new treatment option that could help manage their symptoms better.
Gender
ALL
Eligibility criteria
- • Inclusion Criteria
- • 1. Diagnosis of Dementia, of the following subtypes,
- • 1. Alzheimer's dementia, according to NIA-AA Criteria for dementia
- 2. Vascular dementia based on:
- • i. History consistent with insidious onset of illness and gradual clinical decline ii. MRI evidence of microvascular ischemic disease (microinfarcts) iii. Physical and neurological examination do not indicate current or prior stroke c. Frontotemporal dementia d. Dementia with Lewy Bodies
- • 2. Mini Mental Status Exam (MMSE) less than or equal to 15
- • 3. Cohen-Mansfield Agitation Inventory Nursing Home Version (CMAI) score of 5 or more on at least one item or score of 4 on two items of aggression or physical nonaggression that holds potentially dangerous consequences including hitting (including self), kicking, grabbing onto people, pushing, throwing things, biting, scratching, spitting, hurting self or other, tearing things or destroying property, making physical sexual advances, trying to get to a different place, or intentional falling (items 1-11, 14, 15) OR one score of 5 or more in items of verbal aggression including screaming, making verbal sexual advances, and cursing or verbal aggression (items 22-24).
- • 4. At least one failed pharmacological intervention to manage behavioral symptoms
- • 5. Medically stable for safe administration of ECT verified by standard physical examination, urinalysis and serum chemistries and brain imaging when clinically indicated
- • 6. Comprehension of English language
- • 7. Authorized legal representative able and willing to give informed consent
- • 8. Age 40 and above
- Exclusion Criteria:
- • 1. Current diagnosis of co-morbid delirium, measured by the Confusion Assessment Measure (CAM) and by clinical diagnosis
- 2. Diagnosis of vascular dementia due to stroke, based on:
- • History consistent with abrupt onset and step-wise progression of cognitive and functional decline
- • MRI scan within the past 12 months demonstrating evidence of hemorrhagic and embolic stroke
- • Physical and neurologic examination consistent with current or prior stroke
- • 3. Lifetime or current diagnosis of Schizophrenia, Bipolar Disorder or Schizoaffective Disorder
- • 4. Active substance use disorder within past 6 months
- • 5. Treatment with ECT or other neurostimulation therapies (e.g., TMS or vagal nerve stimulation) within the past 3 months
About Brent Forester
Brent Forester is a distinguished clinical trial sponsor renowned for his commitment to advancing psychiatric research and innovative treatment methodologies. With a robust background in neuroscience and clinical psychiatry, he leads initiatives focused on developing cutting-edge therapies for mood and anxiety disorders. His leadership is characterized by a collaborative approach, fostering partnerships with leading academic institutions and pharmaceutical companies to ensure the highest standards of scientific rigor and ethical conduct in clinical trials. By prioritizing patient safety and efficacy, Brent Forester is dedicated to translating research findings into meaningful clinical advancements that improve the lives of individuals facing mental health challenges.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rochester, Minnesota, United States
Belmont, Massachusetts, United States
Grand Rapids, Michigan, United States
Atlanta, Georgia, United States
Glen Oaks, New York, United States
Patients applied
Trial Officials
Brent P Forester, MD, MSc
Principal Investigator
Mclean Hospital
George Petrides, MD
Principal Investigator
Northwell Health
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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