Apathy Associated With Alzheimer's Disease
The Role of the Dopaminergic Brain Reward System in Apathy Associated With Alzheimer's Disease
2 other identifiers
interventional
40
1 country
1
Brief Summary
Apathy, or lack of motivation, affects up to 80% of Alzheimer's disease (AD) patients. These amotivational symptoms increase patient reliance on caregivers, increase caregiver burden and distress, and increase the risk of patient institutionalization. Only 50% of patients with apathy respond to current treatment with cholinesterase inhibitors. The mechanism of apathy in AD is unknown hampering rational treatment. Our proposed pilot study will provide initial data required to develop an amphetamine challenge paradigm to probe the brain reward system. These results will be used to develop a larger study evaluating the role of the brain reward system in apathy in AD and link this information with pharmacologic treatment. AD is a complex neurobiological illness that needs to be understood at several levels to optimize treatment. At a neurochemical level, one has to identify the neurotransmitter abnormalities that accompany the clinical symptoms. The neurochemical level of analysis provides the link between pathology and symptoms and, for now, is the only avenue for biological therapies. Next, one has to translate knowledge of neurochemical abnormalities to practical treatments for the symptoms of AD. This pilot will allow us to develop a study that can address both of these goals. Furthermore, the larger study will further define the emerging concept of apathy as a syndrome and has broader implications for apathy in many other neuropsychiatric diseases.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_4
Started Oct 2003
Typical duration for phase_4
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2003
CompletedFirst Submitted
Initial submission to the registry
November 10, 2005
CompletedFirst Posted
Study publicly available on registry
November 15, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2006
CompletedApril 28, 2017
April 1, 2017
November 10, 2005
April 26, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Addiction Research Centre Inventory (ARCI)
Apathy Evaluation Scale-Caregiver (AES-C)
Secondary Outcomes (3)
Profile of Mood States (POMS)
Continuous Performance Test (CPT)
Neuropsychiatric Inventory (NPI)
Interventions
Eligibility Criteria
You may qualify if:
- age \> 55 years
- meet DSM-IV criteria for primary degenerative dementia
- meet NINCDS-ARDA criteria for probable Alzheimer's Disease of at least one year's duration
- mild to moderate cognitive impairment (Global Deterioration Scale GDS \<6, Mini-Mental State Examination \>10
- on a stable dose of a cholinesterase inhibitor for at least 3 months
- apathetic group only: Neuropsychiatric Inventory (NPI) Apathy subscale score \>=2
You may not qualify if:
- abnormal biochemical screening: blood cell count, vitamin B12, thyroid function tests, and syphilis screening tests
- significant medical illness or other medical/neurological conditions which diminish cognitive function
- evidence of seizure disorder
- an Hachinski ischemic score \>3 indicating vascular dementia
- a brain computed tomographic (CT) scan revealing focal lesions, or inconsistent with AD
- electrocardiographic, laboratory or physical evidence of significant cardiovascular disease
- presence of premorbid or current psychiatric diagnosis including: major depression, schizophrenia, psychotic symptoms of a severity likely to provoke violent or dangerous behaviour (i.e., command hallucinations to harm people or persecutory delusions that provoke violent reactions)
- current or past psychoactive substance abuse or dependence (including alcohol, excluding nicotine)
- contraindications to receiving dextroamphetamine or methylphenidate
- have had administration of a depot neuroleptic injection within one treatment cycle of the first visit
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sunnybrook Health Sciences Centre
Toronto, Ontario, M4N 3M5, Canada
Related Publications (1)
Lanctot KL, Herrmann N, Black SE, Ryan M, Rothenburg LS, Liu BA, Busto UE. Apathy associated with Alzheimer disease: use of dextroamphetamine challenge. Am J Geriatr Psychiatry. 2008 Jul;16(7):551-7. doi: 10.1097/JGP.0b013e318170a6d1.
PMID: 18591575RESULT
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Krista L Lanctot, PhD
Sunnybrook Health Sciences Centre
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
November 10, 2005
First Posted
November 15, 2005
Study Start
October 1, 2003
Study Completion
October 1, 2006
Last Updated
April 28, 2017
Record last verified: 2017-04