Apathy Associated With Alzheimer's Disease

NCT ID: NCT00254033

Last Updated: 2017-04-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-10-31

Study Completion Date

2006-10-31

Brief Summary

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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.

Detailed Description

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Conditions

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Dementia Alzheimer Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Dextroamphetamine

Intervention Type DRUG

Methylphenidate

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
Minimum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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American Health Assistance Foundation

OTHER

Sponsor Role collaborator

Sunnybrook Health Sciences Centre

OTHER

Sponsor Role lead

Principal Investigators

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Krista L Lanctot, PhD

Role: PRINCIPAL_INVESTIGATOR

Sunnybrook Health Sciences Centre

Locations

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Sunnybrook Health Sciences Centre

Toronto, Ontario, Canada

Site Status

Countries

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Canada

References

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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.

Reference Type RESULT
PMID: 18591575 (View on PubMed)

Other Identifiers

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AHAF Grant Number: A2003-236

Identifier Type: -

Identifier Source: secondary_id

065-2003

Identifier Type: -

Identifier Source: org_study_id

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