Apathy Associated With Alzheimer's Disease

Phase 4

Completed

• Conditions: Dementia; Alzheimer Disease

• Registration Number: NCT00254033
• Lead Sponsor: Sunnybrook Health Sciences Centre

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2003-10
• Study First Submitted: 2005-11-10
• Study First Submitted QC: 2005-11-10
• Study First Posted: 2005-11-15
• Study Completion: 2006-10
• Status Verified: 2017-04
• Last Update Submitted: 2017-04-26
• Last Update Posted: 2017-04-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
Apathy Evaluation Scale-Caregiver (AES-C)
Addiction Research Centre Inventory (ARCI)

Secondary Outcome Measures

Name	Time	Method
Continuous Performance Test (CPT)
Neuropsychiatric Inventory (NPI)
Profile of Mood States (POMS)

Trial Locations

Locations (1)

Sunnybrook Health Sciences Centre; 🇨🇦 Toronto, Ontario, Canada