Antipsychotic Discontinuation in Alzheimer's Disease (ADAD)

New York State Psychiatric Institute

Status and phase: Completed; Phase 4

Conditions: Psychotic Disorders; Alzheimer Disease; Aggression; Agitation

Treatments: Drug: risperidone

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00417482

#5598R

5R01AG021488 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

In patients with Alzheimer's disease (AD) who respond to antipsychotic treatment of psychosis and/or agitation/aggression, the relapse risk after discontinuation is not established. AD patients with psychosis and/or agitation/aggression receive 16 weeks of open risperidone treatment (Phase A). Responders are then randomized, double-blind, to one of three arms in Phase B: (1) continuation risperidone for 32 weeks, (2) risperidone for 16 weeks followed by placebo for 16 weeks, (3) placebo for 32 weeks. The primary outcome is time to relapse of psychosis/agitation.

Full description

This multicenter study (6 academic sites and 2 non-academic sites) involves treating AD patients (assisted living or nursing home patients, and outpatients) using an atypical antipsychotic, risperidone. In Phase A, 180 AD patients with psychosis and/or agitation/aggression receive open treatment with risperidone for 16 weeks. Responders are randomized, double-blind, to one of three arms in Phase B: (1) continuation risperidone for the next 32 weeks, (2) risperidone for the next 16 weeks followed by placebo for 16 weeks, or (3) placebo for the next 32 weeks. The primary hypothesis is that in the first 16 weeks of Phase B, relapse risk will be lower with continuation risperidone (Arms 1 + 2) compared to discontinuation on placebo (Arm 3). The secondary hypothesis is that in the second 16 weeks of Phase B, relapse risk will be lower with continuation risperidone (Arm 1) compared to discontinuation on placebo (Arm 2). For both randomized time periods, the proportions who relapse will be compared for interpretive support. This design provides useful data on the efficacy and side effects of longer term treatment with risperidone, and, in particular, critical information about the time to relapse and likelihood of relapse in patients switched from risperidone to placebo. This information is essential to guide the clinician toward optimal use of such medications in one of the most challenging types of patients: the AD patient with psychosis and/or agitation/aggression. The results of this study will also help to address Federal regulations urging early antipsychotic discontinuation in nursing homes.

Enrollment: 180 patients

Sex: All

Ages: 50 to 95 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Dementia, either sex, age 50-95 years
• Probable Alzheimer's disease
• Intellectual impairment present for at least 6 months
• Mini Mental State Exam (MMSE) score of 5-26 for outpatients and 2-26 for nursing home patients
• Availability of informant who has had direct contact with the patient for an average of at least once every week during the 3 months prior to study entry
• Meets Neuropsychiatric Inventory (NPI) criteria for either (1) psychosis, or (2) agitation/aggression
• Able to mobilize independently (if wheelchair-bound, the patient must be able to self-propel)
• Free of psychotropic medication (or able to tolerate washout) for at least 1 week prior to study entry. Low dose antidepressants and sedative/hypnotics allowed if they cannot be washed out and the dose remains stable for the study duration
• Expected to complete the study (including all efficacy evaluations) and be without major sensory impairment that would prevent participation in any aspect of the study

Exclusion criteria

• Current primary Axis I psychiatric disorder other than AD
• Substance abuse or dependence currently, or within the past year
• Dementia due to head trauma
• History of allergy to risperidone or intolerance to risperidone
• Diffuse Lewy body disease
• History of seizure disorder, infectious encephalitis, Parkinson's disease, central nervous system (CNS) neoplasm, tardive dyskinesia, stroke, transient ischemic attack (TIA) or uncontrolled atrial fibrillation
• Use of monoamine oxidase inhibitors (MAOIs) and unable to undergo 3-week washout; patients also may not take MAOIs for 2 weeks after completing the study
• In treatment with (a) depot antipsychotic within 2 weeks of the screening visit
• Untreated or incompletely treated hypothyroidism
• Active, unstable medical condition that requires active medication adjustment or surgery
• Need for electroconvulsive treatment (ECT)
• Significant risk for harm to themselves or others as a result of randomization to placebo
• History of malignant neoplasm during the last 5 years

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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180 participants in 3 patient groups

Risperidone-risperidone

Other group

Description:

Risperidone for 16 weeks followed by risperidone for 16 weeks

Treatment:

Drug: risperidone

Risperidone-Placebo

Other group

Description:

Risperidone for 16 weeks followed by placebo for 16 weeks

Treatment:

Drug: risperidone

Placebo-Placebo

Other group

Description:

Placebo for 16 weeks followed by placebo for 16 weeks

Treatment:

Drug: risperidone