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Development of Cognitive Assessment Tools in Parkinson Disease

Development of Cognitive Assessment Tools in Parkinson Disease

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00556764
Acronym
ANAM
Enrollment
75
Registered
2007-11-12
Start date
2007-07-31
Completion date
2011-03-31
Last updated
2012-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease

Keywords

ANAM, Parkinson's

Brief summary

The main objectives of this protocol are as follows: 1. To assess the sensitivity and specificity of ANAM-PD in detecting cognitive status in patients with Parkinson disease (PD) and healthy controls (HC). 2. To validate the specific individual domains of the ANAM-PD cognitive battery by comparisons to available standardized cognitive evaluation scales administered to the patients with Parkinson disease with and healthy control subjects. 3. To evaluate the reliability of the ANAM-PD battery of tests by comparing repeated administrations of the ANAM-PD battery on a sub-set of subjects with Parkinson disease and healthy controls. 4. To characterize cholinergic neurotransmission through imaging the vesicular acetylcholine transporter binding with 123Iodobenzovesamicol (IBVM) and SPECT in PD patients and healthy controls.

Detailed description

General Design and Methods The overall goal of this proposal is to validate ANAM-PD as an assessment tool for cognitive status in PD. We propose a comprehensive strategy to evaluate the sensitivity and specificity of ANAM-PD in detecting cognitive changes in patients with a diagnosis of PD (n=50) and healthy controls (n=25). The specific testing domains of the ANAM-PD battery will be validated against standardized neuropsychological testing, described in detail below. The reliability of the ANAM-PD battery will be evaluated through a test-retest procedure in a subset of 50 subjects (25 PD and 25 HC). This strategy will enable us to evaluate the individual domains of the ANAM-PD computerized cognitive test and establish a battery as a standard test to efficiently measure cognitive changes in PD. We also propose to explore functional neuroimaging of the cholinergic system using \[123I\] IBVM and SPECT, a marker of vesicular acetylcholine transporter and a measure of the integrity of the cholinergic neuronal system. Identifying and validating ANAM-PD as an efficient tool for assessing cognitive changes in PD and exploring the cholinergic transporter system in PD through functional neuroimaging could predict sub-sets of PD patients 'at risk' for developing dementia and help elucidate the neurochemistry related to cognitive decline in PD

Interventions

DRUG[123I] IBVM and SPECT imaging

Subjects will be injected with up to 4 mCi of 123-I IBVM followed by SPECT imaging.

DRUGSubjects will undergo the 123-I IBVM imaging visit

Subjects will be injected with a bolus of up to 4 mCi of 123-I IBVM followed by serial SPECT imaging.

Sponsors

United States Department of Defense
CollaboratorFED
University of Oklahoma
CollaboratorOTHER
Institute for Neurodegenerative Disorders
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Inclusion and

Exclusion criteria

PD subjects Inclusion criteria: * The participant is 30 years or older. * Written informed consent is obtained. * Participants have a clinical diagnosis of Parkinson's disease based on Brain Bank Criteria. * Mini-mental status examination (MMSE) score ≥24 or significant cognitive dysfunction based clinical mental status exam. * Geriatric Depression Scales (GDS) ≤ 10. * For females, non-child bearing potential a negative urine or serum pregnancy test on day of 123-I IBVM injection.

Design outcomes

Primary

MeasureTime frame
The overall goal of this proposal is to validate ANAM-PD as an assessment tool for cognitive status in PD6 mos

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026