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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05405075
Other study ID # ADRC-001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 1, 2021
Est. completion date June 30, 2026

Study information

Verified date July 2023
Source Banner Health
Contact Trisha Walsh
Phone 602.839.6029
Email Trisha.Walsh@bannerhealth.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The Arizona Alzheimer's Disease Research Center (ADRC) is the National Institute on Aging's (NIA's) first statewide AD Center (ADC), the only ADC in the Southwestern United States, and a leading example of statewide collaboration in biomedical research. It capitalizes on Arizona's strengths in brain imaging, genomics, computer science and biomathematics, the basic, cognitive and behavioral neurosciences, clinical, and neuropathological studies of AD, the discovery and evaluation of investigational treatments, and the study of normal cognitive aging.


Recruitment information / eligibility

Status Recruiting
Enrollment 550
Est. completion date June 30, 2026
Est. primary completion date June 30, 2026
Accepts healthy volunteers
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - Cognitively normal persons, individuals with mild cognitive impairment or dementia who are at least 40 years of age. - Willing to undergo health and cognitive assessments, and collection and banking of blood with venipuncture for genetic research, biomarker research, and DNA banking. Exclusion Criteria: - 1. Participants whose diagnosis is unclear and confounded by multiple possible factors are excluded. Participants with diagnoses of non-AD dementias are not excluded. 2. Participants whose primary diagnosis is cognitive impairment due to a penetrating or single severe closed head injury, multiple sclerosis, brain tumor, metabolic or toxic encephalopathy, post-infectious (e.g., viral encephalitis, bacterial meningitis), paraneoplastic, primary psychiatric illness, or otherwise not deemed relevant to the intent of the Alzheimer Disease Center program are excluded. 3. Procedure specific exclusion criteria also apply but this does not impact the participants ability to be included in the study.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Banner Alzheimer's Institute Phoenix Arizona

Sponsors (1)

Lead Sponsor Collaborator
Banner Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cognitive Status The ADRC uses a prospective, standardized, and longitudinal clinical evaluation of participants to determine their cognitive status. This includes tests that assess short and long term memory, ability to complete daily tasks, and processing of information. 12 months
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