AD8 icon

AD8

Evidence Tier:CLINICAL GRADE

Validated in clinical trials

For:Clinicians & Healthcare ProfessionalsPatients & Caregivers

App Summary

The AD8 is an 8-item informant-based screening tool designed to help clinicians and families detect early cognitive changes associated with various forms of dementia. A validation study (N=255) demonstrated the tool's excellent ability to discriminate between individuals with and without dementia (AUC = 0.92), establishing it as a valid and reliable measure. The associated research concludes the AD8 is a brief, sensitive screening device, and scores indicating impairment warrant further formal assessment by a medical provider.

App Screenshots

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Detailed Description

Functionality & Mechanism

The AD8 application, developed by Washington University, implements the Ascertain Dementia 8-item Informant Questionnaire. The interface facilitates administration to an informant or, if unavailable, directly to the patient. The eight questions, which assess for intra-individual decline in memory, orientation, judgment, and function, can be self-administered or read aloud in person or by phone. The system provides integrated guidelines for administration and interpretation of results, with sessions typically completed in under three minutes.

Evidence & Research Context

  • A validation study in a clinical sample (N=255 patient-informant dyads) established strong concurrent validity with the Clinical Dementia Rating (CDR) (r=0.75), excellent internal consistency (Cronbach's alpha = 0.84), and high discriminative ability (AUC = 0.92).
  • The instrument's initial development demonstrated that a cut-off score of two endorsed items differentiates individuals with very mild dementia from those without, achieving 74% sensitivity and 86% specificity.
  • A subsequent psychometric analysis (N=403) using data from the National Health and Aging Trends Study confirmed a unidimensional measurement structure, robust reliability (Cronbach's alpha = 0.89), and no differential item functioning.
  • The instrument demonstrates robust reliability for both in-person and telephone administration (weighted kappa = 0.65-0.67) and very good interrater reliability (ICC = 0.80).

Intended Use & Scope

This application is designed for clinicians and researchers as a preliminary screening tool to detect early cognitive changes indicative of dementia. It facilitates the identification of individuals who require further diagnostic assessment. The AD8 is not a standalone diagnostic instrument; scores indicating impairment necessitate a comprehensive evaluation by a qualified medical provider.

Studies & Publications

3 publications

Peer-reviewed research associated with this app.

Validation Study

Item-level psychometrics of the Ascertain Dementia Eight-Item Informant Questionnaire

Ham et al. (2022) · PLoS ONE

Reliably measures dementia risk through structured informant questionnaire items.

The aim of this study is to evaluate the item-level psychometrics of the Ascertain Dementia Eight-Item Informant Questionnaire (AD-8) by examining its dimensionality, rating scale integrity, item fit statistics, item difficulty hierarchy, item-person match, and precision. We used confirmatory factor analysis and the Rasch rating scale model for analyzing the data extracted from the proxy versions of the 2019 and 2020 National Health and Aging
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Validation Study

Validity and reliability of the AD8 informant interview in dementia

Galvin et al. (2006) · Neurology

Accurately detects cognitive impairment and dementia through informant interviews.

Objective: To establish the validity, reliability, and discriminative properties of the AD8, a brief informant interview to detect dementia, in a clinic sample. Methods: We evaluated 255 patient–informant dyads. We compared the number of endorsed AD8 items with an independently derived Clinical Dementia Rating (CDR) and with performance on neuropsychological tests. Construct and concurrent validity, test–retest, interrater and intermodal
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AD8

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