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Davos Alzheimer's Collaborative Healthcare System Preparedness to Increase Cognitive Assessment Rates for Older Adults

Davos Alzheimer's Collaborative Healthcare System Preparedness to Increase Cognitive Assessment Rates for Older Adults

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06191952
Enrollment
500
Registered
2024-01-05
Start date
2023-02-01
Completion date
2024-02-01
Last updated
2024-01-11

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

Conditions

Alzheimer Dementia, Subjective Cognitive Decline

Keywords

Subjective Cognitive Decline, Mild Cognitive Impairment, Community Setting, Digital Cognitive Tests, Blood Biomarker

Brief summary

In this study the investigators explore a pragmatic strategy to increase cognitive screening rates in the community. The investigators will compare the monetary value of different combinations of SCD questionnaires, digital cognitive tests, and blood Alzheimer's Disease (AD) biomarkers to identify the best approach for primary care settings.

Detailed description

The investigators aim to perform a cluster-randomized study, exploring the effectiveness, efficiency, and acceptability of a pragmatic strategy to increase cognitive screening rates in the community. Participants will be older adults attending social and cultural centers in the greater Munich area. The investigators will compare the monetary value of different combinations of SCD questionnaires, digital cognitive tests, and blood AD biomarkers to identify the best approach for primary care settings. As secondary aims, qualitative interviews will be conducted with general practitioners (GPs) and their patients to explore the acceptability of the proposed new screening strategy; furthermore, the diagnostic utility of an artificial intelligence-based automated analysis of speech will be assessed. The initiative will not only generate novel insights into the optimal approach for large-scale cognitive screening in the general population, but also contribute to an urgently required cultural change in Germany, resulting in a sustainable solution for effective and efficient early recognition and prevention of dementia.

Interventions

DIAGNOSTIC_TESTCognigram

Cognigram (previously known as the Cogstate Brief Battery) is a brief, computer-administered cognitive test battery requiring about 20-25 minutes for administration, consisting of four cognitive tasks to measure psychomotor function, attention, working memory, and learning and memory. Eisai owns the commercial rights for Cognigram and has kindly agreed to offer the required licenses for the present project free of charge. Digital cognitive testing will take place in the respective social and care centers on a tablet which is not connected to the internet. Testing will be performed pseudonymized and data from the cognitive tests will be downloaded regularly by the study team and added to the database at LMU hospital.

DIAGNOSTIC_TESTSubjective cognitive decline questionnaire (SCD-Q)

The SCD-Q is a validated questionnaire assessing the presence of subjective cognitive deterioration in abilities such as memory, attention, language, and executive function. The scale includes 24 dichotomous questions (yes/no), evaluating decline in daily life during the last two years. The SCD-Q score ranges from 0 to 24, with higher scores indicating greater perceived cognitive change (cut-off classified as SCD equal or greater as 7).

DIAGNOSTIC_TESTblood-based biomarkers

Blood plasma and serum samples will be collected by the project staff according to standard operating procedures used at LMU Munich and subsequently processed and measured at the Department of Psychiatry and Psychotherapy to quantify the blood-based biomarkers for AD using Elecsys immunoassays running on a Cobas e402 analyzer. All test results (including the respective cut-off measurements for normal vs abnormal) will be forwarded directly to the participants' GPs. No further explanations and instructions will be provided to avoid any unwanted bias, and participants will only be informed about their results by their doctors. Roche has kindly offered to provide blood biomarker assays free of charge for the present project.

DIAGNOSTIC_TESTki:elements digital speech biomarker for cognition (ki:e SB-C)

The ki:elements digital speech biomarker for cognition (ki:e SB-C) can be collected remotely in fully automated telephone visits, taking 15 minutes to complete based on three specific assessments measuring learning and memory, processing speed, executive function, and language capabilities. The ki:e SB-C uses artificial intelligence and automatic speech analysis to process and transcribe speech, followed by an extraction of relevant features, combined into four subdomain and one global cognition score.

Sponsors

ki:elements
CollaboratorUNKNOWN
Hoffmann-La Roche
CollaboratorINDUSTRY
Eisai Limited
CollaboratorINDUSTRY
Johanniter-Unfall-Hilfe e.V.
CollaboratorUNKNOWN
University of Southern California
CollaboratorOTHER
Ludwig-Maximilians - University of Munich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Eligibility

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

Inclusion criteria

* age 65 years or older

Exclusion criteria

* younger than 65 years

Design outcomes

Primary

MeasureTime frameDescription
Proportion of participating individuals screening positive for SCDBaselineThe primary endpoint of this protocol is to assess the proportion of participating individuals aged 65 years or older screening positive for SCD during the intervention period who are referred to specialist evaluation, by study arm (intent to treat)

Secondary

MeasureTime frameDescription
Proportion of individuals with early-stage AD diagnosisBaselineProportion of individuals formally diagnosed with early-stage AD in a specialist clinic, by study arm
average time to diagnosis of ADBaselineAverage time to diagnosis of early-stage AD, by study arm
Qualitative interviewsBaselineQualitative participant and GP interviews on perceived changes/benefits/barriers, lessons learned, etc., per study arm
Correlation with speech analysis and other diagnostic testsBaselineCorrelation of ki:e SB-C global and domain cognitive scores with established AD neuropsychological tests and biomarkers (PET, cerebrospinal fluid, blood) and added value of automated speech assessment in routine cognitive assessment

Countries

Germany

Contacts

Primary ContactDr. Kurz
Psy.Alzheimerzentrum@med.uni-muenchen.de+4989440055863

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 24, 2026