Intelligent Digital Tools for Screening of Brain Connectivity and Dementia Risk Estimation in People Affected by Mild Cognitive Impairment

Recruiting

• Conditions: Dementia; Cognitive Dysfunction; Mild Cognitive Impairment

• Registration Number: NCT05159661
• Lead Sponsor: Oslo University Hospital

Brief Summary

Every three seconds someone in the world develops dementia. There are over 50 million people worldwide living with dementia and by 2030 this figure is expected to reach 82 million. Besides time-consuming patient investigations with low discriminative power for dementia risk, current treatment options focus on late symptom management. By screening brain connectivity and dementia risk estimation in people affected by mild cognitive impairment, the European Union (EU) funded AI-Mind project will open the door to extending the 'dementia-free' period by offering proper diagnosis and early intervention. AI-Mind will develop two artificial intelligence-based digital tools that will identify dysfunctional brain networks and assess dementia risk. Personalised patient reports will be generated, potentially opening new windows for intervention possibilities.

Detailed Description

The aim of this study is to validate an AI based risk assessment tool for new clinical neurological data management in five clinical centres (Oslo OUS, Helsinki HUH, Madrid UCM, Rome IRCCS and Rome UCSC)). Today, around 50% of patients with mild cognitive impairment (MCI) are at risk to develop dementia, and that early risk signs include brain network disturbances as an expression of beginning synaptic dysfunction in the course of dementia development. This synaptic dysfunction can be registered by electrophysiological brain signals. The AI-Mind Connector will identify such disturbed brain network based on EEG technology. Brain networks patterns are identified among other mathematical possibilities by Graph theory. Classical machine learning and deep learning approaches of artificial intelligence will be used in automating these brain network identification processes in existing M/EEG data.

The secondly developed tool, the AI-Mind Predictor, will serve as an enriched Connector, a multimodal prediction method for risk estimation of dementia in MCI patients. In addition to Connector data, cognitive test results, genetic apolipoprotein E (APOE) allele and P-Tau-protein level information are integrated in the AI-Mind Predictor. The AI-Mind Predictor will discriminate between people at risk for further dementia development and non-at-risk. The anticipated high specific and sensitive AI-Mind Predictor results will be compared to state-of-the-art (SOA) approaches.

The cutting-edge AI-Mind model development and testing will be done by available anonymised and prospective pseudo-anonymised data collected at the 5 included clinical centres. Final adaptation, validation, and prototype development will be conducted by the hereby described collection of prospective data of a total 1000 MCI subjects, based on standardized clinical inclusion/exclusion criteria listed below. All patients will sign an informed consent before entering the study.

The patients will follow the AI-Mind protocol for a 2-year period in parallel with the SOA follow-up procedures at each hospital and country. The protocol includes repetitive M/EEG measurements, digitalised cognitive testing, and at the first visit a blood sample for APOE allele and p-Tau 181 analyses. At two of our clinical centres (HUH and UCM) clinical MEG is additionally offered for specific feature extraction for modelling by new EEG based AI-Mind Connector technology.

Importantly, AI-Mind's new data handling procedure will only use existing well-established, globally accessible and low-cost SOA technologies. With AI-Mind's new data processing approach the goal is to increase today's low predictive value (\<0.5) of SOA clinical dementia prediction, and proactively select, with higher accuracy than before, MCI patients at risk to be able to receive earlier clinical intervention. Thereby, AI-Mind wishes to contribute to delaying dementia development by detecting the risk already at the first visit when symptoms occur.

Study Timeline

• Study Start: 2021-03-01
• Study First Submitted: 2021-10-06
• Study First Submitted QC: 2021-12-10
• Study First Posted: 2021-12-16
• Status Verified: 2024-04
• Last Update Submitted: 2024-04-01
• Last Update Posted: 2024-04-02
• Primary Completion: 2025-09-30
• Study Completion: 2026-02-27

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 1000

Inclusion Criteria

• Male and female aged between 60 and 75 years
• MCI diagnosis with a MMSE >= 25
• or MCI diagnosis with MoCa >= 17

Exclusion Criteria

• Confirmed dementia
• History of cerebrovascular disease (i.e. stroke episodes)
• Alcohol Use Disorder Identification Test (AUDIT) score positive
• Severe medical disorders associated with cognitive impairment (organ insufficiencies, chronic infections, endocrinological disorders)
• Severe head trauma with structural brain lesion and/or previous brain surgery;
• Severe mental disorders; Schizophrenia, known Major depression or bipolar disorder
• Neuroimaging evidence of other potential causes of cognitive decline (e.g. subdural haematoma, malignancy)
• History of malignancy < 5 years;
• Recent use of psychotropic drugs including AChEI and Memantine (< 3 months);
• Participation in trials with experimental drugs.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
AI-Mind Connector with estimated specificity and sensitivity value > 0.9	2026	To validate the AI-Mind Connector as a biomarker for early brain network connectivity disturbance in at-risk patients.
AI-Mind Predictor with estimated specificity and sensitivity value > 0.9.	2026	To validate the AI-Mind Predictor as a diagnostic support tool for dementia risk evaluation. AI-Mind Predictor with higher prediction value for early dementia risk than current clinical practice.

Secondary Outcome Measures

Name	Time	Method
M/EEG connectivity measures	2026	To validate the accuracy of different M/EEG (connectivity) data features for predicting the risk of dementia
Clinical utility of Digital Cognitive Test compared to classical Neuropsychological test	2026	Report on the clinical utility of digital cognitive assessment tool for evaluation of cognitive function in people suspected of MCI and compare it to paper pencil classical neuropsychological test (NPT). The specific test (and domains) to be applied are Motor Screening Task (Attention and psychomotor speed), Delayed Matching to Sample (Memory), One Touch Stockings of Cambridge (Executive function), Paired Associates Learning (Memory), Pattern Recognition Memory (Memory), Reaction Time (Attention and psychomotor speed), Rapid Visual Information Processing (Attention and psychomotor speed), Spatial Working Memory (Executive function) and Match to Sample Visual Search (Attention and psychomotor speed). The score of the test domains of the digital cognitive test will be compared to equal domains measured through classical NPT.

Trial Locations

Locations (5)

Oslo University Hospital; 🇳🇴 Oslo, Norway

Helsinki University Hospital; 🇫🇮 Helsinki, Finland

Scientific Institute for Research, Hospitalization and Healthcare; 🇮🇹 Roma, Italy

Universidad Complutense de Madrid; 🇪🇸 Madrid, Spain

Università Cattolica del Sacro Cuore Campus di Roma; 🇮🇹 Roma, Italy