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Computational Tools for Early Diagnosis of Memory Disorders

Virtual Physiological Human (VPH) Dementia Research Enabled by IT - Prospective Cohort Kuopio

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02050464
Acronym
ProsKuopio
Enrollment
126
Registered
2014-01-30
Start date
2013-12-31
Completion date
2017-04-30
Last updated
2017-05-04

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

Conditions

Alzheimer Disease, Dementia, Vascular, Frontotemporal Dementia, Mild Cognitive Impairment

Keywords

Alzheimer Disease, Frontotemporal Dementia, Dementia, Vascular, Mild Cognitive Impairment, Diagnosis, Risk factors, Biomarkers, AD, FTD, VAD, MCI

Brief summary

The Virtual Physiological Human: DementiA Research Enabled by IT (VPH-DARE@IT) is a four-year IT-project funded through the European Union (EU). The project consortium involves a total of 21 universities and industrial partners from 10 European countries. The project delivers the first patient-specific predictive models for early differential diagnosis of dementia and their evolution. An integrated clinical decision support platform will be validated / tested by access to a dozen databases of international cross-sectional and longitudinal studies. As a part of the VPH-DARE@IT project, a new prospective cohort will be collected in Kuopio. This prospective cohort will be used to test further the modeling approaches and tools developed by using the retrospective databases.

Detailed description

The Virtual Physiological Human: DementiA Research Enabled by IT (VPH-DARE@IT) is a four-year IT-project funded through the European Union (EU). The project will develop multiscale models of the ageing brain in order to account simultaneously for the patient-specific biochemical, metabolic and biomechanical brain substrate, as well as for genetic, clinical, demographic and lifestyle determinants. An integrated clinical decision support platform will be validated and tested by access to a dozen databases of international cross-sectional and longitudinal studies. Modeling approaches developed by using the retrospective databases will be tested using a new prospective cohort that will be collected in Kuopio as a part of the VPH-DARE@IT project. The study population at university of Eastern Finland (UEF) will be a total of 120 subjects: 20 healthy controls (HC), 20 mild to moderate Alzheimer's disease (AD) patients, 20 vascular dementia (VAD) patients, 20 fronto-temporal dementia (FTD) patients and 40 subjects with mild cognitive impairment (MCI). This study is referred as VPH-DARE@IT Prospective study in Kuopio or ProsKuopio.

Interventions

None listed

Sponsors

University of Sheffield
CollaboratorOTHER
VTT Technical Research Centre of Finland
CollaboratorOTHER
Klinik Hirslanden, Zurich
CollaboratorOTHER
Sheffield Teaching Hospitals NHS Foundation Trust
CollaboratorOTHER
University of Eastern Finland
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

Inclusion criteria for subjects with dementia (AD, VAD, FTD) - The inclusion criteria will be based on international research criteria: * Diagnosis of probable AD according to National Institute of Neurological and Communicative Disorders and Stroke Alzheimer's (NINCDS-ADRDA) criteria (McKhann et al.1984) and diagnosis of prodromal AD according to Dubois et al., 2007 criteria * Diagnosis of FTD according to the clinical diagnostic criteria of Neary et al., 1998 * Diagnosis of VAD according to diagnostic criteria for research studies by the NINDSAIREN International Workshop (Román et al., 1993) Inclusion criteria for subjects with MCI * Referral because of cognitive impairments * Diagnosis criteria for amnestic and nonamnestic MCI (Petersen, 2004, Petersen and Morris, 2005) Inclusion criteria for control subjects * Mini-mental state examination (MMSE) score above or equal to 27 * Overall score on the Clinical Dementia Rating (CDR) scale of 0

Design outcomes

Primary

MeasureTime frameDescription
Sensitivity, specificity and accuracy of models for diagnosis of memory disordersduring a single visit, i.e., day 1 and for one study group (MCI) after 18 month follow-upThe models developed the VPH-DARE project will be tested in this prospective cohort. Sensitivity, specificity and accuracy of the model will be tested in differential diagnosis between the study groups as well as the accuracy of prediction cognitive decline as measured by neuropsychological test battery in the MCI group.

Countries

Finland

Outcome results

None listed

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