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Digital screening for the Assessment of Cognitive Abilities (digiDEM-SCREEN)

Digital screening for the Assessment of Cognitive Abilities (digiDEM-SCREEN) - digiDEM-SCREEN

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033764
Enrollment
135
Registered
2024-04-04
Start date
2024-04-24
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

The purpose of the screening test is to assess possible initial signs of cognitive impairment and to find indications of a potential dementia disorder. No diagnosis is made on the basis of the screening result itself. If the result is abnormal, the patient is referred to a specialist for further diagnostic clarification.

Interventions

Group 1: Study participants are cognitively healthy people, people with mild cognitive impairment (MCI) or people with dementia in an early stage, who all complete the following study procedure. In a

Sponsors

Friedrich-Alexander-Universität Erlangen-Nürnberg, Interdisziplinäres Zentrum für Health Technology Assessment und Public Health (IZPH)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Full capacity to consent According to study group: - No cognitive impairment (MMST > 26) - Presence of mild cognitive impairment (MCI) - Presence of dementia at an early stage (assessment by the attending physician) Sufficient knowledge of the German language to use the app

Exclusion criteria

Exclusion criteria: Non-existent capacity to consent Advanced dementia (MMST < 10) Deafness Blindness Motor impairments Psychiatric illnesses (except dementia, if applicable)

Design outcomes

Primary

MeasureTime frame
The screening test has a specificity of at least 0.90 with a sensitivity of at least 0.5.

Secondary

MeasureTime frame
The digital screening test shows a high level of agreement (Pearson r at least 0.7) with the existing cognitive test procedure MoCA. This test for the hypothesis r > 0.3 (r=0.3 as an irrelevant variable) can be performed with a sample size of n=42 with a statistical power of 95%.

Countries

Germany

Contacts

Public ContactPeter L. Kolominsky-Rabas

Friedrich-Alexander-Universität Erlangen-Nürnberg, Interdisziplinäres Zentrum für Health Technology Assessment und Public Health (IZPH)

peter.kolominsky-rabas@fau.de+49 9131 85-35855

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026