Digital Dementia Registry Bavaria: a multicenter, long-term registry of people with mild cognitive impairment and dementia and their family caregivers
Official title: Digital Dementia Registry Bavaria (digiDEM Bayern)
Run by University of Erlangen-Nürnberg Medical School · NCT07721701 · Data updated 2026-11-12
This registry will collect long-term health and care data from people with mild cognitive impairment or dementia in Bavaria and their caregivers to understand how dementia progresses and how care is provided.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | University of Erlangen-Nürnberg Medical School Academic / other |
| Locations | 12 sites (Aschaffenburg and 11 other locations) |
| Status | Recruiting |
| Started | August 10, 2020 |
| Main results expected | December 31, 2031 |
| Study ends | December 31, 2031 |
| Registry record updated | July 23, 2026 |
| Trial ID | NCT07721701 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with any type of MCI or dementia (per ICD-10), living in Bavaria and not in a nursing home, able to participate in long-term follow-up.
✕Probably not a fit
Individuals without dementia or MCI, or those residing permanently in nursing homes, may not benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
DigiDEM Bayern is a multicenter, prospective, longitudinal registry study conducted across Bavaria to map the clinical complexity, progression, and care needs of people with MCI and various forms of dementia, including Alzheimer’s disease and vascular dementia. The study enrolls participants from urban and rural areas who live at home and follow them over time to collect health outcomes, including cognitive and functional status, care arrangements, and quality of life. Data are gathered to improve understanding of disease trajectories and inform care planning and health system responses. Exclusion criteria include advanced non-communicative conditions, nursing home residence, certain psychiatric diagnoses, and sensory impairments that would limit participation.
Why it matters
Potential benefit: Better understanding of dementia progression and care needs could inform resource planning and support services for patients and caregivers.
How similar studies have gone: Other dementia registries and observational cohorts have yielded meaningful insights into progression and care needs, supporting the value of this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * People with an MMSE score of 24-30 points and an additional MoCA score of 0-23 points * People with an MMSE score of 15-23 points * Living in a home environment * All types of MCI and dementia according to the ICD-10 classification (F06.7, F00-F03) * Main residence in Bavaria * All age groups Exclusion Criteria: * People with an MMST score of 24-30 points and an additional MoCA score of 24-30 points * People with an MMST score of 0-14 points * Permanent residence in a nursing home * Psychiatric diagnoses (among others depression, schizophrenia, addiction) * Deafness and/or blindness * Aphasia
Where it's running
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Klinikum Aschaffenburg-Alzenau
Aschaffenburg, Germany Recruiting -
Schön Klinik Bad Aibling
Bad Aibling, Germany Recruiting -
RHÖN-KLINIKUM Campus Bad Neustadt
Bad Neustadt an der Saale, Germany Recruiting -
Klinikum Bayreuth
Bayreuth, Germany Recruiting -
Klinikum Coburg, Regiomed Zentrum für Altersmedizin
Coburg, Germany Recruiting -
Kliniken Am Goldenen Steig
Freyung, Germany Recruiting
Show 6 more locations
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Marion von Tessin Memory-Zentrum
München, Germany Recruiting -
Schön Klinik München Schwabing
München, Germany Recruiting -
Klinikum Neumarkt
Neumarkt, Germany Recruiting -
Klinikum Nürnberg
Nuremberg, Germany Recruiting -
Klinik und Poliklinik für Psychiatrie Regensburg
Regensburg, Germany Recruiting -
Böhm-Peters - Praxis für Psychiatrie, Psychotherapie und Neurologie
Rosenheim, Germany Recruiting
Study contacts
- Study coordinator: Peter L. Kolominsky-Rabas, Univ.-Prof. Dr. med.
- Email: peter.kolominsky-rabas@fau.de
- Phone: +49 9131 85-35855
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Hyperspectral retinal imaging to detect Alzheimer’s and other neurodegenerative changes
This project will test whether a special retinal camera that scans many wavelengths of light can detect signs of Alzheimer’s and other neurodegenerative diseases in people with dementia or at risk.
-
Predicting disease progression in dementia using biomarkers and modeling
This study is trying to create a tool that helps predict how dementia will progress in people with mild cognitive impairment and different types of dementia, like Alzheimer's and Lewy Body Disease, by looking at brain scans, body fluids, and mental tests.
-
BRAIN App program to support communication and engagement for people with dementia
This program tests whether the BRAIN App can improve communication, mood, and quality of life for people aged 65 and older with dementia living in long-term care, with training and support for family members and staff.
-
Investigating new blood tests for diagnosing memory disorders
This study is testing new blood tests to see if they can help diagnose memory disorders like mild dementia and Alzheimer's better than the current method that uses spinal fluid.
-
Improving early diagnosis of dementia in primary care
This study is trying to find better ways to diagnose Alzheimer's and other memory problems early in people visiting their primary care doctors.
-
Connecting Through Music for people with dementia
The trial tests a music-based program led by volunteers or staff to help residents with dementia in long-term care facilities, aiming to ease behavioral symptoms and improve caregiving efficiency.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.