Personalising care for memory and thinking difficulties
This study searches for genetic and other biological markers that could help guide care for dementia or mild thinking difficulties.
Learning by observing or collecting information · Study reference: JPRN-UMIN000039487
Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓
This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.
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Results reported
- Start (reported date)
- 2020-03-01
- Study finished (reported date)
- 2025-06-30
Planned dates can move. A study finishing does not tell us when a paper will be published.
Read the results reported in the registry
Changes we have recorded
- 2026-10-11 — recruiting
These are dates we observed a change, not necessarily the dates it happened.
Papers connected to this study
No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.
Who can join?
Age 20years-old and over · Ask the team who can join
These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.
Read all the rules for taking part
Sex eligibility reported by registry: male and female
Full study name & original research details
Official study title
Search and verification test of genome and bio-markers for the purpose of constructing an individualized treatment algorithm for dementia and mild cognitive impairment - Precision medicine research in dementia and mild cognitive impairment
Short title used by the registry
Search and verification test of genome and bio-markers for the purpose of constructing an individualized treatment algorithm for dementia and mild cognitive impairment
Original description
Conditions reported: Major or Mild Neurocognitive Disorder Due to Alzheimer's Disease, Major or Mild Frontotemporal Neurocognitive Disorder, Major or Mild Neurocognitive Disorder with Lewy Bodies, Major or Mild Vascular Neurocognitive Disorder, Major or Mild Neurocognitive Disorder Due to Traumatic Brain Injury, Major or Mild Neurocognitive Disorder Due to Prion disease, Major or Mild Neurocognitive Disorder Due to Parkinson's Disease, Major or Mild Neurocognitive Disorder Due to Huntington's Disease, Major or Mild Neurocognitive Disorder Due to Multiple System Atrophy, Senile Dementia or Mild Cognitive Impairment of the Neurofibrillary Tangle Type, Major or Mild Neurocognitive Disorder Due to Normal Pressure Hydrocephalus, Cognitive Impairment Due to Delirium
Registry records for this study
Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.
- JPRN · JPRN-UMIN000039487 ↗ — Recruiting; WHO ICTRP processed 2026-06-29; checked 2026-10-11
- Study type
- Observational
- Interventions
- Not reported
- Phases
- Not selected
- Sponsor
- Kansai Medical University
- Start date reported by registry
- 2020-03-01 (reported)
Registry updated: Not reported · Status last verified by the registry submitter: Not reported
Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.
Contact the research team
Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.
Yuji Murase · 06-6992-1001 · murasey@takii.kmu.ac.jp
Study locations
Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.
Facility not reported
Japan
Status not reportedThe original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.