Fact CheckerSign in

NCT06120361Recruiting

The Swedish BioFINDER - Primary Care Study

Source: ClinicalTrials.gov · Last updated 6 Apr 2026

Brief summary (registry, in English)

The overall aim of the study is to improve the diagnostic accuracy of AD and cognitive impairment in primary care settings to ensure better care and treatment as well as facilitate correct referrals to specialized memory clinics. The investigators will strive to recruit diverse and representative populations of patients with subjective cognitive decline (SCD), mild cognitive impairment (MCI) and mild dementia. The specific aims of the study are to: 1. Improve the detection of mild cognitive impairment (MCI) and dementia in primary care. 2. Develop and evaluate cognitive tests, blood-based biomarkers and brain imaging methods that are suitable for accurate and early diagnosis of Alzheimer's disease (AD) in primary care. 3. To prospectively validate plasma AD biomarkers for diagnosis of patients with cognitive symptoms who are evaluated in primary care. 4. Determine whether blood AD biomarkers improve patient management in primary care.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1200 (estimated)
First submitted
2 Nov 2023
Start date
1 Jan 2020
Primary completion date
31 Dec 2028
Lead sponsor
Skane University Hospital
NCT number
NCT06120361

What you commit to

  • Study type: Observational
  • Planned participants: 1200
  • From 1 Jan 2020 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Already diagnosed dementia
  • Significant unstable systemic illness or organ failure that makes it difficult to participate.
  • Cognitive impairment with acute onset due to stroke
  • The cognitive impairment can with certainty be explained by another condition or disease such as significant anemia, infection, severe sleep deprivation, psychotic disorder, moderate-severe depression, alcohol abuse etc.

Other

  • Current significant alcohol or substance misuse.
  • Refusing investigation at the Memory clinic

Who the study is looking for

  • The patient seeks medical help because of cognitive symptoms experienced by the patient and/or informant OR The general practitioner suspects a progressive neurodegenerative disorder including, but not limited to, Alzheimer's disease, Lewy body disease, frontotemporal lobar degeneration or subcortical vascular cognitive impairment.
  • The main symptom is usually memory complaints, but could also be executive, visuo-spatial, language, or attention complaints.
  • Age ≥40 years
  • Subjective cognitive decline, mild cognitive impairment or mild dementia

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Primary care centers in Region Skåne
Coordinator of this site? Confirm its status
MalmöSwedenRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.