Title of the cohort

Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability

Acronym for cohort

FINGER

Name of Principal Investigator
Title Docent, Ass Professor
First name Miia
Last name Kivipelto
Address of institution where award is held
Institution Univeristy of Eastern Finland
Street Address Yliopistonranta 1 B
City Kuopio
Postcode 70211
Country
  • Finland
Website

www.thl.fi/finger

Contact email

miia.kivipelto@uef.fi

Funding source

Academy of Finland
Kuopio Univeristy Hospital
Univeristy of Eastern Finland
Alzheimer Association USA

1. The cohort includes, or expects to include, incidence of the following conditions
  • Alzheimer’s disease and other dementias
When studies on the above condition(s) are expected to become possible
  • 2011 – 2015
2a. Stated aim of the cohort

Multimodal intervention study in subjects with increased risk for Alzheimer’s disease and with slight memory impairment.

2b. Features distinguishing this cohort from other population cohorts

Multimodal 2-year intervention study in subjects with increased risk for Alzheimer’s disease and with slight memory impairment.

3a. i) Number of publications that involve use of cohort to date
3a. ii) Up to three examples of studies to date (PI, Institution, Title of Study)
3b. Publication list/link to where data or publications are accessible (if available)
3c. Information (i.e. research findings) expected to be gained from the population cohort
4a. Study criteria: age range of participants at recruitment
Age in years from: 60-75 years
To (‘until death’ if applicable):
4b. Study criteria: inclusion criteria

High dementia risk score (Kivipelto et al 2006) and objective evidenced memory /
cognitive impairment

4c. Study criteria: exclusion criteria

Dementia, any major disease preventing participation in the intervention

5. Size of the cohort (i.e. number of participants enrolled)
  • 1,000 – 5,000 participants
6a. Measures used to characterise participants

Demographic, health, cognition, functional capacity, cardiovascular fitness parameters…

6b. Additional measures for participants with a clinical disorder
6c. Are there defined primary and secondary endpoints (e.g. defined health parameters)
  • No
7. Study design
  • Other (please specify)
  • Randomized intervention study
8. Cases matched by
  • Age
  • Sex
9a. Does the study include a specialised subset of control participants
  • No
9b. If yes, description of specialised subset of control participants
10a. i) Data collection start date

01-09-2009

10a. ii) Data collection end date

31-12-2013

10a iii) Data collection for this study is
  • Data collection ongoing
10b. Plans to continue the cohort study beyond the current projected end date
  • Yes – intend to apply for funding
11. Data collected
  • Only through the study
  • Through links to medical records
  • Through links to other records or registers (such as dental records, police records etc). Please specify
  • ###VALUE###
12. System in place to enable re-contact with patients for future studies
  • Yes (participants have given permission to be re-contacted via the PIs to ask if they would participate in further studies)
13a. Format and availability of data stored in a database
Yes/No % available
Data summarised in database
Database is web-based  Yes
Database on spreadsheet
Database is on paper  No
Other (specify)

 

Language used:

Finnish /English

13b. Format and availability of data held as individual records
Yes/No % available
Data held as individual records  Yes
Data is web-based Yes
Data held on computer based records  Yes
Data held on cards
Other (specify)

 

Language used:

Finnish /English

14a. Are data available to other groups

Yes

14b. Access policy/mechanisms for access if data are available to other groups
  • Access through collaboration with PI only
15. Data sharing policy specified as a condition of use
  • No requirement to make data publicly available
16a. Are tissues/samples/DNA available to other groups

Yes

16b. i) Description of available tissues/samples/DNA
  • Living donors:blood
  • Living donors: blood derivatives
  • Living donors: DNA
16b. ii) Form available tissues/samples/DNA are supplied in
16b. iii) Is the access policy/mechanism for obtaining samples the same as that for obtaining data

Yes

17. Is information on biological characteristics available to other groups
  • No

Types: Population Cohorts
Member States: Finland
Diseases: Alzheimer's disease & other dementias
Years: 2011
Database Categories: N/A
Database Tags: N/A

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