Title of the cohortLongitudinal Urban Cohort Ageing Study
Name of Principal InvestigatorTitle | Dr. |
First name | Ulrike |
Last name | Dapp |
Address of institution where award is heldInstitution | ertinen-Haus, Centre for Geriatrics and Gerontology, Research Department |
Street Address | Sellhopsweg 18-22 |
City | Hamburg |
Postcode | 22459 |
Websitewww.geriatrie-forschung.de
Funding source1. The cohort includes, or expects to include, incidence of the following conditions
1. The cohort includes, or expects to include, incidence of the following conditions- Alzheimer’s disease and other dementias
- Neurodegenerative disease in general
When studies on the above condition(s) are expected to become possible
2a. Stated aim of the cohortTo enlighten the black box of the ageing process by establishing a longitudinal cohort making use of a randomised controlled trial (RCT) carried out in 2000 with over 3,300 independent senior citizens in the community of Hamburg. Information about pre-clinical markers for healthy ageing vs. the development of functional decline, has been collected multidimensionally in an interdisciplinary process since 2000.
2b. Features distinguishing this cohort from other population cohorts
3a. i) Number of publications that involve use of cohort to date0
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 recruitmentAge in years from: | 60 |
To (‘until death’ if applicable): | 98 |
4b. Study criteria: inclusion criteriapatients 60 + years in participating general practices (GP) in Hamburg in year 2000
4c. Study criteria: exclusion criteriapatients needing help in basic activities of daily life; patients obtaining nursing care according to the German long-term care insurance (Pflegeversicherung I-III); patients with cognitive impairment; patients with terminal disease and/or patients unable to understand German
5. Size of the cohort (i.e. number of participants enrolled)1,000 – 5,000 participants
6a. Measures used to characterise participantsmultidimensional dataset using self-administered questionnaires in waves with whole cohort plus multidimensional assessments with randomly selected subgroups
6b. Additional measures for participants with a clinical disorder
6c. Are there defined primary and secondary endpoints (e.g. defined health parameters)functional status, nursing care (Pflegestufe), death
9a. Does the study include a specialised subset of control participants
9b. If yes, description of specialised subset of control participants
10a. i) Data collection start date
10a. ii) Data collection end date
10a iii) Data collection for this study is- Data collection ongoing
- Data analysis ongoing
10b. Plans to continue the cohort study beyond the current projected end date- Yes – intend to apply for funding
12. System in place to enable re-contact with patients for future studies
13a. Format and availability of data stored in a database
13b. Format and availability of data held as individual records
14a. Are data available to other groups
14b. Access policy/mechanisms for access if data are available to other groups- Other criteria (please specify)
- only for LUCAS consortium partners until end of funding
15. Data sharing policy specified as a condition of useData made publicly available after a specified time point
16a. Are tissues/samples/DNA available to other groups
16b. i) Description of available tissues/samples/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
17. Is information on biological characteristics available to other groups Types: Population Cohorts
Member States: Germany
Diseases: Alzheimer's disease & other dementias, Neurodegenerative disease in general
Years: N/A
Database Categories: N/A
Database Tags: N/A
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