Title of the registerNational Data Bank for Alzheimer's Disease
Name of Principal Investigator - Title
Name of Principal Investigator - First name
Name of Principal Investigator - Last name
Address of institution -Institution
Address of institution - Street address
Address of institution - City
Address of institution - Postcode
Q1a. Please indicate below if your cohort includes or expects to include, incidence of the following conditions?Neurodegenerative disease in general
Q2. In a single sentence, what is the stated aim of your register?French National Alzheimer Database (BNA) aim to provide epidemiological data as well as activity indicators within the network of the french memory center and private specialist
Q2b. What distinguishes this register from other disease registers?The register is totally integrated in the clinical activity of the center
Q3a. i) Number of publications that involve use of your register to date
Q3a. ii) Please give up to three examples of studies to date (PI, Institution, Title of Study)
Q3b. If data on research outputs are already available please paste the publication list/other data or provide a link to where these data are publicly available?Evolution of the Antidepressant Prescribing in Alzheimers Disease and Related Disorders Between 2010 and 2014 : Results from the French National Database on Alzheimers Disease (BNA). Journal of Alzheimers
Q3c. If no research has been done as yet, please explain in a few sentences what information (i.e. research findings) you expect will be gained from the register
Q4a. Study criteria: what is the age range of participants? Age in years: from
Q4a. Study criteria: what is the age range of participants? Age in years: to
Q4b. Study criteria: what are the inclusion criteria?Patients from French memory centres and voluntary independent physicians.
Q4c. Study criteria: what are the exclusion criteria?
Q5. What is the size of the register (i.e. how many patients have been enrolled)?More than 10,000 clinical cases
Q6a. Please describe what measures are used to characterise participantsDiagnosis according to the clinician point of view (ICD10)
Q6b. Are there defined primary and secondary endpoints (e.g. defined health parameters)?
Q7a. i) Is the register of fixed duration?
Q7a. ii) Please enter the data collection start date
Q7a. iii) Please enter the data collection end date
Q7b. Could you provide some information about the data collection for this register?Data collection ongoing|Data analysis ongoing
Q8. Funding of the register - How is the register funded?Direction générale de loffre de soins
Q8. Funding of the register - Is this funding expected to continue
Q8. Funding of the register - If so, for how long (months)?at least till the end of the national plan
Q9. Could you provide information about data sweeping? - How many data sweeps have taken place?
Q9. Could you provide information about data sweeping? - When was the most recent data sweep?
Q9. Could you provide information about data sweeping? - When is the next data sweep?
Q9. Could you provide information about data sweeping? - How many more data sweeps are planned on current funding? e.g 0,1,2…..
Q9. Could you provide information about data sweeping? -How many more data sweeps are planned in total (with funding and with funding yet to be secured) e.g. 0,1,2…
Q10. Is the clinical (phenotypic) information that is held in the register from patients and other participants such as family members:Routinely collected as medical records
Q11. Is there a limit on the number of studies that can be based on this set of patients?
If YES, please give details
Q12a. Please give information on the format and availability of data stored in a database (1)Data summarised in database
Q12a. Please give information on the format and availability of data stored in a database (2)
Q12a. Please give information on the format and availability of data stored in a database (3)
Q12a. Please give information on the format and availability of data stored in a database (4)
Q12a. Please give information on the format and availability of data stored in a database (5)
Please specify language used
Q12b. Please give information on how data is held as individual records (1)Data is held as individual records
Q12b. Please give information on how data is held as individual records (2)
Q12b. Please give information on how data is held as individual records (3)Data held on computer based records
Q12b. Please give information on how data is held as individual records (4)
Please specify language used
Q13a. Is data available to other groups?
Q13b. If data is available to other groups what is the access policy/mechanisms for access?Apply to PI or co-ordinator at resource|Access Committee mechanism|Other access mechanism|Local/ regional access|National access|International access|Access for pilot studies permitted|Access restricted to peer-reviewed work
Q14. What data sharing policy is specified as a condition of use?No requirement to make data publicly available
Q15a. Are tissues/samples/DNA available to other groups?
Q15b. i) If yes, please describe below:
Q15b. ii) In what form are tissues/samples/DNA supplied?
Q15b. iii) Is the access policy/mechanism for obtaining samples the same as that for obtaining data (Q13b above)?
Q16a. Is information on biological characteristics available to other groups?
Q16b. If yes, is the access policy/mechanism for obtaining samples the same as that for obtaining data (Q13b above)?
Types: Disease Registers
Member States: France
Diseases: Neurodegenerative disease in general
Years: 2016
Database Categories: N/A
Database Tags: N/A
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