Date of filling in this questionnaire or last update: 14/07/2020
1. IDENTIFICATION & BASIC DESCRIPTION
Cohort name
  UK Biobank
Country
 

  • United Kingdom

Please provide any other information on the cohort location/s if needed
  National survey, England and Wales
Name
  Rory Collins
Institution
  University of Oxford
Email
  rory.collins@ndph.ox.ac.uk
Website
 

  • https://www.ukbiobank.ac.uk/

Name of committee
  Multiple
Or provide website
 

  • https://www.ukbiobank.ac.uk/key-documents/

Data access policy (briefly describe)
  http://www.ukbiobank.ac.uk/wp-content/uploads/2012/09/Access-Procedures-2011.pdf
Upload files
 

Main aim of cohort, please briefly describe the main objectives of the cohort
  This is a general population all-purpose cohort of adults, which includes some occupational data.
Study design (please select as many as appropriate)
 

  • Prospective cohort

Source population (please select as many as appropriate)
 

  • General population: National

Comparators (please select as many as appropriate)
 

  • Internal study population

Enrollment
  Completed
Age range at entry (main cohort)
 

Minimum Maximum Mean
40 69 55

Men at enrollment
  250,000
Women at enrollment
  250,000
Children (<18 years) at enrollment
  0
Men at last follow-up
  250,000
Women at last follow-up
  250,000
Participation rate at enrollment (if known)
  5
Comments
  Access is open to all - apply through through the website - there is no need to contact the Principal Investigator
2. OUTCOME FOLLOW-UP
Type of data for outcome follow-up (please select as many as appropriate)
 

  • Active (contact with participants)
  • Death certificate
  • Disease incidence records
  • Hospital / physician diagnoses

Active (contact with participants) (specify)
 

  • Only for special surveys

Death certificate (specify)
 

  • Routine linkage

Disease incidence records (specify)
 

  • Routine linkage, e.g. to cancer registries

Hospital / Physician diagnoses (specify)
 

  • Linkage with hospital admissions

First follow-up period (provide year)
  2006
Last follow-up period (provide year)
  ongoing
Number of follow-ups after baseline (provide number)
  500,000
Participation at last follow-up (if known)
  100
Comments
  Most follow-up is routine record linkage and is therefore close to 100%
3. OCCUPATIONAL EXPOSURES
Source of exposure data collected (please select as many as appropriate)
 

  • Questionnaire, Personal (Self-reporting or interview)
  • Questionnaire, Personal (Occupational/industry modules)

Occupational history/time frame
  Lifetime
Occupational coding performed
  No
4. OUTCOMES EVALUATED
Baseline - type of outcome data collected (select more than one if applicable)
 

  • Biomarker (specify)
  • Clinical/functional evaluation, e.g. spirometry, ECGs (specify)
  • Death certificates
  • Registry-based

Specify: Clinical/functional evaluation, e.g. spirometry, ECGs
  Many
Specify: Biomarker
  Many
Registry-based
 

  • Cancer incidence

Follow-up - type of outcome data collected (select more than one if applicable)
 

  • Death certificates
  • Medical records

Outcome type (please select as many as appropriate)
 

  • Mortality
  • Morbidity

Other health related outcomes
 

  • Biomarkers

5. BIOLOGICAL SAMPLES & ANALYSIS
Biological samples collected
 

  • Blood

Biological processing
 

  • DNA

6. Other Information
Possibility for linkage to data registries/data enrichment via data linkage
 

  • Cancer incidence
  • Hospital discharge

Please describe plans that are funded or most likely to be funded
  The cohort is gathering more information all of the time, particularly with record linkage