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Lifepool
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Sample details

The Lifepool cohort was set up in an attempt to improve the screening, prevention, and management of breast cancer in women living in Australia. Participants were recruited through breast screening programs, which are available to women aged 40 years and over in Australia, with and without a history of breast cancer. Recruitment began in Victoria in 2010 and was expanded nationally from 2015, with over 55,000 participants completing baseline data collection as of February 2024. Recruitment is ongoing and participants are being followed up annually through linked cancer and mortality registries.

Study design
Cohort, Registry

Number of participants at first data collection

55,700 (participants, as of 2024)

Recruitment is ongoing

Age at first data collection

Varied (participants)

Participant year of birth

Varied (participants)

Participant sex
Female

Representative sample at baseline?
No

Sample features

Adults
Middle-aged people
Older and elderly people
Women
Dataset details

Country

Australia

Year of first data collection

2010

Primary Institutions

Peter MacCallum Cancer Centre

Links

lifepool.org/

nbcf.org.au/project-completed/lifepool-is-a-powerful-and-unique-resource-that-will-facilitate-the-development-and-validation-of-new-ideas-for-treatment-and-early-detection-of-breast-cancer/

oup.silverchair-cdn.com/oup/backfile/Content_public/Journal/ije/54/3/10.1093_ije_dyaf044/3/dyaf044_supplementary_data.pdf

petermac.org/research/cohort-studies/lifepool

Profile paper DOI

doi.org/10.1093/ije/dyaf044

Funders

National Breast Cancer Foundation (NBCF)

Peter MacCallum Cancer Centre

Ongoing?
Yes

Data types collected

dataLinkage
Quantitative data collection
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – online
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Biological samples/biospecimens
    Breast cancer
    Cancer
    Cancer registry
    Genetics
    Registry
    Women's health
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