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Life and Living in Advanced Age: a Cohort Study in New Zealand (LiLACS NZ)
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Sample details

LiLACS NZ investigates the health, social, cultural, and environmental status and predictors of successful advanced ageing of Māori and non-Māori individuals in advanced age in New Zealand. Participants at baseline included Māori who, in 2010, were aged between 80 and 90 years (born between 1 January, 1920 and 31 December, 1930) and non-Māori who were aged 85 years (born between 1 January and 31 December, 1925). Geographical boundaries of the District Health Boards of the Bay of Plenty and northern part of the Lakes areas were chosen as a stable population base and area of Māori communities. At baseline, the sample included 421 Māori participants and 516 non-Māori participants. The cohorts were followed up yearly and Wave 6 (5-year follow-up) began in 2015.

Study design
Cohort

Number of participants at first data collection

937 (participants)

Age at first data collection

80 - 90 years (participants)

Participant year of birth

1920 - 1930 (participants)

Participant sex
All

Representative sample at baseline?
For Māori participants, sex and age distribution matched the general population; and for non-Māori participants, more men were recruited than expected.

Sample features

Older and elderly people
Racial and ethnic minorities
Dataset details

Country

New Zealand

Year of first data collection

2010

Primary Institutions

Auckland University of Technology

Massey University

University of Auckland

University of Otago (Ōtākou Whakaihu Waka)

Links

fmhs.auckland.ac.nz/en/faculty/lilacs.html

Profile paper DOI

doi.org/10.1093/ije/dyv103

Funders

Auckland Medical Research Foundation

Health Research Board (HRB)

Ministry of Health (Manatū Hauora)

New Zealand Heart Foundation

Ngā Pae o te Māramatanga

Ongoing?
Yes

Data types collected

mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
  • Mortality data
Features

Engagement

  • Patients, service users, lived experience involvement
  • Participant or community advisory groups
  • Community engagement
  • Keywords

    Ageing
    Biological samples/biospecimens
    Diet and nutrition
    Ethnic minorities
    Morbidity and mortality
    Physical health
    Social support

    Consortia and dataset groups

    Towards Understanding Longitudinal International Older People Studies (TULIPS) Consortium
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