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United Kingdom Research study into Ethnicity And COVID-19 outcomes in Healthcare workers (UK-REACH)
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Sample details

UK-REACH is a prospective cohort investigating the impact of the COVID-19 pandemic on healthcare workers (HCWs) from across the United Kingdom, and focusing on the physical and mental health outcomes of ethnic minority HCWs compared with White HCWs. The cohort included nearly 18,000 HCWs and ancillary workers within healthcare settings, aged 16–89 years, who were recruited from across the United Kingdom, between December 2020 and February 2021. After the baseline survey, participants were followed up every ~6 months until 2025, and data from linked healthcare records will be collected for up to 25 years.

Study design
Cohort - occupational, Cohort

Number of participants at first data collection

17,891 (participants)

Age at first data collection

16 - 89 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Ethnically diverse populations
Healthcare workers
Under-represented groups
Dataset details
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Countries

England, Northern Ireland, Scotland, United Kingdom of Great Britain and Northern Ireland, Wales

Year of first data collection

2020

Primary Institutions

University of Leicester (Academic, United Kingdom)

Links

uk-reach.org/

doi.org/10.1192/bjo.2023.520

Profile paper DOI

doi.org/10.1093/ije/dyac171

Funders

Health Data Research UK (HDRUK) (Research council, United Kingdom)

Medical Research Council (MRC) (Research council, United Kingdom)

NIHR Applied Research Collaboration East Midlands and Leicester NIHR BRC (Research council, United Kingdom)

National Institute for Health and Care Research (NIHR) (Government, United Kingdom)

Ongoing?
Yes

Data types collected

mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Activity log (e.g. food, sleep, exercise)
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Secondary data
  • Self-completed questionnaire – online
Qualitative data collection
  • Interviews or focus groups
Neuroimaging data collection
  • None
Linked or secondary data
  • Healthcare data
Features

Engagement

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

    Biological samples/biospecimens
    Burnout
    COVID-19
    Discrimination
    Health and wellbeing
    Mental health outcomes
    Occupational health and wellbeing
    Pandemic-related stressors
    Vaccinations
    Work and employment
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