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International Registry for Men with Advanced Prostate Cancer (IRONMAN)
International Registry for Men with Advanced Prostate Cancer logo
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Sample details

IRONMAN is an international study focused on improving outcomes for men with advanced prostate cancer. Study participants had a diagnosis of prostate cancer, were at least 21 years old, and were recruited from over 100 sites in 16 countries, namely Australia, Barbados, Brazil, Canada, Ireland, Jamaica, Kenya, Nigeria, Norway, Spain, South Africa, Sweden, Switzerland, United Kingdom, and United States of America. As of 2023, over 3,000 participants have completed the baseline assessment. Follow-up assessments are conducted every three months for the first two years, and then every six months thereafter for at least 5 years.

Study design
Registry

Number of participants at first data collection

3,092 (participants as of 2023)

Recruitment is ongoing

Age at first data collection

≥ 21 years (participants)

Participant year of birth

Varied (participants)

Participant sex
Male

Representative sample at baseline?
No

Sample features

Cancer patients
Ethnically diverse populations
Veterans
Dataset details
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Countries

Australia, Barbados, Brazil, Canada, Ireland

Year of first data collection

2017

Primary Institutions

Movember Foundation

Prostate Cancer Clinical Trials Consortium (PCCTC)

Yale University

Links

ironmanregistry.org/

clinicaltrials.gov/study/NCT03151629

doi.org/10.1200/go.20.00571

Profile paper DOI

doi.org/10.1200/GO.22.00154

Funders

Janssen Pharmaceutical Research & Development LLC

Amgen Inc.

Astellas Pharma Inc. (アステラス製薬株式会社)

AstraZeneca

Bayer UK

Ongoing?
Yes

Data types collected

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

Engagement

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

    Men's health
    Multi-site
    Pain
    Prostate cancer
    Quality of life
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