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St. Jude Lifetime Cohort Study (SJLIFE)
St. Jude Lifetime Cohort Study logo
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Sample details

SJLIFE is a retrospective cohort that was established to follow-up the health of adults treated for cancer during childhood and adolescence. Eligibility criteria for participation in SJLIFE initially includes diagnosis of pediatric cancer treated or followed at St. Jude Children's Research Hospital (SJCRH), attained age of 18 years or older, and survival of 10 or more years from diagnosis. In 2015, eligibility criteria were expanded to include 5-year survivors of any age up to June 30, 2012. Whereas SJLIFE does not specify age at cancer diagnosis, SJCRH generally restricts acceptance to children < 25 years of age at the time of cancer diagnosis. The most common forms of pediatric cancer include leukaemia, lymphoma, and central nervous system malignancy. SJLIFE participants (both in the original and expanded cohorts) are invited to return to SJCRH at least once every 5 years.

Study design
Cohort - clinical, Cohort - open

Number of participants at first data collection

5,223 (participants)

Recruitment is ongoing

Age at first data collection

≥ 18 years (participants)

Varied (participants recruited after 2012)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Cancer patients
Patients and clinical populations
Pediatric cancer patients
Dataset details

Country

United States of America

Year of first data collection

1962 (hospital data)

2007 (SJLIFE inception)

Primary Institutions

St. Jude Children's Research Hospital

Links

sjlife.stjude.org/

Profile paper DOI

doi.org/10.1093/ije/dyaa203

Funders

American Lebanese Syrian Associated Charities

National Cancer Institute (NCI)

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Interview – phone
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • 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

  • Community engagement
  • Participant or community advisory groups
  • Keywords

    Biological samples/biospecimens
    Cancer
    Childhood cancer
    Neurocognition
    Neuromuscular function
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