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Swiss Childhood Cancer Survivor Study (SCCSS)
Swiss Childhood Cancer Survivor Study logo
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Sample details

SCCSS investigates the long-term health and quality of life of childhood cancer survivors in Switzerland. Participants were recruited from the Swiss Childhood Cancer Registry, which includes individuals diagnosed with cancer before the age of 20 who survived at least five years post-diagnosis. The cohort comprises over 2,700 participants and encompasses a wide range of demographics representative of childhood cancer survivors in Switzerland. Follow-ups are conducted regularly throughout the participants’ lives to monitor their long-term health outcomes and quality of life changes.

Study design
Cohort

Number of participants at first data collection

2,738 (participants)

Recruitment is ongoing

Age at first data collection

Varied (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adolescents
Children and young people
Patients and clinical populations
Pediatric cancer patients
Dataset details

Country

Switzerland

Year of first data collection

2007

Primary Institutions

University of Bern (Universität Bern)

Links

swiss-ccss.ch/en/survey/

Profile paper DOI

doi.org/10.1093/ije/dyr142

Funders

Ambizione - Schweizerischer Nationalfonds

Childhood Cancer Switzerland (Kinderkrebs Schweiz)

European Union (EU)

Swiss Cancer League

Swiss Cancer Research (Krebsforschung Schweiz)

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

Engagement

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

    Biological samples/biospecimens
    Cancer
    Childhood cancer
    Diet and nutrition
    Education
    Lifestyle
    Quality of life
    Work and employment
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