Actively Recruiting

Age: 5Years +
All Genders
Healthy Volunteers
NCT03297034

Swiss Childhood Cancer Survivor Study

Led by University of Bern · Updated on 2025-06-03

4076

Participants Needed

1

Research Sites

2243 weeks

Total Duration

On this page

Sponsors

U

University of Bern

Lead Sponsor

S

Swiss Pediatric Oncology Group

Collaborating Sponsor

AI-Summary

What this Trial Is About

The SCCSS is designed to investigate which long-term effects childhood cancer and its treatment have on survivors, and includes those who were under 20 years when they were diagnosed. The SCCSS explores childhood cancer survivors' quality of life, the health care received by childhood cancer survivors during follow-up care, the effects of medication, somatic and psychosocial health issues, how childhood cancer survivors take care of their own health including health behaviors, and also collects demographic details like family background, education and profession. To learn more about these topics, the investigators send questionnaires to childhood or adolescent cancer survivors. The investigators use the results to inform physicians and patients, and to improve treatment of childhood cancer and follow-up.

CONDITIONS

Official Title

Swiss Childhood Cancer Survivor Study

Who Can Participate

Age: 5Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with cancer before age 20 years
  • Survived at least 5 years after cancer diagnosis
  • Swiss resident at time of cancer diagnosis
  • Provided informed consent to participate
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Institute of Social and Preventive Medicine (ISPM), University of Bern

Bern, Switzerland, 3012

Actively Recruiting

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Research Team

C

Claudia E Kuehni, Prof.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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