LOG-I - Impact Study of LOG-AFTER Software on Long-term Monitoring of Former Patients (LOG-I - LOG-Impact Study)

Recruiting N/A Interventional Study
Pediatric Cancer Cancer Survivor Hemato-oncologic Patients
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
15 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
320 (estimated)
Sponsor
University Hospital, Angers · Government
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About This Trial
Childhood cancer survivors represent a high-risk population that requires risk-based follow-up. Follow-up recommendations have been harmonized. Education and information practices regarding follow-up recommendations should be personalized, to ensure understanding by all survivors, including those with neurocognitive disorders. Individualized follow-up is necessary to detect complications that may …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Previously treated for cancer or malignant hematological pathology before the age of 25 * Without residual disease or with a stable disease without treatment for 5 years or more * Owning a computer, smartphone or equivalent I-Pad/tablet with internet access * Having signed the…
Contacts

Sandra MERZEAU

(+33)2 41 35 59 70

samerzeau@chu-angers.fr

CONTACT

Pascal VEILLON

(+33)2 41 35 49 59

paveillon@chu-angers.fr

CONTACT