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.
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