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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15+
SponsorUniversity Hospital, Angers

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 increase morbidity and decrease quality of life, or even increase the risk of early mortality.

In France, the LOG-AFTER software was developed in 2017 by university hospital of Angers and Epiconcept (approved health data host). The main differences with the European procedure concern radiotherapy information, the link with the General practitioner (GP), and the possible addition of information and/or access to therapeutic education in a video format. Indeed, there is the possibility of creating an GP account allowing to receive notifications concerning the follow-up of his patient to be scheduled, to have access to his file summary and his personalized follow-up plan, various information and blank prescription models. LOG-I is a study of the impact of the LOG-AFTER software for the "patient/GP" couple on adherence to follow-up recommendations. LOG-I is interested in all former patients with at least 3 recommendations in their personalized follow-up plan, taking into account the specific population of patients cured of a brain tumor.

Eligibility criteria

Qualifiers

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 consent (or their parents if the patient is a minor, or a third party if necessary)

Disqualifiers

Patient who has relapsed or developed a second cancer with a post-treatment delay < 5 years

Patient not covered by a health insurance

Patient subject to a legal protection measure, patient deprived of liberty by judicial or administrative decision, patient subject to psychiatric care under duress

Trial design

Treatments tested in this trial

  • Use of the Log-AFTER software

Treatment groups

320 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University Hospital, Angers

Lead sponsor

National Cancer Institute, France

Collaborator