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Clinical Trial Summary

EFACog is a single-center prospective cohort feasibility study conducted on a single group of patients to study the feasibility of a personalized support program by a nurse conducted over 9 months, using face-to-face and telephone interviews. The objective of this support program is to prevent the occurrence of post-chemotherapy cognitive impairment. After a pre-inclusion visit, patients with no pre-existing cognitive impairment will be included in the study and will receive a 9-month follow-up after the first course of chemotherapy. All follow-up visits (telephone or face-to-face) will be scheduled in conjunction with those taking place in the care setting.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05538000
Study type Interventional
Source Institut de Cancérologie de Lorraine
Contact MERLIN JEAN LOUIS, PharmD, PhD
Phone + 33 3 83 65 60 62
Email jl.merlin@nancy.unicancer.fr
Status Not yet recruiting
Phase N/A
Start date May 2024
Completion date May 2027