Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:20 AM
Ignite Modification Date:
2025-12-25 @ 3:20 AM
NCT ID:
NCT06781905
Eligibility Criteria:
Inclusion Criteria:
* Adult patients aged 18 years or older, fluent in French
* Currently treated with anti-ITK-ALK/ROS1 for ALK/ROS1-positive lung cancer
* Identified by the prescribing physician as having complaints with or without associated neurocognitive and/or neuropsychiatric disorders related to the treatment.
Exclusion Criteria:
* History of neurocognitive and/or neuropsychiatric disorders prior to initiation of anti-ITK-ALK/ROS1 targeted therapy, excluding disorders associated with anti-ITK-ALK/ROS1 or other systemic anticancer treatments
* Patients with uncontrolled brain metastases or carcinomatous meningitis (requiring symptomatic treatment with corticosteroids progressive or symptomatic)
* Patients who do not have sufficient proficiency in French to complete questionnaires and/or participate in semi-structured interviews
* Severe, progressive or unstable medical conditions that may interfere with the evaluation variables (uncontrolled epilepsy, acute psychiatric or psychotic disorders, visual hallucinations, acute infection).
* Consumption of toxic substances that may affect cognitive performance
* Deafness or blindness that may compromise participant evaluation or participation in tasks and scales
* Patients who refuse to participate in the study or are unable to express thein non-opposition to participating in the study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06781905
Study Brief:
Protocol Section:
NCT06781905