About this trial
The goals of this study is to establish the prevalence of severe forms of FCR in the oncology hospital setting, which will require a specific psychotherapeutic response. Two cancer sites are targeted: breast and pulmonary cancers. Secondary objectives include: 1) Determining threshold scores for the FCRI's 9-item severity scale for each type of cancer; 3) To identify a simple item from the FCRI for early detection of FCR in everyday clinical practice, especially using a digital format.
Eligibility criteria
Qualifiers
Aged 18 or over
Clinical or pathological diagnosis of primary or recurrence of a localized/loco-regional or metastatic breast cancer, or a stage 1 or 2, or stage 3 or 4 lung cancer; or a breast or lung cancer metastatic progression
Three months after completing treatment or three months after the start of a first treatment line for metastatic progression
Able to comply with the scheduled assessment and interviews
Disqualifiers
Participating in another patient-reported outcome study interfering with the present study
Any social, medical or psychological condition hindering questionnaire completion
Being deprived of personal liberty or under guardianship
Trial design
Treatments tested in this trial
- Not listed