About this trial
The goal of this clinal trial is to compare the effectiveness of nurse-led teleconsultation with usual care (intervention group) on psychological distress in patients with primary malignant tumors of the central nervous system between diagnosis and first anti-cancer treatment, versus usual care alone (control group).
Participants will be randomized into two groups :
* group A) intervention: usual care + nurse teleconsultation for psychological support * group B) control: usual care alone
Enrolment = Day0 (D0)
Participants will :
* groups A and B: D0: complete 4 questionnaires (Quality of Life, Screening for Distress, Screening for Anxiety and Depression, Social Support Questionnaire) * Group A : D0+2/4 das : nursing teleconsultation for psychological support * Groups A and B: D0+10days : telephone call to complete the same 4 questionnaires as at inclusion * Group A : D0+15days: semi-directive interview, at home, for voluntary patients.
Eligibility criteria
Qualifiers
aged 18 and over
being treated for a primary malignant tumor of the central nervous system (positive biopsy)
with a Mini-Mental State score greater than 24
not receiving first-line treatment (chemotherapy, targeted radiotherapy, surgery)
Disqualifiers
with a history of psychiatric illness
with recurrent cancer of the cerebral nervous system
having begun first-line treatment (drug therapy, curative surgery, radiotherapy or palliative care)
under guardianship, curatorship or deprived of liberty
Trial design
Treatments tested in this trial
- Teleconsultation for psychological support