Table 1.

Phases of the clinical project and moments of administration of the research project

Clinical phases	Phases of the Fil-Rouge project		Research steps
	TAU group	FRIPOS group
Preliminary phase	-	-	Administration of informed consent Randomization process
I Diagnostic phase	Discussion with the medical staff (radiotherapist/breast specialist)	Integrated session with medical staff (breast radiologist/psycho-oncologist) Individual discussion with the psycho-oncologist for the management of experiences related to the diagnosis
II Pre-surgery phase	Discussion with medical staff (radiotherapist/breast specialist/surgeon)	Integrated session with medical staff (breast radiologist/surgeon/psycho-oncologist) Individual discussion with the psycho-oncologist for the emotional management of the pre-surgery experience	T0 Administration of the socio-demographic questionnaire Administration of SCL-90-R
III Initial phase of treatment	Discussion with medical staff (oncologist/radiotherapist)	Integrated session with medical staff (surgeon/radiotherapist/psycho-oncologist) Individual discussion with the psycho-oncologist for the emotional management of the experience related to the treatment phase	T1 Administration of EORTC QLQ-C30 Administration of EORTC QLQ-BR23
IV Follow-up during the treatment	Discussion with medical staff (oncologist/radiotherapist)	Integrated session with medical staff (surgeon/radiotherapist/psycho-oncologist) Individual discussion with the psycho-oncologist for the emotional management of the experience related to the treatment phase	T2 Administration of SCL-90-R Administration of EORTC QLQ-C30 Administration of EORTC QLQ-BR23