Effects of a Neuroscience-based Technique on Cancer Patients Announced of a Palliative Disease Progression and Partners

Procedure for patients and partners: Patients will be informed about the study by their treating oncologist at the end of the appointment, when they will be informed about the metastatic incurable progression of their disease (announcement visit). Oncologists will provide the patients a written description of the study, presenting the information previously orally provided by them, together with the consent form, to fill in. Signed informed consent will be sent back by post-mail if necessary (if participants ask for a time to think), using a pre-stamped envelope. Due to the objective to prevent distress, recruitment to the study and random assignment of the intervention need to be performed within the 7 days following this announcement visit, after making sure the patient is eligible for the study according to the inclusion and exclusion criteria. Early after the announcement visit and consent collection, the clinical psychologist will call the patient before randomization in order to assess patients' level of stress from 1 (no stress) to 10 (maximal stress). Patients with a level higher or equal than 4 will be randomized in the study. For the patients with a stress level below or equal than 3, only background information will be collected in the study. These patients will receive the standard care. Patients and their spouse will be randomly assigned together (i.e., if the spouse participates, he/she will be allocated to the same treatment arm as the patient) to receive the MSI + VB (experimental group) or to receive the supportive listening and attention (usual care serving as control condition), using an online centralized randomization program. Randomization will be implemented after the receipt of the consent form and balanced by (1) cancer type (bladder, prostate, kidney, colorectal cancer, sarcoma), (2) gender, as these two variables are identified as risk factors of PTSD (for cancer type) and as impacting the MSI effects (for gender) in the literature, and (3) the presence of the spouse during the announcement visit (yes/no), using a dynamic allocation program (minimization with a random factor set at 0.8). For reasons of feasibility, no pre-screening aiming at including patients with a high risk of distress and potentially with high risk for developing PTSD will be realized. However, during the first telephone session, the psychologist will assess patients' level of stress using a 10-point likert scale, similar to a past study, before and after the MSI + VB intervention or the support and attention control session. This scale includes asking patients on a scale from 1 (no stress) to 10 (maximal stress) their level The treatment consists of a single telephone session conducted by a trained therapist maximum 10 days after receiving the announcement of the incurable disease progression. This is done in order to prevent PTSD, as was already done when the MSI treatment was developed in traffic accident survivors (Gidron et al., 2001, 2007). The same trained therapist will provide the MSI + VB intervention to the experimental group and give support and attention to the control group, in order to control for therapist's effects. This telephone session will be followed by 3 follow-up telephone assessments (a week, a month and 3 months after the previous telephone session), for collecting data by a research assistant who will not know in which group the participants are. All the sessions and interviews of the patient and his/her spouse (for treatments and for follow-up measures) will be conducted separately, and the information will remain confidential between the patient and the spouse. Each of these telephone calls will be conducted from the participating center, in order contact details of the participants remain inside the medical center to ensure the confidentiality of the data. Experimental intervention. In the experimental group, participants will perform vagal breathing (VB), followed by the MSI, followed again by VB. The VB component will guide participants how to perform deep slow vagal breathing by inhaling and counting 1-5, holding their breath and counting 1-2, and exhaling and counting 1-5, during 2-5 minutes. The MSI component will teach participants to chronologically organize the segments of their memory of the incurable diagnosis, to verbally label feelings or somatic sensations they had at that moment, and to provide causal links between the event's segments and causality to their feelings and sensations, following the protocol of Gidron et al. (2001). In the MSI part, the patient will talk, and the therapist will note the different event parts and their real timing. Each time the patient says a feeling or sensation, the therapist will ask to verbally elaborate and provide the cause of these feelings and sensations. Then, the therapist will retell the story in a chronological manner, with verbal titles and causes for feelings and sensations. Finally, the patient will be asked to retell the story in this structured manner, after being explained how to do so. patients in the MSI + VB group will be encouraged to perform it daily, for 5-10min, and especially before going to bed, to reduce any sleeping arousal associated with PTSD symptoms Control. Participants in the control group will receive support and attention (usual care) and will be invited to recall announcement of the incurable disease progression. More precisely, they will be invited to express their associated thoughts and feelings, being free to talk about their experience, and the psychologist will react with empathy and support. At Baseline for both arms, i.e., at the beginning of the telephone interview where the trained therapist will call the participants, the therapist will collect background information including age, gender, years of education, self-reported length of couple relationship and psychotropic medication (anxiolytic, antidepressant) in order to control the association between PTSD symptoms and anxiety and/or depressive disorder. 1. PTSD symptoms will be assessed by the post-traumatic checklist for DSM 5 (PCL-5; Weathers et al., 2013, French translation and validation by Ashbaugh et al., 2016). 2. Emotional regulation will be assessed by the BACQ scale (Finset et al., 2002). 3. Quality of life will be assessed by the EuroQol-5D scale (EQ-5D 3L) In both groups, the trained therapist will also evaluate the degree of "natural" structuring regarding the way in which the patients/partners talk about the announcement visit. More precisely, the trained therapist will rate both groups on their level of chronological organization of their story from 1 = totally disorganized; 2 = a bit organized; 3 = chronologically very organized (in the MSI + VB group: before and after the MSI training; in the control group: at the first time they recall their story) Afterwards, three follows-ups will be conducted by telephone: 1 week, 1 month and 3 months after the first intervention or control phone session.A research assistant blind to group assignments will collect the same self-reported measures initially collected by telephone at the first phone meeting. In sum, levels of PTSD symptoms and quality of life will be assessed at each time (initial phone meeting, 1 week, 1 month and 3 months). However, emotional regulation will be assessed at the first phone meeting and at one month only, in order to reduce patients' burden. Patients and partners will also be asked if they have talked about the event, to recall how and how often they have spoken about the event since the last phone call. For all the groups, medical information including type and stage of cancer and type of cancer treatments will be collected at baseline by the medical staff (as summarized in the table below). Levels of albumin and levels of C-reactive protein (CRP, reflecting inflammation) will also be obtained at baseline, 1 month and 3 months when patients will come in any case to the hospital for their medical appointments (no medical appointment is anticipated at 1 week, hence the absence of CRP and albumin measures at this time). Survival time will be monitored for all patients as well until the final analysis. We will calculate the quality-adjusted life years (QALY) for all patients, to reflect both quantity and quality of survival. This will be done using the length of survival weighted by patients' score on the EQ-5D scale.