The aim of this study is to test whether a short educational intervention about emotional skills can improve survivor cancer patient emotional skills and quality of life. Half of participants will follow the educational intervention about emotional skills, while the other half will practice relaxation followed by a non-directive talking group. The educational intervention should give better results on patient emotional skills and quality of life than the control group.
After the end of treatments, cancer patients face a difficult time because it is expected that they return to normal, but at the same time they still have to struggle with the aftermath of cancer and fear of recurrence. This is why there is room in this period for an intervention designed to help patients to cope with their emotions. . Patient emotional skills are patient abilities to identify, express and manage their emotions for the best possible psychological adjustment. In general population, emotional skills have been shown to be highly related to a better quality of life. In this randomized controlled study, bronchopulmonary and oesogastric cancer patients between 6 months and 2 years after the end of treatments will undergo either the emotional skills intervention (intervention group) or the relaxation group (control group).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
23
2-hour 3 group sessions
2-hour 3 group sessions
Hôpital Calmette,CHU
Lille, France
Change in patient emotional skills from baseline to 15 days after intervention
Variation of patient-reported Short Profile of Emotional Competence (S-PEC)questionnaire score from baseline to 15 days after the intervention (between 1 and 3 months)
Time frame: Baseline and 15 days after the end of the intervention
Patient emotional skills long term
Variation of patient-reported PEC (Profile of Emotional Competence) questionnaire score
Time frame: T1 (15 days after the end of the intervention) and T2 (2 months after T1) : 2 months
Quality of life by Medical Outcome Study Health Survey Short Form-36 (MOS SF-36)
Patient-reported health-related quality of life using the Medical Outcome Study Health Survey Short Form-36 (MOS SF-36)
Time frame: Baseline (T0), 15 days after the end of the intervention (T1), 2 months
Patient participation in workshops
The percentage of patients who have attended the 3 group sessions
Time frame: Between 2 weeks and 2 months
Patient adherence to exercises to do at home between sessions
The percentage of patients who have performed the suggested exercises at home between sessions
Time frame: Between 2 weeks and 2 months
Patient satisfaction
Patient-reported satisfaction regarding the intervention using and ad hoc questionnaire
Time frame: T1 (15 days after the end of the intervention) and T2 (2 months after T1)
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