Effect of discharge planning on quality of life of patients with gastrointestinal cancer

Intervention 1: Intervention group: At the time of admission of patients in the hospital, at the first session, filling out a questionnaire on quality of life in these patients and measuring the BMI will be carried out. Then, the patients will be evaluated by the form of the most common complications of patients under American Cancer Chemo Chemotherapy and then prioritizing the complications. Based on life threatening and post-traumatic training on complications according to the complications noted to the patient and his family on the second day of education in the field of complications according to the complications noted to the patient and his family on the third day of education in the field of complications according to the complications noted to the patient and his family The training time will be 45-60 minutes per session. The third, fifth and fifth days after discharge, according to the priority of the specified complications, will be sent to the patients ‘mobile phone. One month after the first assessment at the time of referral to the hospital, patients’ quality of life was assessed using a questionnaire and body mass index using weight and size Will be done. Intervention 2: Control group: In the control group, on the first day of admission, filling in the quality of life measurement and body mass index in the hospital, then measuring the quality of life and BMI will be done one month after the first assessment.
Primary outcome(s): Quality of life. Timepoint: At the beginning of the study, the month after the study. Method of measurement: The EROTIC core quality of life questionnaire.;Body Mass index. Timepoint: At the beginning of the study, the month after the study. Method of measurement: Digital weight and meter measurement scale.
Study Design: Randomization: Not randomized, Blinding: Not blinded, Placebo: Not used, Assignment: Parallel, Purpose: Education/Guidance.