Breast cancer. Malignant neoplasm of Breast
Conditions
Interventions
Intervention 1: intervention group: Continuous Care Model (Including orientation, sensitization, monitoring and evaluation) in the intervention group and measurements related to sleep, fatigue, pain,n
Prevention
intervention group: Continuous Care Model (Including orientation, sensitization, monitoring and evaluation) in the intervention group and measurements related to sleep, fatigue, pain,nasea and body im
control group: in the control group the patients will be received only routine cares
Sponsors
Ahvaz Jundishapor University Of Medical Sceinces
Eligibility
Sex/Gender
Female
Age
25 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Being aware of the time and place; The lack of a clear and well-known sleep disorders, pain, fatigue, nausea and vomiting in the patient's medical history is mentioned; Lack of mental and brain diseases in the patient's medical history is mentioned (Thease has the effect of variables);The absence of severe dyspnea in patients; Not receiving the sleep-disrupting drugs such as diuretic drugs, antidepressants, and amphetamines and inotropes at night; Age 65-25 years; known Persian language; Patients who have a minimum of one and a maximum of 5 sessions of chemotherapy; Patients with stage II, III and IV disease. Exclusion criteria: Get an anesthetic and narcotic drugs during the study; Patient's unwillingness to continue participation in the study; Acute complications during the study; Get the sleep-disrupting drugs such as diuretic drugs, antidepressants, and amphetamines and inotropes at night; Need CPR during the intervention
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep quality. Timepoint: beginning of study, two months after intervention. Method of measurement: pittsburgh sleep quality Questionnaire.;Pain. Timepoint: beginning of study, two months after intervention. Method of measurement: pain assessment questionnaire.;Fatigue. Timepoint: beginning of study, two months after intervention. Method of measurement: fatigue summarized check list.;Nasea. Timepoint: beginning of study, two months after intervention. Method of measurement: nasea assessment questionnaire.;Body image. Timepoint: beginning of study, two months after intervention. Method of measurement: Body image scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahsa Imanian
Ahvaz Jundishapor University Of Medical Sceinces
Outcome results
None listed