decrease of side effect of chemotherapy by continuous care model

Not Applicable

• Conditions: Breast cancer.; Malignant neoplasm of Breast; C50.0, C50

• Registration Number: IRCT2013070613802N2
• Lead Sponsor: Ahvaz Jundishapor University Of Medical Sceinces

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 74

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

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.