Chemotherapy-induced nausea and vomiting in women with breast cancer. ???????? ????? ?????
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants have the consent to participate in the study Have organ health in the legs in the reflexology group Have organ health in the eardrum in the auricular therapy group The patient is fully conscious The patient can understand, read, write and speak Persian. The patient is being treated and has received at least one course of chemotherapy The patient is not undergoing other studies or treatments at the same time The diagnosis of breast cancer is made by an oncologist The results of diagnostic tests have been confirmed by an oncologist
Exclusion criteria
Exclusion criteria: The patient does not have the desire to participate in the study The patient has mental problems, blindness, deafness, or a history of psychological issues The patient does not feel nauseous after chemotherapy The patient is undergoing other studies or treatments at the same time The patient is not fully conscious
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Nausea and vomiting score in Rhodes questionnaire INV 2. Timepoint: Before, 6 hours after, 12 hours after, 24 hours after the intervention. Method of measurement: Rhodes Nausea and Vomiting Questionnaire Form 2 (INV-2). | — |
Countries
Iran (Islamic Republic of)
Contacts
Birjand University of Medical Sciences