Breast Cancer. Malignant neoplasm of breast
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Undergoing chemotherapy, including taxane agents (such as docetaxel and paclitaxel) Elderly over 65 years old Reported a score greater than five on a numerical rating scale for pain symptoms in the past week (indicating more severe than average pain) Possibility to participate in the plan for four weeks The ability to communicate and the absence of speech and hearing problems
Exclusion criteria
Exclusion criteria: 12 months or more have passed since the end of their chemotherapy treatment They had skin inflammation, or used hearing aids, or had piercings or holes in the intervention sites During the study period, they are under chemotherapy or radiotherapy Ear acupressure experience within 3 months before participating in the study Metastatic cancer status Have psychiatric diseases or other diseases that can affect this study (Alzheimer's, delirium, rheumatoid arthritis)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Chemotherapy-induced peripheral neuropathy score in Chemotherapy-Induced Peripheral Neuropathy-20 (CIPN-20), health-related quality of life score in Functional Assessment of Cancer Therapy-General (FACT-G), pain score in The Numeric Rating Scale. Timepoint: Questionnaires are given to the participants before the intervention, immediately after the end of the intervention and two weeks after the end of the intervention, or they are completed with an interview. Method of measurement: Chemotherapy-Induced Peripheral Neuropathy-20 questionnaires (CIPN-20), Functional Assessment of Cancer Therapy-General questionnaires (FACT-G), The Numeric Rating Scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Kerman University of Medical Sciences