Investigation of the Effect of Oral Care With Coconut Oil on the Degree of Oral Mucositis in Pediatric Oncology Patients
Oral Mucositis
About this trial
This is an interventional health services research trial for Oral Mucositis focused on measuring oral mucositis, child, cancer, Oral care, Nursing, coconut oil
Eligibility Criteria
Inclusion Criteria: Being between 7-18 years old, Having been diagnosed with cancer, Receiving chemotherapy at least every 21 or 28 days, Willingness and volunteering to participate in the study, Being able to speak Turkish and express himself Exclusion Criteria: Not being healthy inside the mouth before chemotherapy, Being in terminal period, Being receiving radiotherapy Not willing or voluntarily to participate in the study, Not knowing Turkish.
Sites / Locations
- Başakşehir Çam and Sakura City Hospital
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
No Intervention: Control group
Experimental: Experimental Group
Consent is obtained with an informed consent form. Patient identification form is filled. The patient's mouth is evaluated using the World Health Organization Mucositis Classification and the International Pediatric Mucositis Rating Scale (ChIMES) before receiving chemotherapy. According to the World Health Organization Mucositis Classification, the frequency of oral care is decided. The patient's mouth is evaluated using the World Health Organization Mucositis Classification and the International Child Mucositis Evaluation Scale (ChIMES) on days 0, 7, and 14, and after each assessment, the frequency of oral care is determined and applied for 21 days. The final assessment is made on Day 21. The care given according to the frequency of oral care determined according to the score obtained by the patient in the World Health Organization Mucositis Classification is recorded on the "Basic Oral Care Protocol Follow-up Chart".
Unlike the control group, the experimental group is rinsed with 5 ml of coconut 4 times a day.