Effects of Acupressure and Aromatherapy on Nausea and Vomiting Severity, Anxiety and Comfort Level
NCT ID: NCT06529458
Last Updated: 2024-08-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
60 participants
INTERVENTIONAL
2024-08-29
2025-08-30
Brief Summary
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It will be conducted on patients diagnosed with breast cancer who are receiving treatment at the Erciyes University Health Application and Research Center Nazende-Nuri Özkaya Oncology Day Treatment Center. A total of 60 patients, 20 patients in control, 20 patients in Intervention 1 and 20 patients in Intervention 2 who meet the inclusion criteria, will be included in the sample according to the block randomization list created in the computer environment. Attention will be paid to ensure that the patients have similar characteristics such as being diagnosed with breast cancer, receiving chemotherapy for the first time, using the same chemotherapy drugs and the same antiemetic drugs (Adriablastin, Cyclophosphamide, Kytril), gender and age. No application will be made to the control group.
Data; Data will be collected using the Informed Consent Form, Patient Introduction Form, Visual Analog Scale (VAS), Rhodes Nausea, Vomiting and Retching Index (INVR), General Comfort Scale-Short Form, State-Trait Anxiety Inventory (STAI), Patient Monitoring Schedule-Researcher Form, Acupressure Application Protocol, Acupressure and Aromatherapy Application Protocol.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Intervention 1 Group
The researcher will apply pressure to the P6 acupressure point on both wrists for approximately 5 minutes at the same time as chemotherapy. He will also have the patient or a relative repeat the method and do it at home three times a day before meals for 5 days.
Intervention 1 Group
The researcher will apply pressure to the P6 acupressure point on both wrists for approximately 5 minutes at the same time as chemotherapy. He will also have the patient or a relative repeat the method and do it at home three times a day before meals for 5 days.
Intervention 2 Group
The researcher will apply drops of ginger oil to the P6 acupressure point on both wrists for approximately 5 minutes at the same time as chemotherapy, using circular motions. At the same time, the researcher will have the patient or a relative repeat the method and apply it at home three times a day before meals for 5 days.
Intervention 2 Group
The researcher will apply drops of ginger oil to the P6 acupressure point on both wrists for approximately 5 minutes at the same time as chemotherapy, using circular motions. At the same time, the researcher will have the patient or a relative repeat the method and apply it at home three times a day before meals for 5 days.
Control Group
No interference will be made
Control Group
No interference will be made
Interventions
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Intervention 1 Group
The researcher will apply pressure to the P6 acupressure point on both wrists for approximately 5 minutes at the same time as chemotherapy. He will also have the patient or a relative repeat the method and do it at home three times a day before meals for 5 days.
Intervention 2 Group
The researcher will apply drops of ginger oil to the P6 acupressure point on both wrists for approximately 5 minutes at the same time as chemotherapy, using circular motions. At the same time, the researcher will have the patient or a relative repeat the method and apply it at home three times a day before meals for 5 days.
Control Group
No interference will be made
Eligibility Criteria
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Inclusion Criteria
* Understand and communicate in Turkish,
* Those who are diagnosed with breast cancer and receive their first course of chemotherapy,
* Those who are receiving platinum group chemotherapeutic agents (Adriablastin, Cyclophosphamide) that have a high emotogenic effect,
* Those who are not pregnant and not planning to be pregnant,
* Those whose disease stage is at most stage III,
* Those who do not have any psychiatric disorders,
* Those who do not have wounds, lesions, etc. in the areas where acupressure will be applied
Exclusion Criteria
* Those who are allergic to ginger or are bothered by its smell,
* Those who receive simultaneous radiotherapy,
* Those who use other complementary and integrated treatment practices during the treatment process will be excluded from the study.
18 Years
ALL
No
Sponsors
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Setenay Batır
OTHER_GOV
Responsible Party
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Setenay Batır
Lecturer
Locations
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Setenay Batır
Kayseri, , Turkey (Türkiye)
Countries
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Central Contacts
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Pınar Tekinsoy Kartın
Role: CONTACT
Facility Contacts
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Pınar Tekinsoy Kartın
Role: primary
References
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Genc F, Tan M. The effect of acupressure application on chemotherapy-induced nausea, vomiting, and anxiety in patients with breast cancer. Palliat Support Care. 2015 Apr;13(2):275-84. doi: 10.1017/S1478951514000248. Epub 2014 Apr 30.
Other Identifiers
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Acupress and aromatherapy
Identifier Type: -
Identifier Source: org_study_id
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