Phase
Condition
Vomiting
Lactose Intolerance
Breast Cancer
Treatment
Chewing Gum Group (Group 2)
Oral Cryotherapy Group (Group 1)
Clinical Study ID
Ages 18-65 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Women aged between 18 and 65 years,
Scheduled to receive adjuvant chemotherapy for the first time,
Receiving the AC protocol as their chemotherapy regimen,
Receiving chemotherapy doses classified as moderately emetogenic (according to theInternational Society of Supportive Care in Cancer Guidelines),
Not having received radiotherapy prior to adjuvant chemotherapy,
Without chronic diseases (coronary artery disease, chronic kidney disease, ordiabetes mellitus),
Not having used any non-pharmacological method for nausea and vomiting,
Diagnosed with breast cancer for the first time,
Without metastasis,
Without thrombocytopenia,
At an early stage,
Aware of their diagnosis,
Open to communication and cooperation,
Literate,
Not receiving psychiatric and/or depression treatment,
Not in the terminal stage,
Willing and volunteering to participate in the study.
Exclusion
Exclusion Criteria:
Illiterate,
Over 65 years of age,
Using anxiolytic or antidepressant medications,
Having chronic diseases (gastrointestinal obstruction/disease, hepatitis, coronaryartery disease, chronic kidney disease, or diabetes mellitus),
Having metastasis,
Having received radiotherapy prior to adjuvant chemotherapy,
Not willing to participate in the study.
Study Design
Study Description
Connect with a study center
Hacettepe University
Ankara 323786, Adnan Saygun 06100
Turkey (Türkiye)Site Not Available

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