Phase
Condition
Neurologic Disorders
Treatment
Experimental- Heat application
Experimental-Cold application
Clinical Study ID
Ages 18-75 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Women with stage III-IV breast cancer receiving 4-7 cycles of taxane-based chemotherapy,
Patients with chemotherapy-induced neuropathy symptoms,
Residents of Ankara,
Over 18 years older,
No history of nerve damage or psychiatric illness,
No central nervous system metastasis or disease,
No irritation or ulceration in the skin area where the application will be made,
No history of deep vein thrombosis,
Not using anticoagulant medication,
Able to speak, understand, and read/write in Turkish,
Patients who consent to participate in the study will be included.
Exclusion Criteria
Patients with a history of nerve damage or psychiatric illness,
Ulcers or irritation in the area where the application will be made,
Patients with peripheral neuropathy developed due to reasons other than chemotherapy,
Patients who do not consent to participate in the study will be excluded.
Exclusion Criteria During the Study
Patients whose taxane treatment protocol is changed,
Patients who have less than four applications per week will be excluded from the study.
Study Design
Study Description
Connect with a study center
Gulhane Education and Research Hospital
Ankara, 06010
TurkeyActive - Recruiting
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