Foot Bath and Chemotherapy Induced Fatigue
Chemotherapeutic Toxicity, Chemotherapy-induced Fatigue
About this trial
This is an interventional supportive care trial for Chemotherapeutic Toxicity focused on measuring Chemotherapy Induced Fatigue, Warm salt water foot bath
Eligibility Criteria
Inclusion Criteria:
- Receiving adjuvant or neoadjuvant chemotherapy with the diagnosis of early stage cancer
- Having fatigue severity of 3 and >3
- Agreeing to participate in the study.
Exclusion Criteria:
- Having the complaint of peripheral neuropathy.
- Being diagnosed with diabetes
- Having impaired skin integrity.
Sites / Locations
- Outpatient Chemotherapy Unit of the Institute of Oncology in Istanbul University
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Warm Salt Water Foot Bath Group
Control Group
In the first interview Patient Identification Form, Fatigue Severity and Piper Fatigue Scale (PFS) were applied to the patients. A training booklet about chemotherapy-induced fatigue containing the definition, causes, ad development process of chemotherapy-induced fatigue and effective coping approaches were delivered to patients. Each patient received iodine salt and a liquid thermometer to measure the temperature of the water. The patients were asked 1 day after the treatment to apply warm salt water bath of 41-42ºC once a day for 20 minutes for 7 days. Subsequently, the fatigue level of the patients was evaluated 30 minutes after having a warm saltwater foot bath and recorded by questioning via calling them with phone every day and using the Visual Fatigue Scale for 7 days. In the last interview PFS was used to evaluate the effect level of fatigue on the quality of life and the assessment process was completed.
A training booklet about chemotherapy-induced fatigue In the first interview Patient Identification Form, Fatigue Severity and Piper Fatigue Scale were applied to the patients. A training booklet about chemotherapy-induced fatigue containing the definition, causes, ad development process of chemotherapy-induced fatigue and effective coping approaches were delivered to experimental group. Subsequently, the fatigue level of the patients was evaluated and recorded by questioning via calling them with phone every day and using the Visual Fatigue Scale for 7 days. The patients were evaluated in the evening. In the last interview conducted with the patient on the 7th day, Piper's Fatigue Scale was used to evaluate the effect level of fatigue on the quality of life and the assessment process was completed.