None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults aged 19 years or older diagnosed with cancer who have undergone chemotherapy at least once. 2. Patients currently experiencing sensory symptoms (pain, numbness, etc.) related to chemotherapy-induced peripheral neuropathy (CIPN) and reporting symptoms in the sensory domain of the EORTC QLQ-CIPN20. 3. Inpatients at the study site or those scheduled for continuous hospitalization during the study period. 4. Patients capable of communication who have voluntarily provided written informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients with central or peripheral nervous system diseases unrelated to chemotherapy (e.g., stroke, Parkinson's disease, spinal cord injury). 2. Patients with unstable systemic conditions (e.g., acute infection, fever) for whom the intervention is deemed unsafe. 3. Patients with moderate to severe cognitive impairment or difficulty in communication/consent. 4. Patients on complete bed rest or with limited voluntary movement preventing exercise participation. 5. Patients with open wounds, skin lesions, or diabetic foot issues on lower extremities preventing footbath. 6. Patients receiving other intensive non-pharmacological interventions for CIPN concurrently during the study period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Chemotherapy-Induced Peripheral Neuropathy Symptom Score (Assessed by EORTC QLQ-CIPN20) | — |
Secondary
| Measure | Time frame |
|---|---|
| Fatigue Level Score (Assessed by EORTC QLQ-FA12) | — |
Countries
Korea, Republic of
Contacts
Jeonbuk National University