None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients diagnosed with cancer and who receive chemoport with chemotherapy 2) Patients who were diagnosed with cancer and had wounds healed more than 2 months after chemoport procedure for chemotherapy 3) Patients with no dermatological lesions at the chemoport puncture site and without inflammatory reactions or circulatory disorders 4) Adult patients over 19 years of age who have no mental deficits, who can understand and answer the experiments and are able to communicate. 5) Patients who have not received other pain relievers when inserting chemoport needles 6) Patients who understand the purpose of this study and allow participation
Exclusion criteria
Exclusion criteria: 1) Hospice patients with terminal cancer who have a life expectancy of less than 6 months 2) Patients deemed difficult to self-determining participation and rejection due to unclear consciousness or difficulty in communication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety | — |
Countries
Korea, Republic of
Contacts
Yonsei University