Transcutaneous Electrical Acupoint Stimulation for Non-small Cell Lung Cancer Patients
Non-Small Cell Lung Cancer, Lung Cancer
About this trial
This is an interventional treatment trial for Non-Small Cell Lung Cancer focused on measuring Acupuncture, electrical stimulation of acupoints, chemotherapy, Diyu Shengbai Pian, nursing care
Eligibility Criteria
Inclusion Criteria:
- diagnosis of Non-small cell lung cancer(NSCLC)
- age between 20 and 75 years
- chemotherapy naive after diagnosis
- GP regimen as treatment
- an expected survival of more than 12 weeks based on a score equal to or greater than 60 points on Karnofsky performance status (KPS) scale
- the ability to understand and speak Mandarin
Exclusion Criteria:
- diagnosis of a hematological system tumor
- mental illness
- bone marrow suppression prior to chemotherapy
- pregnancy
Sites / Locations
- Shanghai Pulmonary Hospital Medical Oncology DepartmentRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
No Intervention
TEAS group
Medication group
Control group
Patients with transcutaneous electrical acupoint stimulation (TEAS) group receive electrical stimulation of acupoints including Dazhui (DU14), Geshu (BL17), Zusanli (ST36), Sanyinjiao (SP6), and Hegu (LI4).
On the basis of routine nursing care, patients need to take Sanguisorba officinalis L., named Diyu Shengbai Pian (a Traditional Chinese Medicine) 3 times per day.
The patients of control group receive routine nursing care, including (1) to be observed the changes in patient condition, (2) to eat high-calories, high-protein, high-vitamin, easy-to-digest foods during chemotherapy, (3) to be treated by psychological care, (4) to be prevented against the occurrence of phlebiti, and (5) to use Ondansetron and Omeprazole as direction.