About this trial
This randomized controlled clinical trial aims to evaluate the effect of electroacupuncture combined with self-acupressure on the quality of life of early-stage breast cancer patients receiving chemotherapy.
Eligibility criteria
Qualifiers
Aged 18 years or older and aged 75 years or younger, inclusive. with an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2;
Patients who have not received prior chemotherapy and are scheduled to receive at least 4 cycles of adjuvant or neoadjuvant chemotherapy or combination targeted therapy;
Normal organ function with platelets ≥ 100*10^9/ L, hemoglobin ≥ 90 g/L, serum creatinine ≤ 1.5 mg/dl (133 mmol/L), or creatinine clearance ≥ 60 ml/min, total bilirubin ≤ 1.5 times the upper limit of normal (ULN), alanine aminotransferase ≤ 2.5 times ULN, and aspartate aminotransferase ≤ 2.5 times ULN;
Premenopausal women need appropriate contraception;
Disqualifiers
Patients with needle phobia or allergy to stainless steel needles; and
Current diagnosis of mental illness (e.g., major depression, obsessive-compulsive disorder, or schizophrenia);
History of autoimmune diseases, blood disorders, or organ transplantation, or long-term use of hormones or immunosuppressants;
Comorbid bleeding disorders or thyroid dysfunction;
Trial design
Treatments tested in this trial
- electroacupuncture+ self-acupressure
- sham electroacupuncture + sham self-acupressure
Treatment groups
Sponsors and collaborators
Jiuda Zhao
Lead sponsor
Affiliated Hospital of Qinghai University
Sponsor institution