breast cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Female, aged > 18 years, hospitalized for breast cancer surgery; 2. Preoperative assessment of PSQI < 7, HAMA < 7, HAMD < 7; 3. Anesthesia for general anesthesia, ASA class I, II; 4. Good mental state, communication barrierless and can complete PSQI, sleep diary, anxiety self-rating scale (FSAS) and other tests; 5. The patient is voluntary and his/her family agrees to participate in this trial, and signs the informed consent.
Exclusion criteria
Exclusion criteria: 1. Allergic constitution, previous allergic to adhesive tape; 2. The external ear skin should not be applied to the stun needle, such as the external ear has damaged, eczema, ulcers, chilblains; 3. Patients with a history of mental illness before surgery; 4. Those with communication disorder, cognitive disorder or previous impaired brain function; 5. Long-term use of sedatives, tricyclic antidepressants (promethazine, clomipraline, amitriptyl, doxet) or long-term drug use; 6. Participating in other clinical investigators.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PSQI;; | — |
Secondary
| Measure | Time frame |
|---|---|
| 15 items of postoperative recovery quality;Hamilton Anxiety Scale;Hamilton Depression Scale;Self-rating fatigue scale;nausea;vomiting;pain;First postoperative exhaust time;Time of first postoperative defecation;Duration of postoperative hospital stay; | — |
Countries
China
Contacts
Jiangsu Provincial Hospital of Traditional Chinese Medicine