Breast Cancer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Medical staff: 1. Legal practitioners in the medical industry who meet the regulations of the National Health Commission in 2023 and have a professional qualification certificate; 2. Have experience in breast surgery, and have a certain understanding of postoperative rehabilitation of breast cancer; 3. Able to proficiently fill out online questionnaires and voluntarily participate in this study; 4. Willing to participate in research and accept ethical committee review. Patient data: 1. Postoperative patients with breast malignant tumors; 2. The patient has received upper limb functional exercise training after surgery; 3. Clear thinking, proficient in filling out online questionnaires, and willing to participate in this study; 4. Patients have complete rehabilitation data records during the study period, which can be used for subsequent analysis; 5. Willing to participate in research and accept ethical committee review.
Exclusion criteria
Exclusion criteria: Medical staff: 1. Medical staff who do not have experience in breast surgery or do not involve in rehabilitation guidance after breast cancer surgery; 2. Medical staff who have resigned for more than 2 years or no longer engaged in related work during the research period; 3. Training or education personnel: medical staff who are dedicated to non clinical work such as training and education; 4. Medical staff who did not obtain informed consent or did not agree to participate in the study. Patient data: 1. Merge other serious systemic diseases (such as severe heart disease, renal failure, severe liver disease, etc.); 2. There is already obvious upper limb dysfunction before surgery (such as upper limb function impairment caused by restricted limb movement or other serious diseases); 3. Patients who experience serious complications after surgery, such as severe infection, non healing wounds, postoperative bleeding, etc., which may affect the recovery process; 4. Patients who are unable to understand or implement rehabilitation guidance due to cognitive impairments (such as Alzheimer's disease, mental illness, etc.); 5. Pregnant or lactating patients may have an impact on their recovery process due to hormonal changes; 6. Patients who explicitly refuse to participate in the study; 7. Patients who lack necessary rehabilitation data records or have their rehabilitation process stopped midway.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cognition of medical staff on time point of upper limb rehabilitation guidance after breast cancer surgery;Frequency of upper limb rehabilitation guidance after breast cancer surgery Cognition of medical staff;Awareness of medical staff on guidance intensity of upper limb rehabilitation after breast cancer surgery;Patients' cognition on time point of upper limb rehabilitation guidance after breast cancer surgery;Cognition of patients with upper limb rehabilitation guidance frequency after breast cancer surgery;Cognition of patients with upper limb rehabilitation guidance intensity after breast cancer surgery; | — |
Secondary
| Measure | Time frame |
|---|---|
| General information of medical staff participating in this study;General information of patients participating in this study; | — |
Countries
China
Contacts
Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine