Breast cancer
Conditions
Interventions
Trial Group:Personalized exercise prescription based on TCM constitution identification
Control Group:Routine postoperative exercise regimen for breast cancer patients
Trial Group (Pilot Study):Provide patients with exercise prescriptions tailored to their physical conditions
Control Group (Pilot Study):Provide patients with conventional exercise methods
Sponsors
Tianjin Medical University Cancer Institute & Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Pilot Study 1. Patients diagnosed with breast cancer by pathology who have undergone breast cancer surgery; 2. Age >= 18 years; 3. Complete baseline data available for follow-up; 4. Able to cooperate with completing the exercise prescription and survey; 5. Informed consent obtained from the patient and family. Formal Study 1. Patients diagnosed with breast cancer by pathology who have undergone breast cancer surgery; 2. Age >= 18 years; 3. Complete baseline data available for follow-up; 4. Able to cooperate with completing the exercise prescription and survey; 5. Informed consent obtained from the patient and family.
Exclusion criteria
Exclusion criteria: Pilot Study 1. Individuals unable to cooperate with this study due to personal reasons or other objective factors, such as those unable to perform prescribed exercise training at the Rehabilitation Medicine outpatient clinic; 2. Patients with severe chronic diseases such as heart failure or renal failure, or other tumors, whose condition is too severe to participate or cooperate; 3. Individuals concurrently participating in other clinical trials. Formal Study 1. Individuals unable to cooperate with this study due to personal reasons or other objective factors, such as those unable to perform prescribed exercise training at the Rehabilitation Medicine outpatient clinic; 2. Patients with severe chronic diseases such as heart failure or renal failure, or other tumors, whose condition is too severe to participate or cooperate; 3. Individuals concurrently participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Traditional Chinese Medicine Body Type Identification;Far-infrared imaging image analysis;Degree of motor function; | — |
Secondary
| Measure | Time frame |
|---|---|
| Fatigue Severity Scale; | — |
Countries
China
Contacts
Public ContactWu Peipei
Tianjin Medical University Cancer Institute & Hospital
Outcome results
None listed