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The goal of this clinical trial is to verify the effectiveness and safety of the low load blood flow restriction training program. The intervention effect, tolerance and compliance of low load blood flow restriction training and progressive resistance training on lung cancer patients complicated with sarcopenia during chemotherapy will be compared, in order to provide new ideas for improving or reversing sarcopenia.
The main questions it aims to answer are:
Can low load blood flow restriction training improve sarcopenia in chemotherapy induced lung cancer patients? Which training method is more effective and tolerable between low load blood flow restriction training and progressive resistance training?
Participants will be randomly divided into 3 groups:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Routine care group (Control group, CON) | No Intervention | During hospitalization, patients will be given routine exercise and dietary guidance. | |
| Low load blood flow restriction training group (LL-BFRT) | Experimental | On the basis of routine care, participants who meet the inclusion and exclusion criteria will be guided to undergo low-load blood flow restriction training. Based on the constructed "Low load Blood Flow Restriction Training Program for Chemotherapy Stage Lung Cancer Patients with Sarcopenia", participants will be guided to undergo low-load blood flow restriction training. |
|
| Progressive resistance training group (PRE) | Active Comparator | On the basis of routine care, progressive resistance training will be conducted on subjects who meet the inclusion and exclusion criteria, guided by the progressive resistance training program for malignant tumor patients in the "ACSM Exercise Testing and Exercise Prescription Guidelines: 10th Edition" published by the People's Health Press. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Low load blood flow restriction training | Behavioral | Low load blood flow restriction training will be conducted on the subjects three times a week. Each training session includes upper and lower limb training, with 4 groups trained and repeated 30, 15, 15, and 15 times for each group. Train for a total of 12 weeks.The resistance strength will remain at 30% RM for weeks 1-12. |
| Measure | Description | Time Frame |
|---|---|---|
| Grip strength | The grip strength of the participant's preferred hand | Grip strength will be measured at 3, 6, 9, and 12 weeks after intervention |
| Appendicular Skeletal Muscle Index (ASMI) | Using a human body composition analyzer (ICOMEON-FI2001B) to measure the skeletal muscle mass (ASM) of the limbs, and calculating ASMI using a formula. ASMI=ASM/height^2 | ASMI will be measured at 3, 6, 9, and 12 weeks after intervention |
| Step speed | Measure the walking speed of 6m | Step speed will be measured at 3, 6, 9, and 12 weeks after intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Body mass index (BMI) | Measure height and weight using height measuring instruments and scales | BMI will be measured at 3, 6, 9, and 12 weeks after intervention |
| Quality of life for lung cancer patients |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Xin Wang | graduate student | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The First Affiliated Hospital, Zhejiang University School of Medicine | Hangzhou | Zhejiang | 310020 | China |
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| Progressive resistance training group | Behavioral | The subjects will undergo progressive resistance training three days a week, three groups per day, with each group repeating 10 times. Training includes upper and lower limbs. The resistance load increases over time, with a resistance load of 30% RM for weeks 1-4, 50% RM for weeks 5-8, and 70% RM for weeks 9-12. |
|
Using the QLQ-LC 43 scale to measure the quality of life in lung cancer patients
| Quality of life for lung cancer patients will be measured at 3, 6, 9, and 12 weeks after intervention |
| Exercise compliance | This includes participation rate, interruption rate (number of missed training sessions), termination rate (termination of training before 12 weeks), and dose adjustment rate (adjustment of training load or frequency) | Exercise compliance will be measured at12 weeks after intervention |
| Exercise safety | Record the frequency and time of adverse events caused by exercise, such as muscle pain, joint pain, dizziness, skin bruising, etc., and calculate the incidence rate of adverse events | Exercise safety will be measured at12 weeks after intervention |
| ID | Term |
|---|---|
| D055948 | Sarcopenia |
| D008175 | Lung Neoplasms |
| ID | Term |
|---|---|
| D009133 | Muscular Atrophy |
| D020879 | Neuromuscular Manifestations |
| D009461 | Neurologic Manifestations |
| D009422 | Nervous System Diseases |
| D001284 | Atrophy |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D012816 | Signs and Symptoms |
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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