Effect of Exercise and Enteral Nutrition on Survival (ENERGY)

Jilin University

Status: Not yet enrolling

Conditions: Gastric Cancer; Sarcopenia; Nutrition Related Cancer

Treatments: Behavioral: Exercise Intervention; Dietary Supplement: Nutrition Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT05959226

STARS-GC07

Details and patient eligibility

About

The present clinical trial was designed to explore the effect of postoperative physical exercise combined with enteral nutritional supplement on 3-year disease-free survival in patients with advanced gastric cancer.

Full description

The present clinical trial was designed to explore the effect of physical exercise combined with enteral nutritional supplement on 3-year disease-free survival in patients with advanced gastric cancer. In the trial group, comprehensive postoperative management model with targeted exercise intervention and nutritional support. The details are as follows:

1. Nutrition intervention: From discharge (7-14 days after surgery) until 6 months after surgery, patients are required to take 400 kcal/day of enteral nutrition supplement (ONS) in addition to their normal diet. Once the patient's oral diet decreases, ONS will be added several times a day to ensure that the total energy reaches the ESPEN recommended daily 30 kcal/kg. The daily protein requirement is set at 1.2-1.5 g/kg of actual body weight. The Dietitian will keep records and help patients adjust their energy intake weekly.
2. Exercise: under the guidance of the rehabilitation therapist, the patient gradually recovers Exercise from discharge (7-14 days after the operation) to 6 months after the operation, and should ensure at least 150 minutes of moderate intensity exercise or a combination of equivalent activities per week; The control group patients received the same baseline evaluation as the experimental group patients. The control group will not receive phisical exercise intervention, but will receive postoperative nutritional treatment with the same standards as the experimental group.

Enrollment: 960 estimated patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:（1) 18 years ≤ age ≤ 70 years (2) Preoperative Karnofsky physical condition score: 0 or 1 or 2 (3) Preoperative pathological biopsy by gastroscope, histologically confirmed as adenocarcinoma (papillary adenocarcinoma, tubular adenocarcinoma, mucinous adenocarcinoma, Signet ring cell carcinoma, poorly differentiated adenocarcinoma, mixed adenocarcinoma) (4) Gastric cancer patients diagnosed with clinical stage Ib IIIc through CT, MRI, gastroscopy, and pathology (based on the 8th edition of UICC/AJCC staging) (5) Abdominal enhanced CT/MRI examination showed a clinical staging of cT2-4aN0-3M0 (based on AJCC-8thTNM tumor staging), and standard D2 radical surgery for gastric cancer was performed; (6) Have not received any radiotherapy, chemotherapy or immunotherapy; (7) Hemoglobin ≥ 80g/L; (8) Absolute neutrophil count (ANC) ≥ 1.5 × 109/L; (9) Platelets ≥ 75 × 109/L; (10) ALT ≤ 2.5 times the normal upper limit value; (11) AST ≤ 2.5 times the normal upper limit value; (12) ALP ≤ 2.5 times the normal upper limit value; (13) Serum total bilirubin<1.5 times the upper normal limit value; (14) Serum creatinine<1 times the upper normal limit value; (15) Sign written informed consent;

Exclusion Criteria:

1. Patients diagnosed with distant metastasis through abdominal lung CT/MRI or PET-CT
2. Pregnant or lactating women
3. People with uncontrolled epilepsy, Central nervous system disease or mental disorders
4. Patients with combined limb disabilities or motor dysfunction;
5. Patients with other malignant diseases in the past five years, excluding cured skin cancer and cervical Carcinoma in situ
6. Clinically severe (i.e. active) heart disease, such as symptomatic coronary heart disease, New York Heart Association (NYHA) grade II or more severe congestive heart failure, or severe arrhythmia requiring medication intervention, or a history of myocardial infarction within the past 6 months
7. Have a history of cerebral infarction or cerebral hemorrhage in the past 6 months
8. Organ transplantation requires immunosuppressive therapy
9. Serious uncontrolled recurrent infections or other serious uncontrolled concomitant diseases
10. The patient has complications of Grade III or above in Clavien Dindo classification or has been hospitalized for more than 14 days after surgery due to various reasons;
11. Urgent surgery required due to tumor emergencies (bleeding, perforation, obstruction)
12. Pulmonary function test FEV1<expected value 50%
13. Received radiotherapy, chemotherapy, or other neoadjuvant treatment before surgery

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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960 participants in 2 patient groups

Exercise and Enteral Nutrition Intervention

Experimental group

Description:

A comprehensive postoperative management combined physical exercise intervention with oral nutritional support

Treatment:

Dietary Supplement: Nutrition Intervention

Behavioral: Exercise Intervention

Enteral Nutrition Intervention

Active Comparator group

Description:

The control group will not receive exercise intervention, but will receive postoperative nutritional support treatment with the same standards as the experimental group.

Treatment:

Dietary Supplement: Nutrition Intervention