ENERGY: Effect of Exercise and Enteral Nutrition on Survival

Sponsor
The First Hospital of Jilin University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05959226
Collaborator
(none)
960
2
60

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise Intervention
  • Dietary Supplement: Nutrition Intervention
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
960 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of Exercise and Enteral Nutrition Intervention on Survival in Patients With Locally Advanced Gastric Cancer: a Prospective Multicenter Randomized Controlled Study
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2026
Anticipated Study Completion Date :
Aug 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: Exercise and Enteral Nutrition Intervention

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

Behavioral: Exercise Intervention
Nutrition intervention: From discharge (7-14 days after surgery) until 6 months after surgery, patients are required to take 400 kcal/day of oral nutrition supplement (ONS) in addition to their normal diet.. 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;

Dietary Supplement: Nutrition Intervention
(1) Nutrition intervention: From discharge (7-14 days after surgery) until 6 months after surgery, patients are required to take 400 kcal/day of oral nutrition supplement (ONS) in addition to their normal diet..

Active Comparator: Enteral Nutrition Intervention

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

Dietary Supplement: Nutrition Intervention
(1) Nutrition intervention: From discharge (7-14 days after surgery) until 6 months after surgery, patients are required to take 400 kcal/day of oral nutrition supplement (ONS) in addition to their normal diet..

Outcome Measures

Primary Outcome Measures

  1. 3-year overall survival rate [3 years after surgery]

    The 3-year overall survival rate refers to the proportion of gastric cancer patients who have survived for more than 3 years after various comprehensive treatments

Secondary Outcome Measures

  1. 3-year disease-free survival rate [3 years after surgery]

    The proportion of clinically confirmed complete remission to recurrence within 3 years

  2. Scored Patient-Generated Subjective Global Assessment, PG-SGA [6 months after surgery]

    Scored Patient-Generated Subjective Global Assessment is the preferred method recommended by the American Dietitian Association for nutritional screening of tumor patients. It can conduct qualitative and quantitative comprehensive evaluation of patients' nutritional status from four aspects: weight loss, disease and age, metabolic stress status, and physical examination. It is a sensitive evaluation scale for patients to malnutrition changes

  3. QLQ-C30 assessment [6 months after surgery]

    The quality of life of patients 6 months after surgery was evaluated using the European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire (QLQ-C30), which can evaluate the quality of life from a multidimensional perspective and better reflect the connotation of quality of life. It is widely used in clinical practice to measure the quality of life of cancer patients.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • The First Hospital of Jilin University

Investigators

  • Principal Investigator: Quan Wang, Dr, The First Hospital of Jilin University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Quan Wang, Professor, The First Hospital of Jilin University
ClinicalTrials.gov Identifier:
NCT05959226
Other Study ID Numbers:
  • STARS-GC07
First Posted:
Jul 25, 2023
Last Update Posted:
Jul 25, 2023
Last Verified:
Jul 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 25, 2023