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Not yet recruiting NCT07201857

Peri-habilitation for Patients With Gastric Cancer

No phase Interventional Gastric Cancer (Diagnosis) Gastric Cancer Patient Gastric Cancer Patients Undergoing Gastrectomy Gastric Cancer Patients Undergoing Minimally Invasive Gastrectomy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: nutrition education plus active supplement, Exercise.
Who it may be relevant to
Registry conditions: Gastric Cancer (Diagnosis), Gastric Cancer Patient, Gastric Cancer Patients Undergoing Gastrectomy, Gastric Cancer Patients Undergoing Minimally Invasive Gastrectomy. Basic parameters: 65 years — 90 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Peri-habilitation to Enhance Treatment Outcomes and Postoperative Recovery in Patients With Gastric Cancer

Overview

This study aims to evaluate the clinical applicability of a peri-habilitation program in patients with gastric cancer by applying nutritional intervention for approximately two weeks before surgery and a combined exercise and nutrition intervention for about three weeks after hospital discharge, and by analyzing its effects on the prevention of postoperative complications and recovery.

Interventions

  • Dietary supplement nutrition education plus active supplement
    Nutrition Group (NUT) Participants will receive standard clinical care combined with nutrition education and protein-enriched soy milk supplementation for approximately 2 weeks before surgery and about 3 weeks after hospital discharge.
  • Behavioral Exercise
    Exercise and Nutrition Participants will receive peri-habilitation exercise training together with nutritional intervention, including carbohydrate plus protein-enriched soy milk supplementation twice daily (before and after exercise), for approximately 2 weeks before surgery and about 3 weeks after hospital discharge.

Primary outcome measures

  • Gait speed test [Time frame: Baseline (2 weeks before surgery) Preoperative hospitalization (1-4 days before surgery) Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]
  • Chair stand test [Time frame: Baseline (2 weeks before surgery) Preoperative hospitalization (1-4 days before surgery) Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]
  • Balance test [Time frame: Baseline (2 weeks before surgery) Preoperative hospitalization (1-4 days before surgery) Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]
  • Timed up and go test [Time frame: Baseline (2 weeks before surgery) Preoperative hospitalization (1-4 days before surgery) Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]
Secondary outcome measures (5)
  • Electrocardiogram(ECG) [Time frame: Baseline (2 weeks before surgery) Preoperative hospitalization (1-4 days before surgery) Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]
  • Inflammation and Oxidative Stress Markers (Blood Analysis) [Time frame: Baseline (2 weeks before surgery) Preoperative hospitalization (1-4 days before surgery) Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]
  • Hospital Anxiety and Depression Scale (HADS) [Time frame: Baseline (2 weeks before surgery) Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]
  • Quality of life(KOQUSS-32, KOQUSS-40) [Time frame: Baseline (2 weeks before surgery) 3 weeks after discharge 6 months after surgery]
  • Clavien-dindo classification [Time frame: Postoperative discharge (at hospital discharge) 3 weeks after discharge 6 months after surgery]

Eligibility criteria

Inclusion criteria

  • Patients aged 65 years or older who have been diagnosed with gastric cancer and are scheduled to undergo surgical treatment or chemotherapy.

Exclusion criteria

  • Patients with severe conditions who are unable to undergo the intervention prior to surgical treatment or chemotherapy.
  • Patients with physical (e.g., musculoskeletal) or mental disorders that make participation in or continuation of the program impossible.
  • Patients judged to be at risk of additional physical burden from the intervention.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

South Korea · 1 center
  • Anam Hospital — Seoul

Identifiers

NCT: NCT07201857 · KUMCANAM2025GES1

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗