About this trial
This randomized controlled trial aims to determine the optimal exercise intensity for improving postoperative recovery in patients with upper gastrointestinal cancer. Participants who have undergone curative surgery will be randomly assigned to high-intensity interval training (HIIT), low-intensity continuous training (LICT), or usual care. The exercise interventions will be performed under supervision three times per week for eight weeks. The primary outcome is peak oxygen uptake (VO₂peak), assessed using cardiopulmonary exercise testing. Secondary outcomes include physical function, body composition, patient-reported outcomes, and biological and mechanistic markers such as inflammatory biomarkers, muscle-related factors, and gut microbiota. This study will also explore potential mechanisms underlying exercise-induced adaptations and their association with clinical outcomes.
Eligibility criteria
Qualifiers
Age ≥ 18 years
Diagnosed with esophageal or gastric cancer
Received curative surgery
6 ± 2 weeks after surgery
Disqualifiers
Communication difficulties
Poor general status
Undergone combined laryngopharyngectomy
Unsuitable for evaluation or exercise intervention
Trial design
Treatments tested in this trial
- High-Intensity Interval Training (HIIT)
- Low-Intensity Continuous Training (LICT)