Exercise Training After Upper Gastrointestinal Cancer Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKansai Medical University

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)

Treatment groups

171 Participants
are divided into 3 treatment groups

Sponsors and collaborators