Actively Recruiting
Exercise and Cardiorespiratory Fitness Improvement Through Supervised Training in Upper Gastrointestinal Cancer Surgery Patients (EXCITING-UGI)
Led by Kansai Medical University · Updated on 2026-05-19
171
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how different exercise intensities affect recovery after surgery in patients with upper gastrointestinal cancer, including esophageal and gastric cancer. This randomized controlled trial compares high-intensity interval training (HIIT), low-intensity continuous training (LICT), and usual care to understand which approach best improves physical fitness and other health outcomes. The study also investigates biological markers to explore how exercise influences recovery at a physiological level. Participants begin the study about 6 weeks after surgery and are randomly assigned to one of three groups. The HIIT group performs supervised aerobic interval training combined with resistance exercises three times a week for eight weeks, while the LICT group completes continuous low-intensity aerobic and resistance training on the same schedule. Both exercise groups receive nutritional counseling every four weeks. The usual care group receives standard postoperative care with nutritional counseling but no structured exercise. During the study, participants undergo assessments of peak oxygen uptake using cardiopulmonary exercise testing at the start and after eight weeks. Researchers also measure physical function, muscle mass, physical activity levels, quality of life, and collect blood and gut microbiome samples. Exercise adherence and safety are monitored throughout. The total participation includes the eight-week intervention period with follow-up evaluations to understand recovery progress.
CONDITIONS
Brief Title
Exercise Training After Upper Gastrointestinal Cancer Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosed with esophageal or gastric cancer
- Received curative surgery for cancer
- 6 ± 2 weeks after surgery
- Able to provide written informed consent
You will not qualify if you...
- Difficulty communicating
- Poor overall health status
- Underwent combined laryngopharyngectomy
- Unsuitable for evaluation or exercise intervention
- Considered unsuitable for the study by the primary physician
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 weeks
Participants perform supervised exercise training three times per week for eight weeks, which includes aerobic and resistance training. Nutritional counseling is provided once every four weeks for a total of two sessions. Participants are randomly assigned to high-intensity interval training, low-intensity continuous training, or usual care.
Three exercise sessions per week and 2 nutritional counseling visits
Trial Site Locations
Total: 2 locations
1
Kansai Medical University
Hirakata, Osaka, Japan, 573-1136
Not Yet Recruiting
2
Kansai Medical University
Hirakata, Osaka, Japan, 573-1136
Actively Recruiting
Research Team
T
Takuya Fukushima
J
Jiro Nakano
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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