Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07561840

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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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