Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Comprehensive Prehabilitation Program for Locally Advanced Esophagogastric Cancer

Official title: A Comprehensive Preoperative and Postoperative Program Consisting Of Active Physical Therapy, A Comprehensive Nutritional Plan, And Psychological Support For Patients With Locally Advanced, Resectable Cancer Of The Esophagus, Gastroesophageal Junction, and Stomach

Run by Masaryk Memorial Cancer Institute · NCT07671625 · Data updated 2026-11-12

This trial tests if a personalized prehabilitation plan with nutrition, exercise, and psychological support helps patients with locally advanced esophageal, GEJ, or gastric cancer before surgery.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorMasaryk Memorial Cancer Institute
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Brno)
StatusRecruiting
StartedMay 2, 2023
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedJune 26, 2026
Trial IDNCT07671625 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with locally advanced esophageal, GEJ, or gastric cancer planned for comprehensive perioperative therapy and resection, with ECOG 0-2 and ability to participate in a fitness program.

Probably not a fit

Patients with disseminated disease, poor functional status, or inability to engage in exercise or adhere to the nutritional plan may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Patients with locally advanced esophageal, GEJ, or gastric cancer undergoing perioperative therapy and surgery will receive an integrated prehabilitation program including tailored nutrition, an at-home exercise plan, ERAS-inspired perioperative care, and ongoing psychological support. The study aims to see whether these measures improve fitness, recovery, and postoperative outcomes compared with standard care. HRV and aerobic capacity will be monitored to gauge autonomic and cardiorespiratory changes during the preoperative period. The approach targets optimizing physical condition and well-being to reduce perioperative morbidity in a context where treatment can be harsh. The program is designed to be feasible for patients who can participate in exercise and follow a nutritional plan.

Why it matters

Potential benefit: If successful, patients may experience better preoperative fitness, fewer complications after surgery, and faster recovery.

How similar studies have gone: Evidence from prior ERAS and prehabilitation efforts suggests improvements in recovery and perioperative outcomes, though this specific integrated program is novel in this cancer subset.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Consent to participate in the study
* Age ≥ 18 years
* Patients with locally advanced esophageal or gastric cancer indicated for comprehensive perioperative treatment
* Resectable disease
* ECOG performance status 0-2
* Ability to participate in a fitness program
* Willingness to follow a nutritional plan and recommendations

Exclusion Criteria:

* Disseminated disease

Where it's running

  • Masaryk Memorial Cancer Institute
    Brno, Czechia
    Recruiting

Study contacts

  • Principal investigator: Radka Lordick Obermannová, Doc, MD, PhD — Masaryk Memorial Cancer Institute
  • Study coordinator: Martina Lojová, PhD
  • Email: martina.lojova@mou.cz
  • Phone: +420543136232

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.