Clinical Trial Matcher

NCT06414122

Modulated Mid-frequency Whole-body Electromyostimulation and Nutritional Therapy in Gastrointestinal Cancer Patients

Not Yet Recruiting · Not Applicable · University of Cologne · registry updated 2026-07-27

Inclusion and exclusion lines below are quoted from ClinicalTrials.gov. No match score is shown, because a score needs a person's age, biomarkers, and treatment dates. Confirm the record with the study team.

The purpose of this study is to assess the efficacy of modulated mid-frequency whole-body electromyostimulation (WB-EMS) combined with nutritional therapy in patients with gastrointestinal cancer.

Inclusion

  • Patients with oesophageal, gastric, duodenal, colon or rectal cancer following surgery without further therapy and with neoadjuvant and adjuvant therapy
  • medical clearance for exercise training
  • written declaration of consent from the study participant

Exclusion

  • Participation in another study on the topic of exercise or nutrition
  • Electronic implants such as pacemakers, pumps, and coronary stents
  • Cardiac arrhythmia
  • Implants in the area of application (e.g. breast implants)
  • Wounds and open skin diseases in the area of application of the electrodes
  • Unhealed operations or bone fractures

Open NCT06414122 on ClinicalTrials.govAll conditions

Modulated Mid-frequency Whole-body Electromyostimulation and Nutritional Therapy in Gastrointestinal Cancer Patients | Clinical Trial Matcher