Fact CheckerSign in

NCT06414122Not yet recruiting

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

The Efficacy of Modulated Mid-frequency (Whole-body Electromyostimulation) and Nutritional Therapy in Patients With Solid Tumors of the Gastrointestinal Tract (Excluding Liver and Pancreatic Carcinomas)

Source: ClinicalTrials.gov · Last updated 27 Jul 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
88 (estimated)
First submitted
10 May 2024
Start date
1 Aug 2026
Primary completion date
Aug 2028
Lead sponsor
University of Cologne
NCT number
NCT06414122

What you commit to

  • Study type: Interventional
  • Planned participants: 88
  • From 1 Aug 2026 to the primary completion date, Aug 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Electronic implants such as pacemakers, pumps, and coronary stents
  • Implants in the area of application (e.g. breast implants)
  • Metal and electronic parts in the body (e.g. prostheses, metal vascular clips, hearing aids/inner ear/cochlear implants, magnetic dental prostheses, pacemakers, contraceptives)

Other illness

  • Cardiac arrhythmia
  • Epilepsy
  • Wounds and open skin diseases in the area of application of the electrodes
  • Acute inflammatory diseases (e.g. inflammation of the intervertebral discs, bones, vessels, or soft tissue)
  • Bone diseases with high-grade osteoporosis
  • Increased risk of haemorrhage
  • Fever and illnesses that can be aggravated by physical exertion

Other

  • Participation in another study on the topic of exercise or nutrition
  • Pregnancy
  • Unhealed operations or bone fractures
  • Directly after herniated discs or other instabilities such as large abdominal wall hernias
  • Blood clots (thromboses)
  • Untreated high blood pressure
  • Blindness
  • Continuous parenteral nutrition

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitätsklinikum Köln, Centrum für Integrierte Onkologie (CIO)
Coordinator of this site? Confirm its status
CologneGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.