Completed

Effects of Whole-Body Electromyostimulation (WB-EMS) Combined With Individualized Nutritional Support on Patients With Malignant Disease Undergoing Curative or Palliative Anti-cancer Treatment

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What is being tested

Whole-Body Electromyostimulation (WB-EMS)

Other
Who is being recruted

Atrophy+15

+ Body Weight

+ Body Weight Changes

Over 18 Years
+11 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: August 2013
See protocol details

Summary

Principal SponsorUniversity of Erlangen-Nürnberg Medical School
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 2013

Actual date on which the first participant was enrolled.

This study evaluates the effects of a 12-week whole-body electromyostimulation (WB-EMS) training combined with individualized nutritional support on body composition, muscle strength and function and quality of life of patients with malignant disease undergoing curative or palliative anti-cancer treatment

Official TitleEffects of Whole-Body Electromyostimulation (WB-EMS) Combined With Individualized Nutritional Support on Patients With Malignant Disease Undergoing Curative or Palliative Anti-cancer Treatment
NCT02293239
Principal SponsorUniversity of Erlangen-Nürnberg Medical School
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

278 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

AtrophyBody WeightBody Weight ChangesCachexiaMuscular AtrophyMuscular DiseasesMusculoskeletal DiseasesNeoplasmsNervous System DiseasesNeurologic ManifestationsPathologic ProcessesSigns and SymptomsPathological Conditions, Signs and SymptomsThinnessWeight LossMuscle WeaknessPathological Conditions, AnatomicalNeuromuscular Manifestations

Criteria

2 inclusion criteria required to participate
malignant disease (solid or hematological cancer): head and neck cancer, colorectal carcinoma, small intestinal cancer, gastric cancer, oesophageal cancer, pancreas carcinoma, liver cell carcinoma, cholangiocarcinoma,lung cancer, breast cancer, cervix cancer, ovarian cancer, prostate cancer, renal cell carcinoma, malignant melanoma, patients with leukaemia and malignant lymphomas or Graft-versus-Host-Disease after bone marrow transplantation

ongoing or planned curative or palliative anti-cancer therapy

9 exclusion criteria prevent from participating
simultaneous participation in other nutritional or exercise intervention trials

acute cardiovascular events

use of anabolic medications

epilepsy

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
physical exercise group regular WB-EMS training (2 EMS trainings per week; each session for 20 min) \+ individualized nutritional support (dietary advices: daily protein intake \> 1.0 g/kg bodyweight)

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Medizinische Klinik 1, University of Erlangen-Nürnberg

Erlangen, GermanyOpen Medizinische Klinik 1, University of Erlangen-Nürnberg in Google Maps
CompletedOne Study Center