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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03417323
Other study ID # Compression_DOMS_EMS
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 10, 2017
Est. completion date May 31, 2018

Study information

Verified date July 2018
Source University of Erlangen-Nürnberg Medical School
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study address two main topics:

1. The effect of compression garment on whole-body electromyostimulation (WB-EMS) induced muscle soreness in young adults

2. The repeated bout effect of one intense session of WB-EMS as determined by various regeneration parameters


Description:

Using a cross-over design we applied 2 intense WB-EMS training sessions either with or without subsequent wearing of compression garments (long tights) for 5 days at baseline and after a washout period of 4 weeks. Healthy young to middle aged athletes used compression garments immediately postexercise for 24 hours and further 12 h during the day. Blood samples, questionnaires, resting metabolic rate and performance test were applied prior and 24, 48,72 and 96 h post-exercise consistently without wearing compression garments.


Recruitment information / eligibility

Status Completed
Enrollment 23
Est. completion date May 31, 2018
Est. primary completion date February 22, 2018
Accepts healthy volunteers No
Gender Male
Age group 25 Years to 50 Years
Eligibility Inclusion Criteria:

- healthy athletes with >5 years of experience in competition balls sports and corresponding discipline specific resistance exercise

Exclusion Criteria:

- diseases and medication affecting muscle metabolism

- contraindication for WB-EMS

Study Design


Intervention

Other:
Compression
Participants in the treatment group wear compression garment after intense WB-EMS application for 24 h, and 12 h for day 2, 3, 4 post WB-EMS.

Locations

Country Name City State
Germany Institute of Medical Physics University of Erlangen-Nurnberg Erlangen
Germany Institute of Medical Physics, University of Erlangen-Nurnberg Erlangen

Sponsors (2)

Lead Sponsor Collaborator
University of Erlangen-Nürnberg Medical School German Sport University, Cologne

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Kemmler W, Teschler M, Bebenek M, von Stengel S. [(Very) high Creatinkinase concentration after exertional whole-body electromyostimulation application: health risks and longitudinal adaptations]. Wien Med Wochenschr. 2015 Nov;165(21-22):427-35. doi: 10.1007/s10354-015-0394-1. Epub 2015 Oct 26. German. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Maximum isokinetic leg extensor strength Changes of isokinetic leg extensor strength during the intervention period 5 days
Secondary Perceived physical state Changes of perceived physical state as determined by the WKV-scale (Kleinert, 2001) during the intervention period 5 days
Secondary Resting metabolic rate Changes of resting metabolic rate during the intervention period 5 days
Secondary Myoglobin Changes of myoglobin-levels during the intervention period 5 days
Secondary Heart rate variability Changes of Heart rate variability during the intervention period 5 days
Secondary creatine-kinase (CK) concentration Changes of CK-levels during the intervention period 5 days

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