- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04439734
Effects of Whole-body Electromyostimulation on Golf Performance in Amateur Golfers
Effects of Whole-body Electromyostimulation on Clubhead Speed and Stability in Ambitious Amateur Golfers - a Randomized Controlled Trial.
Golf is becoming increasingly popular in Germany. However, the biomechanical and motor challenge of golf should not be underestimated. Nevertheless, only very few amateur golfers carry out serious preparation and conditioning as part of a strength/stabilization program. The main argument for this limitation is the aspect of "limited time resources". A solution to this problem could therefore be the time-effective and highly individualizable whole-body electromyostimulation (WB-EMS) technology.
The aim of the present study is to evaluate the effectiveness of 16 weeks of WB-EMS application on trunk stability and clubhead speed in male amateur golfers in a (randomized) controlled setting.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Erlangen, Germany, 91052
- Institute of Medical Physics, Friedrich-Alexanden University Erlangen-Nürnberg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Golfhandicap ≤20,
- members of the Golfclub München-Eichenried
Exclusion Criteria:
- diseases and medication that did not allow WB-EMS training (see contraindications WB-EMS) or enable proper assessment of clubhead speed (in cases of doubt, individual medical decision),
- resistance and/or WB-EMS Training during the last 6 months,
- more than two expected missed WB-EMS sessions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Whole-Body Electromyostimulation
WB-EMS once per week for for 16 week (85 Hz, 350 µs, bipolar, duty cycle 4s-4s)
|
WB-EMS once per week 20 min for 16 weeks
|
|
No Intervention: Non WB-EMS control
No WB intervention, but maintained physical activity and habitual exercise habits
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Clubhead speed
Time Frame: At baseline and after16 weeks (i.e. over 16 weeks)
|
Changes of clubhead speed as determined by a radar-based system ("TrackMan", Scottsdale, USA)
|
At baseline and after16 weeks (i.e. over 16 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trunk stability as determined by
Time Frame: At baseline and after16 weeks (i.e. over 16 weeks)
|
Changes of maximum isometric trunk strength (index of trunk extension/-flexion; lateral flexion and trunk rotation) as determined by an isometric testing device
|
At baseline and after16 weeks (i.e. over 16 weeks)
|
|
Clubhead speed
Time Frame: At baseline and after 8 weeks (i.e. over 8 weeks)
|
Changes of clubhead speed as determined by a radar-based system ("TrackMan", Scottsdale, USA)
|
At baseline and after 8 weeks (i.e. over 8 weeks)
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Zink C, Rückel F, von Stengel S, Kemmler W. The Use of Whole Body Electromyostimulation (WB-EMS) as a Golf Warm-Up - A Randomized Controlled Cross-Over Study. Archives of Physical Health and Sports Medicine 2019; 2(1)1: 04-12
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- GOLFEMS III
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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