- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04264416
Effects of Whole-Body Electromyostimulation on Golf Performance
January 7, 2021 updated by: University of Erlangen-Nürnberg Medical School
Effects of 16 Weeks of Whole-Body Electromyostimulation on Stability, Strength and Golf Performance in Amateur Golfers - A Randomized Controlled Study
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-EMSapplication on maximum strength of the lower extremities, trunk stability and (golf) handicap in male amateur golfers in a (randomized) controlled setting.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Bavaria
-
Erlangen, Bavaria, Germany, 91052
- Institute of Medical Physics, Friedrich Alexander University Erlangen-Nürnberg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- golf amateurs with a history if golf > 2 years
- no WB-EMS application during the last 12 months
Exclusion Criteria:
- contraindications for WB-EMS (in doubt assessment by study physician)
- contraindications for MRI (in doubt assessment by study physician)
- resistance exercise training for more one 60 min/week during the last 12 months
- expected absence of more than one week during the intervention period (WB-EMS)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Whole-Body Electromyostimulation
16 weeks of dynamic WB-EMS: one supervised session per week, 20 min session; impulse-frequency: 85 Hz; impulse breadth 350 µs; intermittent 4-6 s; of impulse - 4 s of impulse break; impulse intensity RPE 7 (hard+ to very hard) on Borg CR 10 Scale.
|
16 weeks of WB-EMS
Other Names:
|
No Intervention: Non exercising control
...maintained physical activity and exercise habits during the study period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
18 hole golf score
Time Frame: through study completion, on average 4 months
|
Average golf score of 5 rounds on a 18 hole course (supervised)
|
through study completion, on average 4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hip-/leg extensor strength
Time Frame: At baseline and after 16 weeks
|
Changes of maximum dynamic hip-/leg extensor strength as determine by an isokinetic leg press
|
At baseline and after 16 weeks
|
Trunk strength
Time Frame: At baseline and after 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 after 16 weeks
|
Muscle density at the mid-thigh
Time Frame: At baseline and after 16 weeks
|
Muscle density at the mid-thigh as determined by MRI
|
At baseline and after 16 weeks
|
Muscle density at lumbar spine
Time Frame: At baseline and after 16 weeks
|
Muscle density at the para-vertebral site as determined by MRI
|
At baseline and after 16 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Carina Zink-Rückel, MSc, Institute of Medical Physics, FAU, Germany
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Carina Zink-Rückel, Florian Rückel, Simon von Stengel, Wolfgang Kemmler. 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 Volume 2 (2019)1: 04-12
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 20, 2020
Primary Completion (Actual)
December 30, 2020
Study Completion (Actual)
December 31, 2020
Study Registration Dates
First Submitted
February 6, 2020
First Submitted That Met QC Criteria
February 8, 2020
First Posted (Actual)
February 11, 2020
Study Record Updates
Last Update Posted (Actual)
January 11, 2021
Last Update Submitted That Met QC Criteria
January 7, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- EMSGOLF
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The data that support the findings of this study are available from the responsible researcher [W.
Kemmler], upon reasonable request.
IPD Sharing Time Frame
Immediately after publication and ending 3 years following article publication
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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