Effects of Whole-Body Electromyostimulation on Golf Performance

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:
  • Whole Body Electromyostimulation
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.

Clinical Trials on Muscle Strength

Clinical Trials on WB-EMS

3
Subscribe