Impact of Strength and Power Training on Golf Performance and Swing Biomechanics

August 16, 2019 updated by: Blake Justice, Methodist University, North Carolina
Assess the impact of 10 weeks of strength and power training on Golf performance and swing biomechanics as measured by Trackman radar device and 16-camera monitoring system.

Study Overview

Detailed Description

Golf-specific exercise programs have been shown to improve strength, flexibility, and balance in golfers (1) and golf-specific plyometric training programs have been shown to significantly improve club head speed and ball carry distance in skilled adolescent golfers (2). Further, leg power, upper body strength, and arm strength have positively correlated with golf performance measures; most notably measures of distance and total score (3). The purpose of this study is to assess the effect of a 10-week strength and power training program on the biomechanics of the golf swing and golf performance.

Participants will have anthropometric data taken, including height, weight, and body composition.

Golf swing biomechanics will be assessed utilizing high-speed motion analysis cameras and software available in the Motion Analysis Laboratory in the McLean Health Sciences Building. The participant will don garments that fit snug to the skin and light-sensitive reflective markers will be placed on the subject. The motion of the swing will be captured utilizing the 14 camera Vicon Bonita 10 system with the Motion Monitor real-time Vicon plug-in. Club head speed will be assessed utilizing a Tracman 4 dual radar tracking system.

Power output for participants will be measured by performing a countermovement vertical jump and a static vertical jump on the 4 Bertec non-conductive forceplate system.

Strength assessments will be performed in the Nimocks Fitness Center by the Lead Investigator. Maximal strength will be assessed in the following lifts utilizing the parameters described by the National Strength and Conditioning Association (4): Back Squat; Flat Bench Press. Other maximal strength numbers for primary lifts involved in the program (Front Squat; Incline Bench; Power Cleans) will be prescribed as percentages of the tested lifts as follows: Maximal Front Squat = 80% of Maximal Back Squat; Maximal Incline Bench = 80% of Maximal Flat Bench; Maximal Power Clean = 70% of Maximal Back Squat.

Study Type

Interventional

Enrollment (Anticipated)

16

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 Contact

Study Contact Backup

Study Locations

    • North Carolina
      • Fayetteville, North Carolina, United States, 28311

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria: college aged golfers with no contraindications to exercise as measured by PAR-Q+

  • No history of Heart condition or uncontrolled hypertension
  • No history of chest pain at rest or with exertion
  • No history of loss of balance or dizziness at rest or with exercise in previous 12 months
  • No medications for chronic medical conditions
  • No bone, joint, or soft tissue issue that could be made worse by becoming more physically active

Exclusion Criteria: As indicated by PAR-Q+

  • History of arthritis, osteoporosis, or chronic back issues
  • Current, or recent history of, cancer
  • Diagnosed cardiovascular disease: CAD, heart failure, diagnosed abnormality of heart rhythm
  • Uncontrolled high blood pressure (resting blood pressure of 160/90 or greater)
  • Diagnosed Metabolic Condition: Type 1 diabetes, Type 2 diabetes, Pre-diabetic

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Standard Periodization Training
Utilization of traditional periodization strength training model
Standard barbell resistance training programs
Active Comparator: Conjugate Training
Utilization of conjugate strength model
Standard barbell resistance training programs

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Gold club head speed and radar predicted 5-iron distance
Time Frame: 12 weeks
Trackman measured club head speed and predicted carry of 5 iron
12 weeks
Biomechanics of golf swing
Time Frame: 12 weeks
Bonita 16 camera measured biomechanical swing analysis
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Blake Justice, Methodist University

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 10, 2018

Primary Completion (Anticipated)

May 5, 2020

Study Completion (Anticipated)

May 5, 2020

Study Registration Dates

First Submitted

June 28, 2019

First Submitted That Met QC Criteria

June 28, 2019

First Posted (Actual)

July 2, 2019

Study Record Updates

Last Update Posted (Actual)

August 19, 2019

Last Update Submitted That Met QC Criteria

August 16, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • Project 2018 - 19 0027

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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