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OpenTrials
Completed

NCT Number: NCT03247777

Benefits of Traditional and Golf-specific Resistance Training in Amateur Female Golfers

Amateur female golfers were randomized to either a functional weight lifting group or a traditional weight lift group. Testing, consisting of performance measures and golf measures, was performed at baseline and after 10 weeks of weight lifting.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Human Biomechanics and Physiology Study

High Point, North Carolina, 27262, United States

About this study

A randomized control trial to compare the effects of 10 weeks of two different types of training in recreationally active female golfers was performed. Participants were recruited through postings at local country clubs and public golf courses, as well as through emails to state and local women's golf associations. Following written informed consent approved by the university's institutional review board, participants completed a medical and golf history questionnaire. Golf-specific information gathered via the history form included self-reported number of years playing golf, handicap, frequency of play, frequency of practice. Baseline testing followed, consisting of measurement of height and weight using a stadiometer, bone density and body composition using dual energy X-ray absorptiometry (DXA), 7-iron and driver club speed and total ball distance using a golf simulator (High Definition Golf, Interactive Sports Technologies, Vaughan, Ontario), and physical performance tests. Participants were then randomly assigned, using a random number generator, to either a traditional resistance training group (TRAD) or a golf-specific resistance training group (GSRT). Resistance training was conducted 3 days per week for 10 weeks. Each training session was directly supervised by at least one of the researchers, such that correct technique and appropriate resistance could be monitored. Following the 10 weeks of training, participants repeated the testing procedures under similar conditions as baseline testing.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • females ≥18 years of age,
  • and an official handicap or completion of at least 5 rounds of golf within the last year

Exclusion criteria

  • Exclusion criteria were current episode of musculoskeletal pain,
  • unable to stand and swing a golf club independently,
  • systemic disease including but not limited to rheumatologic disease or cancer,
  • or psychological or other cognitive impairment.

Treatment and study plan

Traditional strengthening

Other

dead lifts, bench press, wrist curls, and lat pulldowns as examples

Functional Strengthening

Other

diagonal chops, one leg deadlifts, lateral plyometrics as examples

Primary outcomes

  1. Driver club speed

    Time frame: 10 weeks

    Driver club speed- continuous variable measured in mph

  2. 7-iron club speed

    Time frame: 10 weeks

    7-iron club speed-continuous variable measured in mph

  3. Driver distance

    Time frame: 10 weeks

    Driver distance-continuous variable measured in yards

  4. 7-iron distance

    Time frame: 10 weeks

    7-iron -continuous variable measured in yards

Secondary outcomes

  1. Seated rotation flexibility

    Time frame: 10 weeks

    sit and rotate left and right- continuous variable measured with a goniometer in degrees

  2. Weighted ball golf toss

    Time frame: 10 weeks

    Using a golf-like motion, toss a 6lb ball as far as possible- continuous scale measured in cm

  3. Weighted ball seated toss

    Time frame: 10 weeks

    sitting in a declined position, use a chest pass motion to toss a 6 lb ball as far as possible- continuous measure measured in cm

Other outcomes

  1. Bone density

    Time frame: 10 weeks

    bone density- continuous measure measured using a dual image x-ray absorptiometry (DEXA) scan

  2. Body fat percentage

    Time frame: 10 weeks

    body fat percentage- 0-100% scale measured using a DEXA scan

Sponsors and collaborators

Lead sponsor

High Point University

Other

Registry information

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Aug 14, 2017
Registry last updated
Aug 14, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.