The Effects of Increased vs. Traditional Squat Stance Width on Performance Indices in Elite Rugby League Players

August 31, 2022 updated by: Jonathan Sinclair, University of Central Lancashire

The Effects of Increased vs. Traditional Squat Stance Width on Performance Indices in Elite Rugby League Players; an 8-week Pre-season Randomized Control Intervention

The back squat is a commonly utilized resistance training exercise for the promotion of both performance and musculoskeletal health. There are a range of manipulations that can be made to the setup of this resistance exercise, with once such adaptation being the stance width when performing the exercise. This intervention aims to explore the effects of increasing the stance with on performance indices in elite rugby league players.

Study Overview

Study Type

Interventional

Enrollment (Actual)

26

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

    • Lancashire
      • Preston, Lancashire, United Kingdom, PR4 0PE
        • University of Central Lancashire

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 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Rugby league player contracted to a professional Super League team
  • 5-years minimum of back squat experience
  • Male
  • Injury free for 6-months

Exclusion Criteria:

  • Female
  • Any injury at baseline
  • Any international matches played during the between season break

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Normal stance width
Those assigned to this group will complete their pre-season training as normal i.e. when performing their squat exercises they will do so using their habitual (self-selected) stance width.
Normal self-selected stance width when performing squat exercises.
Experimental: Wide stance width
Those assigned to this (i.e. experimental) group will also complete their pre-season training as normal, the only exception will be that when performing their squat exercises they will increase their stance width by 20% compared to their self-selected stance width.
Increased stance with (by 20% over their own self-selected stance width) when performing squat exercises.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
505 agility test
Time Frame: Baseline
Test of 180 degree turning ability, measured using timing gates.
Baseline
505 agility test
Time Frame: 8-weeks
Test of 180 degree turning ability, measured using timing gates.
8-weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body mass
Time Frame: Baseline
Body mass using a weighing scale.
Baseline
Body mass
Time Frame: 8-weeks
Body mass using a weighing scale.
8-weeks
Sum of skinfold thickness
Time Frame: Baseline
Skinfold thicknesses measured using callipers at eight sites according to the International Society for the Advancement of Kinanthropometry (ISAK) restricted profile (triceps, subscapular, biceps, iliac crest, supraspinal, abdominal, mid-thigh, and medial calf)
Baseline
Sum of skinfold thickness
Time Frame: 8-weeks
Skinfold thicknesses measured using callipers at eight sites according to the International Society for the Advancement of Kinanthropometry (ISAK) restricted profile (triceps, subscapular, biceps, iliac crest, supraspinal, abdominal, mid-thigh, and medial calf)
8-weeks
Three repetition maximum squat strength
Time Frame: Baseline
The maximum squat weight that can be lifted for a total of three repetitions
Baseline
Three repetition maximum squat strength
Time Frame: 8-weeks
The maximum squat weight that can be lifted for a total of three repetitions
8-weeks
Counter movement jump height
Time Frame: Baseline
The maximum height that can be jumped vertically, measured using a jump mat.
Baseline
Counter movement jump height
Time Frame: 8-weeks
The maximum height that can be jumped vertically, measured using a jump mat.
8-weeks

Collaborators and Investigators

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

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)

October 1, 2021

Primary Completion (Actual)

December 1, 2021

Study Completion (Actual)

April 1, 2022

Study Registration Dates

First Submitted

August 16, 2022

First Submitted That Met QC Criteria

August 16, 2022

First Posted (Actual)

August 18, 2022

Study Record Updates

Last Update Posted (Actual)

September 6, 2022

Last Update Submitted That Met QC Criteria

August 31, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • Squat stance width

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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