- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05505786
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
Status
Completed
Conditions
Intervention / Treatment
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.
Sponsor
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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