Leg Muscle Activity Measured Via Electromyography in Back Squat Variations

NCT ID: NCT03902730

Last Updated: 2021-09-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

7 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-01

Study Completion Date

2021-09-25

Brief Summary

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The purpose of the study is to see how different forms of the squat exercise change my body's leg muscle activity. Four forms of the traditional back squat will be used: traditional back squat, barefoot squat, box squat, and traditional back squat with chains.

Detailed Description

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Resistance exercise has various benefits that promote health and reduce the chance of chronic disease, but the biggest benefit may be found in the effects on maintaining muscle mass throughout the aging process. The implications resistance training has on an individual's ability to function throughout the day with less fatigue whilst performing tasks at an easier level can all be related to improved strength and endurance that comes with resistance training. Furthermore, how the nervous system adapts and sends signals to the working muscles are of great interest as neuromuscular adaptations help in coordination, balance, and agility. Variations of the same style of exercise have been theorized to improve and/or change the adaptations that can occur. Thus, the purpose of this study would be to assess surface electromyography (sEMG) activations on 4 anatomical sites simultaneously during the squat exercise under varying conditions.

Conditions

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Surface Electromyography Muscular Fatigue

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Participants will complete all four trials in a crossover design. A one week washout period is required between treatments.
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants
Investigators will randomize treatments for all participants.

Study Groups

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Back Squat Variation One

In a randomized order, traditional back squat will be completed.

Group Type OTHER

Traditional Back Squat

Intervention Type OTHER

Participants will complete traditional back squat in this four treatment crossover design.

Back Squat Variation Two

In a randomized order, barefoot back squat will be completed.

Group Type OTHER

Barefoot Back Squat

Intervention Type OTHER

Participants will complete barefoot back squat in this four treatment crossover design.

Back Squat Variation Three

In a randomized order, box squat will be completed.

Group Type OTHER

Box Squat

Intervention Type OTHER

Participants will complete box squat in this four treatment crossover design.

Back Squat Variation Four

In a randomized order, traditional back squat with chains will be completed.

Group Type OTHER

Traditional Back Squat with Chains

Intervention Type OTHER

Participants will complete traditional back squat with chains in this four treatment crossover design.

Interventions

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Traditional Back Squat

Participants will complete traditional back squat in this four treatment crossover design.

Intervention Type OTHER

Barefoot Back Squat

Participants will complete barefoot back squat in this four treatment crossover design.

Intervention Type OTHER

Box Squat

Participants will complete box squat in this four treatment crossover design.

Intervention Type OTHER

Traditional Back Squat with Chains

Participants will complete traditional back squat with chains in this four treatment crossover design.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Participants will be males and females between the ages of 18 - 30 years
* Participant has provided written and dated informed consent to participate
* Participant is willing and able to comply with the protocol
* Participant is apparently healthy and free from disease, as determined by a health history questionnaire
* Participant agrees to abstain from lower body exercise 3 days prior to each testing visit
* Participant has completed at least 1 lower body workout every week for the past 6 months

Exclusion Criteria

* Participant reports any unusual adverse events associated with this study that in consultation with their physician recommends removal from the study
* Participant begins consumption of new supplement during the timeline of this study
* Participant is unable to refrain from consuming pre-workout supplement prior to testing sessions
* Participant is unwilling to refrain from lower body exercise at least 3 days prior to each testing session
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Mary Hardin-Baylor

OTHER

Sponsor Role lead

Responsible Party

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Lemuel W. Taylor IV

Director of Research in HPL

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Lemuel W Taylor IV, PhD

Role: PRINCIPAL_INVESTIGATOR

UMHB Human Performance Lab

Locations

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UMHB Human Performance Lab

Belton, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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EMG-1

Identifier Type: -

Identifier Source: org_study_id

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