Muscle Activations During Bulgarian Split Squat Exercise Variations

December 1, 2023 updated by: Elif AYGUN POLAT

Effect of Trunk Position on Muscle Activations During Traditional and Suspension Based Bulgarian Split Squat

It is essential to practice and train appropriate activation techniques to ensure optimum strength development. Knowing the effects of exercise variations that will minimize the tension forces acting on the knee by increasing the activation of the lumbo-pelvic-hip complex muscles, which are critical during sports activities, is extremely important in terms of preventing injuries. The aim of this study is to compare muscular activations during traditional and suspension-based Bulgarian split squat exercises and to examine the effect of trunk position on muscular activations.

Study Overview

Status

Completed

Detailed Description

This study utilized a single-group repeated-measures design, where 4 conditions-Bugarian split squat with trunk flexion (BSS flexion), Bulgarian Split squat with trunk neutral (BSS neutral), suspension based Bulgarian split squat with trunk flexion (SBSS flexion), suspension based Bulgarian split squat with trunk neutral (SBSS neutral)-were examined.Participants had to make two separate trips to the lab in order to be accepted into the study. All exercises were introduced to participants at the initial visit. Prior to beginning the exercises on the second visit, the participants' maximum voluntary isometric contraction (MVIC) values were calculated. The muscle activity of the gluteus medius (GMed), gluteus maximus (GMax), vastus lateralis (VL), rectus femoris (RF), vastus medialis (VM), semitendinosus (ST), biceps femoris (BF),and erector spina (ES) was monitored through the root mean square surface EMG signal amplitude. The order of the tasks was chosen for each person by straightforward randomization (by selecting from a deck of shuffled cards) so order to reduce the impact of the sequence of the exercises.The modified Borg scale was used to ensure that fatigue did not occur before each exercise since it was believed that fatigue could affect exercise performance.

Study Type

Interventional

Enrollment (Actual)

21

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

      • Ordu, Turkey, 52200
        • Ordu University

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Being a licensed athlete in one's own field,
  • Having been engaged in sports for at least 2 years

Exclusion Criteria:

  • Individuals with any musculoskeletal injury history in the lower extremities and trunk that could impede exercise within the last year,
  • Individuals with systemic, neurological, and/or cognitive issues,
  • Individuals experiencing pain in the lower extremities and trunk during exercises

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: Diagnostic
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: female athletes
21 female athletes from different branches performed 4 different sessions of Bulgarian split squat exercises.
The participants performed 4 different sessions of Bulgarian split squat exercises-Bulgarian split squat with trunk flexion (BSS flexion), Bulgarian Split squat with trunk neutral (BSS neutral), suspension based Bulgarian split squat with trunk flexion (SBSS flexion), suspension based Bulgarian split squat with trunk neutral (SBSS neutral)-with EMG recordings being taken from the dominant extremity throughout each session. For each exercise, participants were instructed to perform three successful repetitions. Between each repetition, there was a 30-second break, and there was at least 10 minutes in between each of the 4 exercises. The movement was standardized by a metronome. The modified Borg scale was used to ensure that fatigue did not occur before each exercise since it was believed that fatigue could affect exercise performance. When scores reported using the modified Borg scale were 1 or lower, exercise recording was started.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Surface EMG Measurement
Time Frame: in an average of one hour
During data collection, the EMG Noraxon MiniDTS system (Noraxon Inc.) was used to measure the signals from the muscle. Additionally, the participants were video-recorded to prevent any potential mistakes that might have gone unnoticed during the activities.
in an average of one hour
Normalization of Surface EMG
Time Frame: in an average of one hour

To normalize the EMG data obtained during the exercises, MVIC was performed for each muscle.

Participants were asked to warm up on a treadmill at submaximal speed for 8 minutes before starting the measurements. Measurements were performed with 3 repetitions, each lasting 5 seconds, and a 1-minute rest period between repetitions. During the measurements, participants were verbally encouraged to give their maximum effort. After the MVIC measurements, participants were given a 5-minute rest period.

in an average of one hour

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Elif AYGUN POLAT, T.C. ORDU ÜNİVERSİTESİ
  • Study Director: Nevin A. GUZEL, Gazi University
  • Principal Investigator: Sonay GURUHAN, Gazi University
  • Principal Investigator: Nihan KAFA, Gazi 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)

July 1, 2022

Primary Completion (Actual)

September 1, 2022

Study Completion (Actual)

May 30, 2023

Study Registration Dates

First Submitted

October 19, 2023

First Submitted That Met QC Criteria

October 26, 2023

First Posted (Actual)

November 1, 2023

Study Record Updates

Last Update Posted (Estimated)

December 8, 2023

Last Update Submitted That Met QC Criteria

December 1, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • ODU-SBFTR-AYGUNPOLAT

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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