- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06112015
Muscle Activations During Bulgarian Split Squat Exercise Variations
Effect of Trunk Position on Muscle Activations During Traditional and Suspension Based Bulgarian Split Squat
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Ordu, Turkey, 52200
- Ordu University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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.
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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.
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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.
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in an average of one hour
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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
Sponsor
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
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- ODU-SBFTR-AYGUNPOLAT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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