- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05261789
Comparison of the Effects of Turkish Get Up Exercise and Stabilization Exercises on Muscular Activation, Core Stability and Upper Extremity Performance in Healthy Individuals
Turkish Get Up (TGU) exercise, which is one of the kettlebell exercises, is a multi-step, progression-based, functional and whole-body exercise method that includes a combination of movements such as lunge, bridge building and side plank. Strength training, dynamic flexibility exercises and strength training can be performed with the use of a kettlebell. Exercises with a kettlebell are frequently used in the fields of improving sportive performance and rehabilitation. TGU exercise can be used as a corrective exercise as well as in motion analysis and conditioning studies. TGU exercise consists of 2 stages:The first stage is performed in seven different steps: 1. Starting position, 2. Supine kettlebell lift, 3. Elbow-supported kettlebell lift, 4. Hand-supported kettlebell lift, 5. High bridge, 6. Half-kneeling and lunge position, 7. Stand up. In the second stage, the exercise is completed by performing the return of the steps in the first stage. It is thought that the deltoid, rectus abdominis, external oblique abdominis, erector spinae, gluteal muscles, quadriceps and hamstring muscles are activated during this exercise. It has been reported that with the TGU exercise, especially rotator cuff muscle strength, shoulder stability, balance and core stability can be improved.
In the literature, there are many studies examining the effects of stabilization exercises on core muscles. On the other hand, although there are studies reporting that the TGU exercise can improve core stability and shoulder stability, and studies reporting the muscular activation of the shoulder girdle muscles and some trunk muscles during the TGU exercise. To the best of our knowledge, we have not found a study examining its effectiveness on muscle activation, core stability and upper extremity performance and comparing it with any other method.
The aim of this study is to compare the effects of TGU exercise and stabilization exercises on muscular activation, core stability and upper extremity performance in healthy individuals.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Ankara, Turkey
- Ankara Yildirim Beyazit University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy, male individuals, between the ages of 18-25, Individuals whose physical activity levels are at least 3000 MET min/week and above according to the International Physical Activity Questionnaire-Short Form, Individuals with a body mass index of 17-30 kg/m2
Exclusion Criteria:
- Professionally engaged in sports, Have any known orthopedic, neurological or cardiovascular problems, Having undergone musculoskeletal surgery in the last 1 year, Individuals who have had a musculoskeletal injury in the last 3 months.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Turkish Get Up exercise group
Turkish Get Up exercise was given this group
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Before the exercise, warm-up exercises (low intensity aerobic activity, short-term stretches) were applied for 5 minutes. 7 different steps (1. Starting position, 2. Supine kettlebell lift, 3. Elbow-supported kettlebell lift, 4. Hand-supported kettlebell lift, 5. High bridge, 6. Half-kneeling and lunge position, 7. Standing up) and the return of these different steps, a total of 2 stages exercise program was applied. The exercise was started with 3 repetitions for each side and 3 sets with a 30-second rest period between repetitions, and 2 minutes of rest between sets. At the beginning of the 3rd week, the exercise was applied as 3 sets of 4 repetitions, and at the beginning of the 5th week, 3 sets of 5 repetitions were applied. At the end of the exercise, cool-down exercises (low intensity jogging and static stretching) were applied for 5 minutes. |
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Experimental: Core stability exercise group
Core stability exercise was given this group
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After the individuals were taught how to activate their core muscles before the exercise, they were asked to do bridge, prone and lateral bridge exercises by contracting their core muscles. Before the exercises, warm-up exercises (low intensity aerobic activity, short-term stretches) were applied for 5 minutes. Bridge exercise, prone bridge exercise, lateral bridge exercise were applied |
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Active Comparator: Control group
No intervention
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No exercise will be applied to the individuals in the control group.
At the end of the 6-week period, all parameters will be evaluated again.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Core stability
Time Frame: 6 weeks
|
Core stability of individuals, static endurance; were performed with trunk flexors endurance test, Measurement were recorded in seconds using a digital stopwatch.
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6 weeks
|
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Core stability
Time Frame: 6 weeks
|
Core stability of individuals, static endurance; were performed with trunk extensors endurance test, Measurement were recorded in seconds using a digital stopwatch.
|
6 weeks
|
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Core stability
Time Frame: 6 weeks
|
Core stability of individuals, static endurance; were performed with lateral bridge endurance test, Measurement were recorded in seconds using a digital stopwatch.
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6 weeks
|
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Core stability
Time Frame: 6 weeks
|
Core stability of individuals, static endurance; were performed with the prone bridge test, Measurement were recorded in seconds using a digital stopwatch.
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6 weeks
|
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Muscle activation
Time Frame: 6 weeks
|
Muscle activations of individuals were evaluated using superficial EMG.
An 8-channel EMG Noraxon MiniDTS system (Noraxon, USA, Inc, Scottsdale, AZ) was used to measure signals from the muscles.
Before placing the electrodes, the skin was prepared by shaving the area to be treated and cleaning with alcohol cotton until the skin was slightly red in order to reduce the skin impedance.
Electrodes, Surface It was placed parallel to the muscle fibers at the points recommended by ElectroMyoGraphy for the Non-Invasive Assessments of Muscles (SENIAM).
On the dominant side of individuals; Electrodes were placed 15 cm lateral to the umbilicus for external oblique abdominis, 2 cm above and 3 cm lateral to the umbilicus for rectus abdominis, and 3 cm lateral to the L3 spinous process for lumbar erector spinae.
|
6 weeks
|
|
Upper extremity performance
Time Frame: 6 weeks
|
The upper extremity Y balance test was used to evaluate the balance, function and stability of the upper extremity and trunk.
In the initial phase of the test, the individual took a push-up position with arms shoulder-width apart.
Before the test, the individual was allowed to try 3 times for warming up.
During the test phase, the nondominant hand was extended 3 times in the medial, inferior lateral and superior lateral directions, and the distance was recorded, and then the dominant hand was passed.
Composite score was obtained by dividing the total score of 3-repetition distance for each direction by 3 times the length of the upper extremity.
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6 weeks
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Collaborators and Investigators
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2019-168
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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