- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05317299
Comparison of the Effects of Different Exercise Types
Comparison of the Effects of Different Exercise Types on Lower Extremity Muscle Thickness, Tendon Thickness, Muscle Strength, Proprioception and Balance
Study Overview
Detailed Description
The choice of exercise type is affected by many different factors. The purpose of exercise and the physical fitness parameter they want to develop gain importance in this choice.
Resistance exercises (RE) specifically designed to increase muscle strength and hypertrophy; Plyometric exercises (PE) based on energy storage of the muscle during the deceleration phase and release of this energy during the acceleration period and high-intensity interval training (HIIT), which is an advanced form of interval training that includes shorter and lighter recovery periods following short to heavy anaerobic exercise are some of the many types of exercises in the literature and practice.
The purpose of the study is investigate the comparison of the effects of different exercise types on lower extremity muscle thickness, tendon thickness, muscle strength, proprioception and balance.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Muğla, Turkey, 48000
- Muğla Sıtkı Koçman University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being 18-30 years old
- Being a man
- Volunteering to participate in the study
- Having a normal BMI (18.5-24.9) according to the World Health Organization criteria
Exclusion Criteria:
- Having any physical, mental or psychological illness that may affect participation in the study
- Having a history of trauma to the lower extremity requiring medical, conservative and surgical treatment in the last 6 months
- Consuming alcohol or pharmaceuticals up to 24 hours before the assessment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Resistance Exercise Group
During 8 week progressive resistance exercises (three times a week)
|
Group 1: Resistance Exercise Group 2: Plyometric Exercise Group 3: Hight Intensity Interval Training
|
Active Comparator: Plyometric Exercise Group
During 8 week progressive plyometric exercises (three times a week)
|
Group 1: Resistance Exercise Group 2: Plyometric Exercise Group 3: Hight Intensity Interval Training
|
Active Comparator: High Intensity Interval Training Group
During 8 week progressive Hight Intensity Interval Training (three times a week)
|
Group 1: Resistance Exercise Group 2: Plyometric Exercise Group 3: Hight Intensity Interval Training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle Thickness assessment with B-mode Ultrasonography
Time Frame: 8 weeks
|
Changes of lower extremity muscle thickness
|
8 weeks
|
Tendon Thickness assessment with B-mode Ultrasonography
Time Frame: 8 weeks
|
Changes of lower extremity tendon thickness
|
8 weeks
|
Muscle Strength assessment with manual dinamometer
Time Frame: 8 weeks
|
Changes of lower extremity muscle strength
|
8 weeks
|
Joint position sense assessment with angle repetition test
Time Frame: 8 weeks
|
Changes of lower extremity joint position sense
|
8 weeks
|
a kinesthetic ability trainer (Sport KAT Model 650-TS)
Time Frame: 8 weeks
|
Changes of static and dynamic balance
|
8 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
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
- 220023/30
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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