- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06001242
The Relationship Between Upper Extremity Explosive Power and Trunk Muscles in Volleyball Players
October 12, 2023 updated by: Aynur Demirel, Hacettepe University
Voleybolcularda Üst Ekstremite Patlayıcı Güç Ile Gövde Kaslarının Arasındaki İlişkinin İncelenmesi
Volleyball is an interval sport involving consecutive aerobic and anaerobic loads.
Strength training based on explosive movements can improve performance in the upper extremities.
Strength performance has an important place in this sport.
Trunk stabilization is defined as 'proximal stability for distal mobility'.
Disorder in any segment of the kinetic chain model will affect the quality of movement in the lower and upper segments.The aim of this study is to examine the relationship between the morphological features of the transversus abdominis, lumbal multifidus (L4-5), internal external oblique muscles, and the anaerobic power of the upper extremity and shoulder girdle functionThis study was designed as a cross-sectional.
They will consist of 30 volleyball players between 14-30 years of age.
Muscle morphological features of the participants by ultrasound; explosive strength will be evaluated by Medicine Ball Throw test, functional evaluation will be evaluated by Closed Kinetic Chain Upper Extremity Endurance test.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Aynur Demirel
- Phone Number: +90 305 157 6168
- Email: aynur.demirel@hacettepe.edu.tr
Study Contact Backup
- Name: Merve Çömlekçi
- Phone Number: +905063355195
- Email: comlekcimerve@gmail.com
Study Locations
-
-
-
Ankara, Turkey, 06100
- Aynur Demirel
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Hacettepe University will be directed from the referred athletes
Description
Inclusion Criteria:
- Training for an hour at least 3 days a week for at least 1 year
- Body Mass Index (BMI) below 30 kg/m2
- No concomitant neurological, rheumatological or systemic disease
- Volunteer to participate in the study.
Exclusion Criteria:
- Having any surgery / serious pathology of the spinal column
- Having had an upper extremity injury in the last 6 months that would affect his ability to play volleyball
- Having an injury that requires at least 2 weeks of discontinuation
- Severe musculoskeletal/systemic discomfort during the measurements.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle morphology
Time Frame: 1 day
|
Morphological characteristics transverse abdominis, lumbar multifidus,internal obliquus, external obliquus will be evaluated via ultrasound imaging
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Expolsive Power
Time Frame: 1 day
|
Medicine Ball Throw
|
1 day
|
Core stability
Time Frame: 1 day
|
Sharmannn's Core Stability Test
|
1 day
|
Upper Extremity Endurance
Time Frame: 1 day
|
Closed Kinetic Chain Upper Extremity Stability Test
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Aynur Demirel, PhD, HACETTEPE UNIVERSİTY
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 (Estimated)
October 26, 2023
Primary Completion (Estimated)
August 26, 2025
Study Completion (Estimated)
August 26, 2025
Study Registration Dates
First Submitted
August 14, 2023
First Submitted That Met QC Criteria
August 18, 2023
First Posted (Actual)
August 21, 2023
Study Record Updates
Last Update Posted (Actual)
October 13, 2023
Last Update Submitted That Met QC Criteria
October 12, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- GO 23/540
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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