- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05623657
Comparison of the Efficiency of Game-Based Exercise Program and Trunk Stabilization Exercise Training in Adolescent Playing Archery
Game-Based Exercise Program and Trunk Stabilization Exercise Training in Adolescent Playing Archery
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Istanbul, Turkey
- Istanbul University-Cerrahpasa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Archers who have been practicing archery for at least 1 year
- Roller or Olympic archers
Exclusion Criteria:
- Archers with a history of musculoskeletal injuries causing physical limitation in the last 6 months.
- Archers who did not volunteer to participate in the study.
- Archers with any visual and hearing disabilities.
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 |
|---|---|
|
Experimental: Trunk Stabilization Exercise Training Group
|
The adolescents in this group who are involved in archery sports will be given 40 minutes of exercise training 2 days a week for 8 weeks.
Exercise training will be applied as 5-10 minutes warm-up, 15-30 minutes trunk stabilization exercises, 5-10 minutes cooling down, and stretching exercises.
The number of repetitions and difficulty levels of the exercises will gradually increase in the 3rd and 6th weeks.
|
|
Experimental: Game Based Exercise Program Group
|
At least 4 different games selected from Xbox 360 Kinect® games will be applied to adolescents practicing archery sports in this group for a total of 40 minutes with the physiotherapist.
The games will be selected from games that include movement patterns similar to the exercises of the trunk stabilization exercise group.
Game-based exercise training is planned to be performed twice a week for a total of 8 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Core Endurance Tests
Time Frame: Change from baseline to 8 weeks
|
McGill's tests will be used to examine participants' core endurance.
These tests consist of four positions: the trunk anterior flexor test, the right and left lateral plank, and the trunk posterior extensor test.
Participants will perform one practice trial that will last a few seconds to confirm position and then one actual test trial will be recorded per position where the maximum time (seconds) participants could hold a static position was measured.
The same investigator visually will determine the end of all tests.
|
Change from baseline to 8 weeks
|
|
Star Excursion Balance Test (SEBT) :
Time Frame: Change from baseline to 8 weeks
|
The test requires strength, flexibility, and proprioception.
It is a measure of dynamic balance that provides a significant challenge to athletes and physically active individuals.
The participant performing the test must maintain their balance on one leg while using the other leg to reach as far as possible in 8 different directions.
The participant (standing on his/her left leg for example) must reach in 8 different positions, once in each of the following directions: anterior, anteromedial, medial, posteromedial, posterior, posterolateral, lateral and anterolateral.
The anterior, posteromedial and posterolateral directions appear to be important to identify individuals with chronic ankle instability and athletes at greater risk of lower extremity injury.
|
Change from baseline to 8 weeks
|
|
Reaction Time Evaluation:
Time Frame: Change from baseline to 8 weeks
|
It plans to use the free platform game (Reaction Time) available in the Android app. Test The test is performed using a tablet in a quiet and lighted room, the tablet will be placed on the desktop with a stabilizing stand.Athletes participating in the study will be asked to sit in a chair so that they are comfortable on the table.Test protocols after a verbal explanation, the athletes will be given one trial before the reaction time measurement. Stimuli given 5 times at fixed and random intervals, the average of the 5 trials results in the reaction time in milliseconds. The participant is asked to touch the middle of the tablet screen with his finger when the blue color appears.When the green color appears, the screen continues to be touched, and when the green color appears, the screen is quickly stopped being touched. All athletes have a dominant and The non-dominant side uses the hands, index fingers. |
Change from baseline to 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shooting Performance Evaluation:
Time Frame: Change from baseline to 8 weeks
|
Outdoor Shooting Performance: A total of 72 arrows, 2 x 36 arrows, will be shot at the distances specified by the International Archery Federation.
The series were shot as 6 arrows each.
A total of 360 points will be calculated.
The higher the score, the better the performance of the athlete.
Each athlete used his/her own bow and arrow, and the athlete must complete the shots within certain time limits.
|
Change from baseline to 8 weeks
|
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
Keywords
Other Study ID Numbers
- 00001
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.
Clinical Trials on Athlete; Itch
-
University of Sao PauloCompletedItch; Athlete | Individual AdjustmentBrazil
-
University Hospital, Basel, SwitzerlandCompletedItch; AthleteSwitzerland
-
Beijing Sport UniversityWuhan Sports UniversityCompletedAthlete | Exercise Recovery | Sport Performance | Elite AthleteChina
-
Aalborg UniversityRecruiting
-
Aalborg UniversityNot yet recruiting
-
Istanbul Medipol University HospitalCompleted
-
National Taiwan Sport UniversityUnknown
-
Universidade Federal de Sao CarlosFundação de Amparo à Pesquisa do Estado de São Paulo; Centro de Pequisas de...Completed
-
University Hospital, Basel, SwitzerlandCompleted
Clinical Trials on Trunk Stabilization Exercise Training Group
-
University of VermontEunice Kennedy Shriver National Institute of Child Health and Human Development...Completed
-
University of Social Welfare and Rehabilitation...CompletedLow Back PainIran, Islamic Republic of
-
lee kyoungjuCompletedLow Back Pain | Breathing Exercise | Core StabilitySouth Korea
-
Khon Kaen UniversityCompleted
-
Inje UniversityUnknown
-
Bundang CHA HospitalNot yet recruiting
-
Dow University of Health SciencesCompletedOsteoarthritis, KneePakistan
-
Başakşehir Çam & Sakura City HospitalActive, not recruitingStrokeTurkey (Türkiye)
-
Superior UniversityActive, not recruiting