the Effect of Stabilization on Archery Performance

NCT06126458 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2023-11-13

No results posted yet for this study

Summary

The aim of this study was to investigate the effect of stabilization and stabilization-related parameters on shooting performance at the cervical, lumbal and scapular levels in archery athletes. A total of 40 archery athletes aged between 10 and 18, who have been professionally engaged in archery for at least 1 year were included in the study. Demographic information and musculoskeletal system evaluations of the athletes were done. Performance of the athletes via Upper Extremity Closed Kinetic Chain Stability Test, Hand Grip Strength test; presence of scapular dyskinesia was evaluated via the Lateral Scapular Slide Test. Cervical region stabilization was evaluated via Craniocervical Flexion Test, scapular level stabilization was evaluated via Scapular Muscle Endurance Test, lumbar region stabilization was evaluated via Abdominal Drawing-in Test and Sahrmann's Core Stability Test. As the parameters related to stabilization, postures via Corbin Postural Rating Scale; balances via Stork Balance Test, Upper Extremity Y Balance Test; pain was evaluated via the Shoulder Pain and Disability Index. Shooting performances were evaluated with 72 target shootings and a total of 720 points. .

Conditions

  • Athletic Injuries
  • Instability, Joint

Interventions

OTHER

shooting performance

collecting total points after 72 target shootings done

Sponsors & Collaborators

  • Aynur Demirel

    lead OTHER

Principal Investigators

  • Aynur Demirel, Assoc. Prof. · Hacettepe University

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-11-05
Primary Completion
2022-11-06
Completion
2022-11-06

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06126458 on ClinicalTrials.gov