このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Effects of Dynamic Neuromuscular Stabilization (DNS) and Gyrotonic Training on Shoulder Function in Overhead Athletes (DNSGyroSHOA)

2026年4月30日 更新者:Jonida Drizaj、Sport University of Tirana

Evaluation of Effects of Dynamic Neuromuscular Stabilization Treatments and Other Innovative Methods on Shoulder Problems in Athletes

The goal of this randomized control trial is to evaluate the effect of the Dynamic Neuromuscular Stabilization (DNS) and Gyrotonic training compared to a control group on pain level, functional performance, and shoulder stability in overhead athletes aged 18 to 25 years. The main question is whether these interventions are more effective than usual training in improving clinical and performance related outcomes.

Participants will take part in a supervised rehabilitation program based on these methods three times per week for six weeks.

Assessments were performed at baseline and after 6 weeks of intervention. Outcome measures included pain level, functional performance, and dynamic shoulder stability. Also, core endurance, shoulder mobility, and shoulder muscle strength will be evaluated as a secondary outcomes.

These outcomes will be assessed using Visual Analog Scale (VAS), Kerlan-Jobe Orthopedic Clinic score (KJOC), the Y-Balance Upper Quarter Stability Test (UQYBT), McGill Endurance Test Battery, goniometer and digital dynamometer.

The study was approved by the Ethics Committee of the Sports University of Tirana. All participants involved in this study provided written informed consent.

調査の概要

詳細な説明

One of the most challenging aspects of orthopedic sports medicine is the rehabilitation of the overhead athletes. Overhead athletes place a lot of load on the shoulder joint, because of the volume of throws, mechanical stress and repetitive movements above shoulder level. During the game these athletes require high levels of mobility and stability at the same time, and neuromuscular control. Rapid motion, poor biomechanics, and weak links in the kinetic chain put this area in high risk of injury in glenohumeral joint and surrounding soft tissues. As a result, those athletes are exposed of developing shoulder pain, functional impairments, overuse injuries, and deficits in strength and mobility.

Recent rehabilitation programs for shoulder injuries in overhead athletes incorporate exercise-based interventions that integrate core activation, coordinated movement, and sport-specific function.

The purpose of this randomized controlled trial was to investigate the effect of structured neuromuscular rehabilitation program based on the Dynamic Neuromuscular Stabilization (DNS) method and Gyrotonic training on shoulder pain, functional performance, and dynamic stability in overhead athletes with shoulder injuries. The study looked for to determine whether these interventions could lead to significant improvements in the variables at baseline and after the interventions.

Participants meeting the inclusion criteria were recruited and were randomly allocated into one of three study groups. The intervention consisted of a supervised rehabilitation program focused on key components of shoulder function, such as neuromuscular control, strength, mobility, and coordination. The DNS program was focused on exercise based on developmental kinesiology, aimed to improve core stability, breathing patterns, and shoulder stabilization in various functional positions. The Gyrotonic program incorporated three-dimensional, spiral movement patterns aimed to improve mobility, coordination, and integrated upper limb function. The athletes involved in the DNS and Gyrotonic group continued also with their usual sports training. Exercise sessions were performed regularly in both intervention groups for a period of six-weeks. Participants in the control group continued with the usual training regime and did not receive any specific rehabilitation intervention.

Outcome assessments were conducted at baseline and after six weeks of intervention. Pain intensity, functional performance, dynamic stability were the main outcomes that were evaluated before and after the intervention period.

In addition, core endurance, mobility and muscle strength of glenohumeral joint was evaluated as a secondary outcome before and after the rehabilitation program. This study design allows the comparison of changes over time within and between groups in order to identify the most effective approach for improving pain, functional performance and stability in overhead athletes with shoulder injuries.

The findings of this study aim to provide clinically relevant evidence for the rehabilitation of overhead athletes with shoulder injuries.

研究の種類

介入

入学 (実際)

90

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Tirana
      • Tirana、Tirana、アルバニア、1001
        • Sport University of Tirana

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Male and female participants
  • Had a minimum of two years of sports experience
  • Presence of shoulder region injury or pain
  • Active participation in sports

Exclusion Criteria:

  • Shoulder surgery
  • Neurological disorders that can affect the upper limb
  • Shoulder dislocation
  • Orthopedic condition such as upper or lower limb fractures
  • Athletes with less than two years of sports experience

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:DNS Group
Participants involved in DNS group underwent a structured exercise-based intervention aimed to improve mobility, strength, and neuromuscular control. Also, the participants in this group followed the usual training program.
Dynamic Neuromuscular Stabilization (DNS) The exercise program based on the DNS method was focused on core activation, diaphragmatic breathing, and shoulder stabilization in various positions based on development kinesiology. Sessions were supervised by certificated therapist and were performed three times per week over a period of 6 weeks.
実験的:Gyrotonic Training Group
Participants in the Gyrotonic group followed an exercise program based on three-dimensional, flowing movement aimed to improve mobility, strength, and neuromuscular control. Also, the participants continued the usual training program.
A structured rehabilitation program based on the Gyrotonic method were conducted in the second intervention group. Sessions were supervised by certificated therapist and were conducted three times per week for 6 weeks. The program based on this method was focused on shoulder mobility and stability.
アクティブコンパレータ:Control Group
Participants included in control group continued their usual sports training routines without additional intervention during the study period.
Participants continued their usual sports training without any additional protocol exercise. The inclusion of the control group allows for the assessment of the additional effect of the interventions beyond usual training.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change from baseline in Shoulder Functional Performance (Kerlan-Jobe Orthopaedic Clinic Shoulder and Elbow Score)
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention
Shoulder functional performance was assessed using the Kerlan-Jobe Orthopedic Clinic Shoulder and Elbow Score Questionnaire (KJOC), a validated 0-100 scale, where higher scores indicate better function. Changes from baseline to post-intervention will be evaluated.
Baseline (pre-intervention) and after 6 weeks of intervention
Change from baseline in Shoulder Pain (Visual Analog Scale)
時間枠:Baseline (pre-intervention) and 6 weeks after of intervention.
Shoulder pain was assessed by Visual Analog Scale (VAS), a 0-10 scale, where higher scores indicate greater pain intensity. Changes from baseline to post-intervention will be evaluated.
Baseline (pre-intervention) and 6 weeks after of intervention.

二次結果の測定

結果測定
メジャーの説明
時間枠
Changes from baseline in Upper Limb Dynamic Stability (Upper Quarter Y Balance Test)
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Upper limb dynamic stability was assessed by Upper Quarter Y Balance Test (UQYBT), which evaluates reach distance in multiple directions to assess functional shoulder stability. Results were recorded in centimeters and normalized as a percentage of limb length. Higher scores indicates better dynamic stability.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Trunk Flexor Endurance
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Trunk flexor endurance was assessed using the McGill Endurance Battery Test and was recorded in seconds (s). Higher values indicate greater endurance
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Trunk Extensor Endurance
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Trunk extensor endurance was assessed by McGill Endurance Battery Test, a validated clinical assessment of trunk muscle endurance. Performance is recorded in seconds. Higher values indicate greater muscular endurance.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Shoulder Abduction Range of Motion
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Glenohumeral abduction range of motion (ROM) was assessed in both upper limbs, the dominant and non-dominant using a universal goniometer in degrees (◦). Goniometer is a validated instrument for joint angle measurement. Higher values indicate greater joint mobility. Changes from baseline to post intervention will be analyzed.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Shoulder Internal Rotation Range of Motion
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Glenohumeral internal rotation range of motion (ROM) was assessed in both upper limbs, the dominant and non-dominant using a universal goniometer in degrees (◦). Goniometer is a validated instrument for joint angle measurement. Higher values indicate greater joint mobility. Changes from baseline to post intervention will be analyzed.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Shoulder External Rotation Range of Motion
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Glenohumeral external rotation range of motion (ROM) was assessed in both upper limbs, the dominant and non-dominant using a universal goniometer in degrees (◦). Goniometer is a validated instrument for joint angle measurement. Higher values indicate greater joint mobility. Changes from baseline to post intervention will be analyzed.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Shoulder Internal Rotation Muscle Strength
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Shoulder internal rotation muscle strength was assessed using a digital dynamometer, a valid and reliable instrument for isometric muscle strength, and expressed in Newton (N). Higher values indicate greater muscle strength.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Shoulder External Rotation Muscle Strength
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Shoulder external rotation muscle strength was assessed using a digital dynamometer, a valid and reliable instrument for isometric muscle strength, and expressed in Newton (N). Higher values indicate greater muscle strength.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Shoulder Abduction Muscle Strength
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Shoulder abduction muscle strength was assessed using a digital dynamometer, a valid and reliable instrument for isometric muscle strength, and expressed in Newton (N). Higher values indicate greater muscle strength.
Baseline (pre-intervention) and after 6 weeks of intervention.

その他の成果指標

結果測定
メジャーの説明
時間枠
Change from baseline in Limb Symmetry Index
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Limb symmetry Index (LSI) will be calculated as the ratio of lower performing limb to higher performing limb, multiplied by 100 and expressed as a percentage(%). Values closer to 100% indicate greater inter-limb symmetry.
Baseline (pre-intervention) and after 6 weeks of intervention.
Changes from baseline in Glenohumeral Internal Rotation Deficit (GIRD)
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
Glenohumeral Internal Rotation Deficit (GIRD) will be calculate as the difference in shoulder internal rotation range of motion between the dominant and non-dominant shoulders, measured in degrees (◦). Higher values indicate greater internal rotation deficit.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in shoulder External to Internal Rotation Strength Ratio
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
The external/internal rotation (ER/IR) strength ratio will be calculated as the ratio of isometric external rotation strength to internal rotation strength measured using a digital dynamometer. The ER/IR ratio is unitless, with values of approximately 0.66-0.75 considered normal; values below 0.66 indicate external rotator strength deficit, while values above 0.75 indicate relative external rotator dominance or adaptation.
Baseline (pre-intervention) and after 6 weeks of intervention.
Change from baseline in Trunk Flexor to Extensor Endurance Ratio
時間枠:Baseline (pre-intervention) and after 6 weeks of intervention.
The trunk flexor/extensor endurance ratio will be calculated as flexor endurance time divided by extensor endurance time. The ratio is unitless, with values closer to 1 indicating better muscular balance.
Baseline (pre-intervention) and after 6 weeks of intervention.

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2025年2月17日

一次修了 (実際)

2025年3月17日

研究の完了 (実際)

2025年6月20日

試験登録日

最初に提出

2026年4月23日

QC基準を満たした最初の提出物

2026年4月30日

最初の投稿 (実際)

2026年5月7日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月7日

QC基準を満たした最後の更新が送信されました

2026年4月30日

最終確認日

2026年4月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

The individual participant data (IPD) will not be shared in order to protect participant confidentiality and privacy. In accordance with institutional regulations and informed consent obtained from participants, only overall results will be reported in publications.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する