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Muscle Thickness, Trunk Proprioception, and Postural Stability in Rotator Cuff Pathology

2026年7月30日 更新者:Bilinç Doğruöz Karatekin、Istanbul Medeniyet University

Evaluation of the Relationship Between Latissimus Dorsi and Abdominal Muscle Thickness, Trunk Proprioception, and Postural Stability in Patients With Rotator Cuff Pathology

The rotator cuff consists of the supraspinatus, infraspinatus, teres minor, and subscapularis muscles and their tendons, which surround and stabilize the shoulder joint. Rotator cuff-related disorders may cause pain, particularly during arm elevation and external rotation, and may limit shoulder movement and daily function.

Shoulder function depends not only on the muscles surrounding the shoulder but also on the coordinated transfer of force through the trunk and extremities, known as the kinetic chain. Impairments in trunk muscle function, core stability, proprioception, and balance may therefore negatively affect shoulder mechanics.

This study aims to investigate the relationships between latissimus dorsi and abdominal muscle thickness, trunk proprioception, and postural stability in individuals with rotator cuff pathology. The study will also examine whether these measurements differ between individuals with rotator cuff pathology and healthy participants.

調査の概要

状態

募集

詳細な説明

The rotator cuff consists of the supraspinatus, infraspinatus, teres minor, and subscapularis muscles and their tendons and surrounds the shoulder joint. Rotator cuff syndrome includes various conditions affecting the rotator cuff, such as subacromial impingement syndrome, bursitis, tendinitis, and partial- or full-thickness rotator cuff tears. Rotator cuff-related shoulder pain generally refers to a painful clinical condition that occurs during shoulder elevation and external rotation and is accompanied by limitations in shoulder movement and function. Its etiology is multifactorial. The combination of extrinsic mechanical compression, such as narrowing of the subacromial space, and tendon overuse, such as repetitive overhead activities, has been identified as one of the main mechanisms underlying rotator cuff pathology. Diagnosis is based on medical history, physical examination, and imaging when necessary.

Sequential physiological muscle activations in the upper and lower extremities create an integrated biomechanical task. This sequential organization is referred to as the kinetic chain. During activities predominantly involving the upper extremity, energy is generated and transferred from the proximal to the distal segments. A disruption within the kinetic chain may result in dysfunctional biomechanical outcomes and contribute to the development of pain and injury. Impairments in the proximal components of the kinetic chain may negatively affect shoulder function. Therefore, in patients with shoulder disorders, all components that may impair kinetic chain function should be evaluated.

Core stability is defined as the ability to control the position and movement of the trunk over the pelvis in order to enable optimal force generation and the transfer and control of force and movement to the distal segment during activity. Core muscle activity provides both stability and movement. This mechanism enables proximal stability for distal mobility, the sequential transfer of force from proximal to distal segments, and the generation of intersegmental moments that move and protect the distal joints. The core region is important for providing local strength and balance. It is also positioned at the center of almost all kinetic chains involved in sporting activities. Therefore, adequate core muscle strength facilitates effective control of balance and movement and supports the optimal functioning of kinetic chains associated with both upper- and lower-extremity activities.

The sensorimotor system includes all sensory and motor components involved in maintaining joint stability, together with their central integration and processing mechanisms. This system consists of several components, including proprioception, joint position sense, kinesthesia, force sense, and neuromuscular control. When a shoulder injury occurs, not only mechanical structures such as the joint capsule and glenoid labrum may be affected, but the sensorimotor system may also be impaired. Shoulder injuries may be accompanied by deficits in both proprioception and neuromuscular control, which may consequently result in balance impairments.

Some studies have suggested that pain may also contribute to balance impairment. A possible explanation is that pain-processing mechanisms, the neuronal networks responsible for balance control, and pain-related muscle inhibition partly involve shared pathways within the central nervous system. A recent study conducted in Türkiye that investigated balance in patients with shoulder pain reported a significant difference in balance between the patient and control groups. The study also found that balance impairment was positively associated with pain severity.

This study aims to investigate the relationships between latissimus dorsi and abdominal muscle thickness, trunk proprioception, and postural stability in individuals with rotator cuff pathology. The study will also examine whether these measurements differ between individuals with rotator cuff pathology and healthy participants.

研究の種類

観察的

入学 (推定)

80

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。

研究連絡先

研究場所

    • Kadıköy
      • Istanbul、Kadıköy、トルコ(Türkiye)、34722
        • 募集
        • Göztepe Prof. Dr. Süleyman Yalçın City Hospital
        • コンタクト:

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
  • 高齢者

健康ボランティアの受け入れ

はい

サンプリング方法

非確率サンプル

調査対象母集団

Study participants will be selected from adults evaluated at the Physical Medicine and Rehabilitation outpatient clinic of Göztepe Prof. Dr. Süleyman Yalçın City Hospital. The patient group will include right-hand-dominant adults with unilateral shoulder pain lasting at least 3 months and a diagnosis of rotator cuff pathology. The control group will include right-hand-dominant healthy adults without shoulder pain who meet the study eligibility criteria.

説明

Inclusion Criteria:

Rotator Cuff Pathology Group

  • Willing to participate in the study and able to provide written informed consent
  • Aged 18 years or older
  • Unilateral shoulder pain lasting for at least 3 months
  • Right-hand dominance
  • Diagnosis of rotator cuff pathology

Healthy Control Group

  • Willing to participate in the study and able to provide written informed consent
  • Aged 18 years or older
  • Right-hand dominance
  • No current shoulder pain

Exclusion Criteria:

  • Unwilling or unable to provide written informed consent
  • Younger than 18 years
  • History of a chronic orthopedic or neurological condition that may affect shoulder, abdominal, or periscapular muscle function
  • History of injury or surgery involving the abdominal region
  • Bilateral shoulder pain or bilateral shoulder pathology
  • Chronic low back pain
  • Recent history of lumbar spine injury or surgery
  • Presence of a comorbid condition that may cause balance impairment
  • History of neuromuscular disease
  • History of malignancy
  • Pregnancy
  • Receipt of physical therapy or rehabilitation for the shoulder region within the previous 6 months

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

コホートと介入

グループ/コホート
Rotator Cuff Pathology Group
Adults with unilateral shoulder pain lasting at least 3 months and magnetic resonance imaging-confirmed rotator cuff pathology.
Healthy Control Group
Healthy adults without shoulder pain or a known history of rotator cuff pathology.

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
Abdominal Muscle Thicknesses
時間枠:During the single assessment visit at enrollment (Day 1)
The thicknesses of the rectus abdominis, external oblique, internal oblique, and transversus abdominis muscles will be measured separately in millimeters using diagnostic ultrasonography. Participants will be assessed in the supine position with a pillow placed under the knees. Lateral abdominal muscle measurements will be performed at the midpoint of a line drawn between the anterior superior iliac spine and the inferior border of the lowest rib at the midaxillary line. Rectus abdominis thickness will be measured immediately above the umbilicus at the thickest visible region of the muscle. Minimal transducer pressure will be applied to avoid compression of the muscle tissue. Each measurement will be repeated three times, and the mean of the three measurements will be used in the analysis.
During the single assessment visit at enrollment (Day 1)

二次結果の測定

結果測定
メジャーの説明
時間枠
Latissimus Dorsi Muscle Thickness
時間枠:During the single assessment visit at enrollment (Day 1)
Latissimus dorsi muscle thickness will be measured with participants in the prone position, with both upper extremities relaxed and positioned alongside the body and the trunk maintained in a neutral position. The measurement site will be identified at the level of the 10th rib along a line drawn between the midpoint of the axilla and a point located 2 cm medial to the posterior superior iliac spine. The ultrasound transducer will be positioned perpendicular to the 10th rib at this level, and latissimus dorsi muscle thickness will be measured at this site. Minimal transducer pressure will be applied to avoid compression of the muscle tissue. Each measurement will be repeated three times, and the mean of the three measurements will be used in the analysis.
During the single assessment visit at enrollment (Day 1)
Static Postural Stability
時間枠:During the single assessment visit at enrollment (Day 1)
Static postural stability will be assessed using a pedobarographic platform. Participants will stand on the platform under standardized testing conditions, and postural sway parameters recorded by the system will be used to evaluate static balance. Higher postural sway values indicate poorer static postural stability.
During the single assessment visit at enrollment (Day 1)
Trunk Proprioception
時間枠:During the single assessment visit at enrollment (Day 1)
Trunk proprioception will be assessed using a digital inclinometer and the active repositioning method. Participants will sit at the edge of a bed with the feet supported, hips and knees flexed to 90°, and the pelvis stabilized. The inclinometer will be positioned over the T4 spinous process. After three practice trials, participants will perform 30° trunk flexion with their eyes open and maintain the target position for 5 seconds. They will then return to the target position with their eyes closed. The absolute difference between the target and reproduced angles will be recorded in degrees. Three measurements will be performed, and the mean repositioning error will be used in the analysis. Higher values indicate poorer trunk proprioception.
During the single assessment visit at enrollment (Day 1)
Timed Up and Go Test (TUG)
時間枠:During the single assessment visit at enrollment (Day 1)
Functional mobility will be assessed using the Timed Up and Go Test. Participants will be instructed to rise from a chair, walk a distance of 3 meters at a comfortable pace, turn, walk back to the chair, and sit down. The time required to complete the test will be recorded in seconds. A longer completion time indicates poorer functional mobility.
During the single assessment visit at enrollment (Day 1)
Walking Speed
時間枠:During the single assessment visit at enrollment (Day 1)
Walking speed will be assessed during a standardized walking test and calculated in meters per second by dividing the walking distance by the time required to complete the test. A higher value indicates a faster walking speed.
During the single assessment visit at enrollment (Day 1)
Abdominal Flexion and Lateral Flexion Muscle Strength
時間枠:During the single assessment visit at enrollment (Day 1)
Abdominal flexion and lateral flexion muscle strength will be assessed using standardized manual muscle testing procedures. Muscle strength will be graded on an ordinal scale from 0 to 5, where 0 indicates no visible or palpable muscle contraction and 5 indicates the ability to complete the movement against full manual resistance.
During the single assessment visit at enrollment (Day 1)
Flexor Endurance Test
時間枠:During the single assessment visit at enrollment (Day 1)
Trunk flexor endurance will be assessed using the flexor endurance test. Participants will sit with the trunk supported at approximately 60°, the hips and knees flexed to 90°, and the arms crossed over the chest. The support will then be moved approximately 10 cm backward, and participants will be instructed to maintain the position for as long as possible. The test will end when the trunk falls below the 60° position. The duration will be recorded in seconds, with shorter times indicating lower trunk flexor endurance.
During the single assessment visit at enrollment (Day 1)

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。

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 (推定)

2026年8月1日

一次修了 (推定)

2026年10月1日

研究の完了 (推定)

2026年11月1日

試験登録日

最初に提出

2026年7月30日

QC基準を満たした最初の提出物

2026年7月30日

最初の投稿 (実際)

2026年8月4日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月4日

QC基準を満たした最後の更新が送信されました

2026年7月30日

最終確認日

2026年7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

Individual participant data will not be shared because participant consent was obtained for use of the data within the scope of this study, and no data-sharing plan was established in the study protocol.

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

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