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临床试验/NCT07525297
NCT07525297尚未招募不适用

The Effect of Adding Thoracic Mobilization to Mulligan's Mobilization With Movement in Individuals With Rotator Cuff Pathology

Yuzuncu Yil University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年4月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
Range of motion

研究概览

简要总结

Rotator cuff pathology is defined as the degeneration or tear of one or more of the muscles or tendons of the rotator cuff, namely the supraspinatus, infraspinatus, teres minor, and subscapularis. Shoulder girdle biomechanics are not solely comprised of the glenohumeral joint but are built upon a kinetic chain involving the synchronized movement of the scapula, clavicle, and thoracic spine. In this context, the concept described in the literature as the "Regional Dependence" model argues that functional impairment in a distal segment like the shoulder may stem from or exacerbate limitations in a more proximal region like the thoracic spine. Conventional treatment approaches that focus solely on the shoulder joint may have limited clinical outcomes due to neglecting the fundamental link in the kinetic chain. Maintained natural apophyseal glides (SNAGs), a cornerstone of Mulligan's Concept in spinal rehabilitation, are a dynamic manual therapy technique aimed at correcting microscopic misalignments in facet joints during active movement. The aim of this randomized controlled trial is to investigate the effects of thoracic mobilization added to the Mulligan movement shoulder mobilization technique on pain intensity, range of motion, proprioception, and upper extremity functionality in individuals with rotator cuff pathology, and to evaluate the superiority of this combined approach over shoulder mobilization alone. Assessments will be performed before treatment and at the end of the 3-week intervention. Rest and activity pain intensity will be assessed using the Pain Numerical Rating Scale (PMR), shoulder range of motion using a digital goniometer, thoracic kyphosis degrees using a smartphone with the 'Angle Meter' software installed and calibrated gyroscope and accelerometer sensors, functionality using the Shoulder Pain and Disability Index (SPAI), and proprioception using a laser pointer and target device. The obtained data will be compared using appropriate statistical analysis methods. This study is expected to provide scientific evidence regarding the clinical effectiveness of thoracic mobilization technique added to shoulder mobilization technique applied in conjunction with conventional treatment in individuals with rotator cuff pathology, and to contribute to filling the methodological gap mentioned in the literature.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Having been diagnosed with unilateral rotator cuff pathology (impingement syndrome, tendinopathy, or partial tear) by a specialist physician through clinical examination and/or radiological imaging (USG/MR);
  • Being between 18 and 65 years of age;
  • Having shoulder pain that has persisted for at least 3 months;
  • Having a positive result on at least two of the Neer, Hawkins-Kennedy, and Empty Can tests;
  • Having a pain intensity of at least 3/10 on the Pain Numerical Rating Scale (NPRS) during rest or activity;
  • Having sufficient cognitive ability to follow simple instructions and administer the tests;
  • Having a Mini Mental State Test score ≥24;
  • Having the ability to provide signed informed consent and agreeing to participate in the study voluntarily.

排除标准

  • Having undergone previous surgery on the shoulder or thoracic region;
  • Having full-thickness rotator cuff tears requiring surgical indication;
  • Having adhesive capsulitis, shoulder instability, labrum tears, or calcific tendinitis;
  • Having cervical radiculopathy or neurological diseases affecting the upper extremity;
  • Having uncontrolled diabetes, inflammatory rheumatic diseases (rheumatoid arthritis, etc.), or malignancy;
  • Having severe osteoporosis, unstable vertebral fractures, or active infection in the thoracic region;
  • having received steroid (cortisone) or PRP injections to the shoulder region within the last 3 months.

研究组 & 干预措施

Control Group

Active Comparator

Conventional Physiotherapy Program, Mulligan Mobilization with Movement

干预措施: Mulligan Mobilization with Movement (Procedure)

Control Group

Active Comparator

Conventional Physiotherapy Program, Mulligan Mobilization with Movement

干预措施: Conventional Physiotherapy Program (Other)

Intervention Group

Experimental

Conventional Physiotherapy Program, Mulligan Mobilization with Movement and Thoracic Spine Mobilization

干预措施: Mulligan Mobilization with Movement (Procedure)

Intervention Group

Experimental

Conventional Physiotherapy Program, Mulligan Mobilization with Movement and Thoracic Spine Mobilization

干预措施: Thoracic Spine Mobilization (Procedure)

Intervention Group

Experimental

Conventional Physiotherapy Program, Mulligan Mobilization with Movement and Thoracic Spine Mobilization

干预措施: Conventional Physiotherapy Program (Other)

结局指标

主要结局

Range of motion

时间窗: "From enrollment to the end of treatment at 3 weeks

Range of motion will be assessed using a universal goniometer.

Thoracic kyphosis angle

时间窗: From enrollment to the end of treatment at 3 weeks

Participants' thoracic kyphosis degrees will be measured via a smartphone equipped with 'Angle Meter' software, a digital inclinometer.

Proprioception

时间窗: "From enrollment to the end of treatment at 3 weeks

Proprioception will be assessed using a laser pointer and millimeter graph paper. The laser pointer will be secured to the participant's arm just above the lateral epicondyle, parallel to the arm, using an elastic bandage. The participant will be positioned in a seated position 1 meter away from the millimeter graph paper. The amount of linear deviation on the millimeter graph paper will be converted into angular error using a trigonometric formula based on the distance between the center of the shoulder joint and the paper.

次要结局

  • Shoulder pain(From enrollment to the end of treatment at 3 weeks)
  • Shoulder Functionality(From enrollment to the end of treatment at 3 weeks)

研究者

发起方
Yuzuncu Yil University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ayse Merve TAT

Assistant Professor

Yuzuncu Yil University

研究点 (1)

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