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临床试验/NCT07369934
NCT07369934招募中不适用

Virtual Reality Based Exercise Training Versus Mulligan Mobilization on Shoulder Posture and Function in Subacromial Impingement Syndrome

Cairo University1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2025年12月13日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
74
试验地点
1
主要终点
Pain intensity during shoulder elevation

研究概览

简要总结

The study will compare the effect of virtual reality based exercise training versus Mulligan mobilization in addition to exercise therapy added to both groups on shoulder posture and function in subacromial impingement syndrome.

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
Single (Participant)

入排标准

年龄范围
30 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Patients will be referred from the orthopedic surgeon with a diagnosis of stage II SIS with the following criteria:
  • Participants ranged in age from 30-50 years old.
  • Participants are from non-athletes from the general population.
  • Unilateral shoulder pain that is localized either anteriorly or laterally to the acromion. Pain that occurs or worsens when the affected shoulder is in flexion and/or abduction.
  • Four of the following should be present in the included patients: Neer impingement test, Hawkins' test, Pain was replicated in the supraspinatus empty-can test, a painful arc of movement from 70° to 120°, and painful greater tuberosity of the humerus.
  • BMI range 18.5- 29.9 Kg/m².

排除标准

  • 1) Patients who, during the previous three months, underwent shoulder physical treatment and/or an acute pain flare.
  • 2) Patients who have undergone surgeries for tendon repair. 3) Malignancy, epilepsy, pregnant women, and/or systemic conditions like chronic renal or liver failure.
  • 4) Mini-Mental State Examination test (MMSE) (< 24/30) to exclude cognitive impairment and/or significant vision impairment (if they couldn't read the introduction while wearing the Head Mounted Device (HMD).
  • 5) Corticosteroid injection during the last three months or used steroids chronically.
  • 6) Adhesive capsulitis, glenohumeral joint instability, Numbness or tingling of the upper limb, and/or full-thickness tear of the rotator cuff.

研究组 & 干预措施

Virtual reality group

Active Comparator

干预措施: Virtual Reality (Other)

Mulligan mobilization group

Active Comparator

干预措施: Mulligan mobilization (Other)

结局指标

主要结局

Pain intensity during shoulder elevation

时间窗: pain intensity at the start of session 1 to the end of 1 month of treatment

It will be measured using the Numerical Pain Rating Scale (NPRS)

Shoulder function

时间窗: shoulder function at the start of session 1 to the end of 1 month of treatment

The Shoulder Pain and Disability Index (SPADI) will be used to measure the shoulder function.

Shoulder flexion range of motion

时间窗: shoulder flexion at the start of session 1 to the end of 1 month of treatment

The Clinometer Application will be used to measure it.

Shoulder abduction range of motion

时间窗: shoulder abduction at the start of session 1 to the end of 1 month of treatment

The Clinometer Application will be used to measure it.

shoulder posture

时间窗: shoulder posture at the start of session 1 to the end of 1 month of treatment

Sagittal Shoulder Angle will be used to measure the shoulder posture

次要结局

  • Patients' enjoyment(It will be evaluated at the end of the last session (after 1 month))
  • patients' adherence to treatment sessions(patients' adherence at the start of session 1 to the end of 1 month of treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sara Mohsen Sayed Meselhy

Demonstrator at the Faculty of Physical Therapy, Cairo University

Cairo University

研究点 (1)

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