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临床试验/NCT03958227
NCT03958227已完成不适用

Istanbul University, Faculty of Health Science, Division of Physiotherapy and Rehabilitation

Istanbul University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2019年5月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30
试验地点
2
主要终点
Shoulder Range of Motion (ROM)

研究概览

简要总结

The aim of the investigator's study is to compare the efficacy of manual therapy and exercise practices compared to exercise practice in patients with Glenohumeral Arthritis. Thirty volunteer patients will include into the study.

详细描述

Patients will randomly divide into two groups. A common exercise program was applied to both groups during 15 sessions. Manual therapy techniques will apply to the manual therapy group in addition to exercise practices. Patients will evaluate in terms of functional status, pain, range of motion, muscle strength and health-related quality before and after 5 weeks of treatment. Also, patient's satisfaction from treatment will evaluate at the 5th week of the treatment. DASH and ASES forms for functional status, VAS for pain, digital goniometer for range of motion, manual muscle test for muscle strength, SF-12 for health-related quality of life, and Global Rating of Change (GRC) Scale for patient satisfaction will be used as evaluation criteria.

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
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • 40 years and older patients
  • To be diagnosed with GHOA by specialist physician via MRI, US or radiography and physical examination
  • Unilateral shoulder pain lasting more than 2 months seen during daily living activities and at rest

排除标准

  • Patients with:
  • Severe arthrosis
  • Cervical radiculopathy
  • Emotional or cognitive problems
  • A neurological disease that causes muscle weakness on the shoulder
  • A skin disease that may affect upper extremity assessment.
  • Frozen shoulder
  • Thoracic outlet syndrome

结局指标

主要结局

Shoulder Range of Motion (ROM)

时间窗: Evaluation will be performed first time at baseline and second time will be performed after 5 weeks rehabilitation program. After treatment "change" will be assessed.

The shoulder flexion, abduction, internal and external rotation ROM will be evaluated with digital goniometer while the patient will be in supine position.

次要结局

  • Manual Muscle Test(Evaluation will be performed before treatment and after 5 weeks rehabilitation program.)
  • Short Form 12 (SF-12)(Evaluation will be performed before treatment and after 5 weeks rehabilitation program.)
  • Visual Analogue Scale (VAS)(Evaluation will be performed before treatment and after 5 weeks rehabilitation program.)
  • Global Rating of Change (GRC) Scale(Evaluation will be performed after 5 weeks rehabilitation program.)
  • ASES (The American Shoulder and Elbow Surgeons Standardized Shoulder Assessment) Form(Evaluation will be performed before treatment and after 5 weeks rehabilitation program.)
  • The Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire(Evaluation will be performed before treatment and after 5 weeks rehabilitation program.)

研究者

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

Sibel Gayretli Atan

Physiotherapist

Istanbul University

研究点 (2)

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