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Clinical Trials/NCT03958227
NCT03958227
Completed
Not Applicable

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

Istanbul University1 site in 1 country30 target enrollmentMay 20, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Glenohumeral Arthritis
Sponsor
Istanbul University
Enrollment
30
Locations
1
Primary Endpoint
Shoulder Range of Motion (ROM)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

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.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
May 20, 2019
End Date
December 30, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sibel Gayretli Atan

Physiotherapist

Istanbul University

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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

Outcomes

Primary Outcomes

Shoulder Range of Motion (ROM)

Time Frame: 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.

Secondary Outcomes

  • 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.)

Study Sites (1)

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