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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04552925
Other study ID # 2016/1507
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 22, 2020
Est. completion date December 30, 2021

Study information

Verified date February 2022
Source Istanbul University-Cerrahpasa
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There are very few studies in the literature about conservative treatment of massive rotator cuff (RC) tears. Whether the treatment of massive RC tears is conservative or surgical is decided according to the age, activity level, expectation and additional pathologies of the patient. The aim of conservative treatment is to make the patient functionally independent and to reduce pain. In recent years, there are different opinions in the literature about the effectiveness of conservative treatment of massive RC tears. However, in recent biomechanical studies, it has been reported that the RC and the deltoid, which remain intact in massive RC tears, can function well together. The hypothesis of this study is that the deltoid-focused physiotherapy program, where strengthening exercises are performed with EMG biofeedback, will give more positive results in terms of range of motion (ROM), functional status, muscle strength, pain and patients satisfaction. aim of our study is to investigate the efficacy of electromyographic biofeedback (EMG-BF) device which was added to deltoid focused conservative treatment program in massive RC tears.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date December 30, 2021
Est. primary completion date December 29, 2020
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - Unilateral, non-traumatic massive rotator cuff tears according to Deorio and Cofield classification - Age older than 50 years and attend 1-year follow-up assessment Exclusion Criteria: - Patients with symptomatic lesions in the contralateral shoulder - Cuff tear arthropathy - Glenohumeral osteoarthritis - Pseudoparalytic shoulder - Grade 3-4 fatty degeneration according to Goutallier classification - History of involved shoulder surgery - Major systemic conditions that disallowing exercise

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Rehabilitation
Exercises and rehabilitation for massive rotator cuff tears

Locations

Country Name City State
Turkey Istanbul University Cerrahpasa Istanbul

Sponsors (2)

Lead Sponsor Collaborator
Istanbul University-Cerrahpasa Istanbul University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary American shoulder and elbow (ASES) score The American Shoulder and Elbow Surgeons Standardized Shoulder Assessment Form (ASES) is a standard shoulder assessment form, which is comprised of objective and subjective sections and prepared by shoulder and elbow surgeons. 12 months
Primary Deltoid Strength Measurement of the strength of the deltoid muscle with a digital dynamometer. 12 months
Secondary Range of Motion (ROM) Active ROM will evaluate with a universal goniometer. 12 months
Secondary Numeric Pain Rating Scale (NPRS) Participants' level of pain will assess by numeric pain rating scale (NPRS). 12 months
Secondary Global rating of change scale (GRCS) The global rating of change scale (GRCS) which is five-point Likert scale will be use to evaluate the difference between the participants' health status from their perspective. It is ranging from -2 (very much worse), through 0 (unchanged) to +2 (much better). 12 months
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