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The Physiotherapy Approaches in Patients With Subacromial Impingement Syndrome

NCT ID: NCT06156475

Last Updated: 2023-12-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-01

Study Completion Date

2021-12-01

Brief Summary

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The aim of this study is to investigate the effectiveness of Electromyographic Biofeedback with proprioception exercises on pain, range of motion, muscle strength, proprioception and functionality in patients with subacromial impingement syndrome.

Detailed Description

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This study is planned as a prospective, randomized clinical study. Patients with subacromial impingement syndrome who volunteered to participate in the study, met the inclusion criteria, and signed the consent form were randomly assigned to the proprioception exercise group and the proprioception exercise with electromyographic biofeedback group. Demographic and clinical data of the patients were recorded. Shoulder function with Disabilities of the Arm, Shoulder and Hand scale, pain with VAS, painless active shoulder flexion, abduction, and external-internal rotation with goniometer, muscle strength with Manual Muscle Tester, proprioception (55°-90°- 125° angles of flexion and abduction, and angular deviations) with the Laser-pointer assisted angle reproduction test were evaluated, and patient satisfaction was evaluated with The Global Rating of Change Scale. After the initial evaluations were completed, only proprioception exercises and proprioception exercises with EMG-BF were applied 2 days a week for 8 weeks. Additionally, both groups were given Want exercises.

Conditions

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Subacromial Impingement Syndrome

Keywords

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Shoulder impingement syndrome shoulder pain proprioception biofeedback

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The study consisted of patients with subacromial impingement syndrome evaluated by an orthopedist. Patients who met the inclusion criteria were divided into two groups.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Proprioception Exercise Group

Wand exercises and Proprioception exercises

Group Type EXPERIMENTAL

Proprioception exercises

Intervention Type PROCEDURE

Patients trained for proprioception exercises.

Wand Exercise

Intervention Type PROCEDURE

Patients were educated with wand exercises.

Proprioception exercises with Electromyographic Biofeedback

Wand exercises and Proprioception exercises with Electromyographic Biofeedback

Group Type ACTIVE_COMPARATOR

Proprioception exercises with Electromyographic Biofeedback

Intervention Type PROCEDURE

Patients trained for Proprioception exercises with Electromyographic Biofeedback

Wand Exercise

Intervention Type PROCEDURE

Patients were educated with wand exercises.

Interventions

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Proprioception exercises

Patients trained for proprioception exercises.

Intervention Type PROCEDURE

Proprioception exercises with Electromyographic Biofeedback

Patients trained for Proprioception exercises with Electromyographic Biofeedback

Intervention Type PROCEDURE

Wand Exercise

Patients were educated with wand exercises.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Being diagnosed with subacromial impingement syndrome,
* Being between the ages of 18 and 65,
* Not having received medical treatment,
* Not having received a shoulder-related physiotherapy program in the last year,
* Not having had any shoulder-related surgery,

Exclusion Criteria

* Neurological deficits of the upper extremity and the presence of another orthopedic disorder, rheumatic or congenital disease other than subacromial impingement syndrome,
* Presence of mental problem,
* Having received corticosteroid treatment in the last year,
* Upper extremity fracture,
* Acute cervical pathology,
* Having cardiovascular and systemic diseases that prevent working,
* Pregnancy,
* Those with communication problems.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role lead

Responsible Party

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Ebru Kaya Mutlu, PT

Prof. Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ebru Kaya Mutlu, Professor

Role: PRINCIPAL_INVESTIGATOR

Bandırma Onyedi Eylül University

Buse Aydin, M.Sc.

Role: STUDY_CHAIR

Istabul Aydin University

Yasemin Karaaslan, Asst. Prof.

Role: STUDY_CHAIR

Mustafa Kemal University

Hanifegül Taskiran, Professor

Role: STUDY_CHAIR

Istanbul Aydın University

Nezih Ziroglu, MD

Role: STUDY_CHAIR

Acıbadem Mehmet Ali Aydınlar University

Locations

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Istanbul Aydin University

Istanbul, Florya, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Istanbul Aydin University

Identifier Type: -

Identifier Source: org_study_id