The Physiotherapy Approaches in Patients With Subacromial Impingement Syndrome

Sponsor
Istanbul University - Cerrahpasa (IUC) (Other)
Overall Status
Completed
CT.gov ID
NCT06156475
Collaborator
(none)
48
1
2
7
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Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Proprioception exercises
  • Procedure: Proprioception exercises with Electromyographic Biofeedback
  • Procedure: Wand Exercise
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
48 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The study consisted of patients with subacromial impingement syndrome evaluated by an orthopedist. Patients who met the inclusion criteria were divided into two groups.The study consisted of patients with subacromial impingement syndrome evaluated by an orthopedist. Patients who met the inclusion criteria were divided into two groups.
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
The Effect of Electromyographic Biofeedback and Proprioception Exercises on Pain and Functionality in Patients With Subacromial Impingement Syndrome: A Randomized Controlled Study
Actual Study Start Date :
May 1, 2021
Actual Primary Completion Date :
Aug 1, 2021
Actual Study Completion Date :
Dec 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Proprioception Exercise Group

Wand exercises and Proprioception exercises

Procedure: Proprioception exercises
Patients trained for proprioception exercises.

Procedure: Wand Exercise
Patients were educated with wand exercises.

Active Comparator: Proprioception exercises with Electromyographic Biofeedback

Wand exercises and Proprioception exercises with Electromyographic Biofeedback

Procedure: Proprioception exercises with Electromyographic Biofeedback
Patients trained for Proprioception exercises with Electromyographic Biofeedback

Procedure: Wand Exercise
Patients were educated with wand exercises.

Outcome Measures

Primary Outcome Measures

  1. Disabilities of the Arm, Shoulder and Hand scale [8 weeks]

    The Disabilities of the Arm, Shoulder and Hand scale was used to measure shoulder function.

Secondary Outcome Measures

  1. Visual analogue scale [8 weeks]

    The severity of pain was measured Visual analogue scale.

  2. Joint range of motion [8 weeks]

    Active shoulder flexion, abduction, and external-internal rotation range of motion was measured with goniometer.

  3. Muscle strength [8 weeks]

    Shoulder flexion, abduction, and external-internal rotator muscle strength was measured with manual muscle tester.

  4. Proprioception [8 weeks]

    To evaluate joint position sense, laser pointer-assisted angle reproduction test was applied for measurements at 55°-90°-125° flexion and abduction angles.

  5. Patient satisfaction [8 weeks]

    The amount of improvement or deterioration in patients was assessed with the Global Rating Change Scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istanbul Aydin University Istanbul Florya Turkey

Sponsors and Collaborators

  • Istanbul University - Cerrahpasa (IUC)

Investigators

  • Principal Investigator: Ebru Kaya Mutlu, Professor, Bandırma Onyedi Eylül University
  • Study Chair: Buse Aydin, M.Sc., Istabul Aydin University
  • Study Chair: Yasemin Karaaslan, Asst. Prof., Mustafa Kemal University
  • Study Chair: Hanifegül Taskiran, Professor, Istanbul Aydın University
  • Study Chair: Nezih Ziroglu, MD, Acıbadem Mehmet Ali Aydınlar University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ebru Kaya Mutlu, PT, Prof. Dr., Istanbul University - Cerrahpasa (IUC)
ClinicalTrials.gov Identifier:
NCT06156475
Other Study ID Numbers:
  • Istanbul Aydin University
First Posted:
Dec 5, 2023
Last Update Posted:
Dec 5, 2023
Last Verified:
Nov 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ebru Kaya Mutlu, PT, Prof. Dr., Istanbul University - Cerrahpasa (IUC)
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 5, 2023