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Trial record 4 of 28 for:    Recruiting, Not yet recruiting, Available Studies | "Shoulder Impingement Syndrome"

Effectiveness of Eccentric and Concentric Strength Training in Patients With Subacromial Impingement Syndrome

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ClinicalTrials.gov Identifier: NCT03186287
Recruitment Status : Recruiting
First Posted : June 14, 2017
Last Update Posted : July 23, 2019
Sponsor:
Information provided by (Responsible Party):
Damla Karabay, Izmir Katip Celebi University

Brief Summary:
The purpose of this study is to investigate and compare the effects of eccentric and concentric strength training on pain, strength, joint position sense and function in patients with subacromial impingement syndrome.

Condition or disease Intervention/treatment Phase
Subacromial Impingement Syndrome Other: Eccentric training Other: Concentric training Other: Standard physiotherapy Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 45 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: Effectiveness of Eccentric and Concentric Strength Training in Patients With Subacromial Impingement Syndrome: A Randomized Controlled Trial
Actual Study Start Date : September 21, 2017
Estimated Primary Completion Date : March 21, 2020
Estimated Study Completion Date : March 21, 2020

Arm Intervention/treatment
Experimental: Eccentric training group
The participants in this group will actively perform eccentric phase of resistive shoulder exercises. Additionally they will receive standard physiotherapy.
Other: Eccentric training
Eccentric phase of resistive shoulder exercises will be performed three sets of 15 repetitions once a day for 12 weeks using therabands. Participants will be supervised by the physiotherapist 3 days a week for the first 6 weeks, 2 days a week for the next 3 weeks and 1 day a week for the last 3 weeks.

Other: Standard physiotherapy
The participants will receive standard physiotherapy. The standard physiotherapy exercises will be supervised by the physiotherapist, same as intervention exercises.

Experimental: Concentric training group
The participants in this group will actively perform concentric phase of resistive shoulder exercises. Additionally they will receive standard physiotherapy.
Other: Concentric training
Concentric phase of resistive shoulder exercises will be performed three sets of 15 repetitions once a day for 12 weeks using therabands. Participants will be supervised by the physiotherapist 3 days a week for the first 6 weeks, 2 days a week for the next 3 weeks and 1 day a week for the last 3 weeks.

Other: Standard physiotherapy
The participants will receive standard physiotherapy. The standard physiotherapy exercises will be supervised by the physiotherapist, same as intervention exercises.

Active Comparator: Control group
The participants in this group will receive only standard physiotherapy.
Other: Standard physiotherapy
The participants will receive standard physiotherapy. The standard physiotherapy exercises will be supervised by the physiotherapist, same as intervention exercises.




Primary Outcome Measures :
  1. Shoulder Function [ Time Frame: Baseline, 12 weeks and 24 weeks ]
    Change of Constant Murley Score


Secondary Outcome Measures :
  1. Pain intensity [ Time Frame: Baseline, 12 weeks and 24 weeks ]
    Change of visual analog scale score in activity and rest

  2. Upper extremity function [ Time Frame: Baseline, 12 weeks and 24 weeks ]
    Change of disabilities of the arm, shoulder, and hand (DASH) score

  3. Isometric strength [ Time Frame: Baseline, 12 weeks and 24 weeks ]
    Change of shoulder abduction and external rotation isometric strength (in kg, with hand held dynamometer)

  4. Eccentric strength [ Time Frame: Baseline, 12 weeks and 24 weeks ]
    Change of shoulder abduction and external rotation eccentric strength (in kg, with hand held dynamometer)

  5. Joint position sense [ Time Frame: Baseline, 12 weeks and 24 weeks ]
    Change of shoulder joint repositioning angle errors (with bubble inclinometer)



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of subacromial impingement syndrome
  • Complaints associated with subacromial impingement syndrome for at least 3 months
  • No extra pain with 90 degree abduction-90 degree external rotation position of the shoulder
  • Ability to complete the entire study procedure

Exclusion Criteria:

  • Severe pain; shoulder pain is > 7/10
  • History of upper extremity fracture
  • History of shoulder, cervical and thoracic surgery
  • Having shoulder instability or frozen shoulder diagnosis
  • History of shoulder injuries, trauma and / or shoulder symptoms requiring treatment during the last 1 year (except than subacromial impingement syndrome)
  • Full-thickness rotator cuff tear
  • Systemic musculoskeletal disease
  • Neck and shoulder pain with cervical spine movement
  • Chest deformity or scoliosis diagnosis

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03186287


Contacts
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Contact: Damla KARABAY, MSc +902323293535 damla.gulpinar@ikc.edu.tr

Locations
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Turkey
Dokuz Eylul University, School of Physical Therapy and Rehabilitation Recruiting
İzmir, Balçova, Turkey, 35340
Contact: Damla KARABAY, MS    +902323293535    damla.gulpinar@ikc.edu.tr   
Sponsors and Collaborators
Dokuz Eylul University
Investigators
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Principal Investigator: Damla KARABAY, MSc Izmir Katip Celebi University
Study Director: Sevgi Sevi YESILYAPRAK, PhD Dokuz Eylul University
Study Director: Mehmet ERDURAN, MD Dokuz Eylul University
Study Director: Cem OZCAN, MD Izmır Katip Celebi University Atatürk Training and Research Hospital

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Responsible Party: Damla Karabay, MSc, Izmir Katip Celebi University
ClinicalTrials.gov Identifier: NCT03186287     History of Changes
Other Study ID Numbers: 2837-GOA
First Posted: June 14, 2017    Key Record Dates
Last Update Posted: July 23, 2019
Last Verified: July 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Shoulder Impingement Syndrome
Syndrome
Rotator Cuff Injuries
Disease
Pathologic Processes
Rupture
Wounds and Injuries
Shoulder Injuries
Tendon Injuries
Joint Diseases
Musculoskeletal Diseases