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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03186287
Other study ID # 2837-GOA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 21, 2017
Est. completion date March 16, 2020

Study information

Verified date April 2020
Source Dokuz Eylul University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date March 16, 2020
Est. primary completion date March 16, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

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

Locations

Country Name City State
Turkey Dokuz Eylul University, School of Physical Therapy and Rehabilitation Izmir Balçova

Sponsors (1)

Lead Sponsor Collaborator
Dokuz Eylul University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shoulder Function Change of Constant Murley Score Baseline, 12 weeks and 24 weeks
Secondary Pain intensity Change of visual analog scale score in activity and rest Baseline, 12 weeks and 24 weeks
Secondary Upper extremity function Change of disabilities of the arm, shoulder, and hand (DASH) score Baseline, 12 weeks and 24 weeks
Secondary Isometric strength Change of shoulder abduction and external rotation isometric strength (in kg, with hand held dynamometer) Baseline, 12 weeks and 24 weeks
Secondary Eccentric strength Change of shoulder abduction and external rotation eccentric strength (in kg, with hand held dynamometer) Baseline, 12 weeks and 24 weeks
Secondary Joint position sense Change of shoulder joint repositioning angle errors (with bubble inclinometer) Baseline, 12 weeks and 24 weeks
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