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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03246698
Other study ID # 3413-GOA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 28, 2017
Est. completion date July 20, 2019

Study information

Verified date July 2022
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 effect of isolytic and static stretching training in individuals having subacromial impingement syndrome with glenohumeral internal rotation deficit. Isolytic group will receive isolytic stretching in modified cross body stretching position and standard physiotherapy program. Static group will receive static stretching in modified cross body stretching position and standard physiotherapy program. Control group will receive only standard physiotherapy program.


Description:

The effectiveness of static stretching on various parameters such as range of motion or pain is studied and proved in literature. Static stretching in cross body position was also found helpful for improving shoulder range of motion with some disadvantages. In modified cross body position, the patient is positioned in a more advantageous way for him/her. Usually this stretching is done as active-assistive static stretching with the physiotherapist. Proof is still needed for the effectiveness of active-assistive static stretching in modified cross body position. Furthermore, there is no research about the effect of isolytic stretching which is relatively new technique compare to static stretches in subacromial impingement syndrome. In isolytic stretching, when the patient contracts the agonist muscle group with 20% muscle force active-assistive streching in agonist muscle group by the physiotherapist at the same time is done for 2-4 seconds. A fast isolytic stretching is applied in order to break the fibrous tissue. Our purpose is to investigate and compare the effect of isolytic and static stretching training in individuals having subacromial impingement syndrome with glenohumeral internal rotation deficit . Stretching groups will receive either isolytic or static stretching in modified cross body stretching position and standard physiotherapy program. There is a control group. Control group will receive only standard physiotherapy program. Standard physiotherapy program includes TENS, hotpack, posture and strengthening training program. Treatment program will last four times a week (4-4-4-3) for four weeks, 15 sessions in total.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date July 20, 2019
Est. primary completion date June 20, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis of subacromial impingement syndrome - Glenohumeral internal rotation range of motion of the affected shoulder should be less than other shoulder and bilateral shoulder internal rotation range of motion difference should be =15 º - Pain with resisted arm elevation or external rotation as well as a minimum of 3 of 5 positive subacromial impingement syndrome tests, painful arc, pain or weakness with resisted external rotation, Neer, Hawkins and Jobe tests. - Ability to complete the entire study procedure Exclusion Criteria: - A 50% limitation of passive shoulder range of motion in >2 planes of motion - Pain >7/10 - A history of fracture to the shoulder girdle - Systemic musculoskeletal disease - History of shoulder and cervical surgery - Glenohumeral instability (positive apprehension, relocation, or positive sulcus test) or positive findings for a full-thickness rotator cuff tear (positive lag sign, positive drop arm test, or marked weakness with shoulder external rotation) - Neck and shoulder pain with active/passive cervical spine movement - A diagnosis of chest deformity or scoliosis - Regularly performing posterior shoulder stretching exercises

Study Design


Intervention

Other:
Isolytic Stretching group
In modified cross body position, isolytic stretching exercises will perform five times each for 15 seconds. After each stretching patient will rest for 5 seconds. When the patient contracts the agonist muscle group with 20% muscle force, the agonist muscle group is stretched at the same time for 2-4 seconds. Isolytic stretching exercises will perform four times a week for four weeks. It's obligatory to receive at least 15 sessions in total. They will also receive standard physiotherapy program four times a week for four week, 15 sessions in total.
Static Stretching group
In modified cross body position, active-assistive static stretching exercises will be performed 5 times each for 15 seconds. This stretching exercise is performed 5 times with 5 seconds intervals. Static stretching exercises will perform four times a week for four weeks. It's obligatory to receive at least 15 sessions in total. They will also receive standard physiotherapy program four times a week for four week, 15 sessions in total.
Control group
They will receive only standard physiotherapy program, four times a week for four weeks, 15 sessions in total.

Locations

Country Name City State
Turkey Dokuz Eylül University 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 internal rotation range of motion Change of shoulder internal rotation range of motion (with bubble inclinometer) Baseline and 4 weeks
Secondary Glenohumeral internal rotation deficit Change of difference in shoulder internal rotation range of motion between the affected and non-affected shoulder (with bubble inclinometer) Baseline and 4 weeks
Secondary Posterior shoulder tightness Change of posterior shoulder tightness (with bubble inclinometer) Baseline and 4 weeks
Secondary Shoulder external rotation range of motion Change of shoulder external rotation range of motion (with bubble inclinometer) Baseline and 4 weeks
Secondary Shoulder total rotational range of motion Change of shoulder total rotational range of motion (Sum of the internal and external rotation motion) Baseline and 4 weeks
Secondary Resting and activitiy pain in shoulder Change of visual analog scale score in activity and rest pain Baseline and 4 weeks
Secondary Subacromial space Change of subacromial space at arm resting at the side (0°), and at 60° of scapular plane elevation (with Ultrasound) Baseline and 4 weeks
Secondary Supraspinatus tendon thickness Change of supraspinatus tendon thickness (with Ultrasound) Baseline and 4 weeks
Secondary Concentric strength Change of rotattor cuff muscles concentric strength (in kg, with hand held dynamometer) Baseline and 4 weeks
Secondary Eccentric strength Change of shoulder abduction eccentric strength (in kg, with hand held dynamometer) Baseline and 4 weeks
Secondary Shoulder Function Change of Modified Constant-Murley Score Baseline and 4 weeks
Secondary Upper extremity function Change of disabilities of the arm, shoulder, and hand (Quick-DASH) score Baseline and 4 weeks
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