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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03413488
Other study ID # 201705117RIND
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 16, 2018
Est. completion date December 18, 2018

Study information

Verified date February 2019
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the effect between the exercise intervention (strengthening exercise and stretching exercise) and exercise intervention with taping on decreasing round shoulder posture and improving symptoms in subjects with shoulder impingement syndrome/round shoulder syndrome.


Description:

Background: Poor posture and abnormal scapular kinematics have been suggested as possible primary factors in developing Shoulder impingement syndrome (SIS) and also as secondary observed phenomena of SIS. Round shoulder posture (RSP) is major and common posture contributing to increase the potential for subacromial impingement or exaggerate the symptoms of SIS. Objective: To compare the effect between the exercise intervention (strengthening exercise and stretching exercise) and exercise intervention with taping on decreasing RSP and improving symptoms in subjects with SIS/RSP. Methods: Forty subjects with impingement age between 20 and 75 are recruited and measured on acromial distance, pectoralis minor index (PMI), posterior and anterior shoulder tightness, distance of scapular medial border, pain score and flexilevel scale of shoulder function (FLEX-SF). Clinical significance: Shoulder impingement syndrome (SIS) have been identified as the majority of reported shoulder complaints. The project will provide an effective intervention for subjects with SIS/RSP.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 18, 2018
Est. primary completion date December 14, 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years to 75 Years
Eligibility Inclusion criteria:

1. subjects age between 20 and 75

2. Diagnosed with shoulder impingement syndrome

3. At least three positive of five tests, including Neer's test, Hawkin's test, Empty can test, tenderness in tendon of rotator cuff

Exclusion criteria:

1. Shoulder pain onset due to trauma

2. A history of shoulder fractures or dislocation

3. Cervical radiculopathy

4. Degenerative joint disease of the shoulder

5. Surgical interventions on the shoulder

6. Inflammatory arthropathy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
kinesio taping
Apply exercise and kinesio taping for intervention
exercise
Apply only exercise intervention

Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Length of the pectoralis minor The Pectoralis minor index (PMI) is calculated by dividing the resting muscle length by the subject's height and multiplying by 100. 1 year
Primary Acromial distance (AD) Acromial distance is defined as the distance from table to border of lateral-inferior acromion and measured in centimeter. 1 year
Primary Posterior and anterior shoulder tightness Flexibility of the posterior and anterior shoulder tissues, measured in degree 1 year
Primary Distance of scapular medial border The distance from the root of the spine (ROS) and the inferior angle (INF) of the scapula to the thoracic wall in millimeter respectively 1 year
Primary Self-reported flexilevel scale of shoulder function (FLEX-SF) FLEX-SF is used to assess shoulder function and disability. Scores will be recorded from 1, with the most limited function, to 50, without any limited function in the subject. 1 year
Primary Pain score Severity of pain is measured by Visual Analogue Scale, providing a range of scores from 0-10. 1 year