Design: Randomized clinical trial.
Location: This study conducted at El Sahel teaching hospital, Egypt.
Subjects: Seventy five patients with shoulder impingement syndrome assigned into three equal groups. Their ages were ranged from 20- 40 years.
Intervention: The three groups received the same exercise program and group (A) received kinesiotaping over supraspinatus muscle and deltoid muscle, tape removed every 3 days and patients return back for retaping. Group (B) received laser with 4J / cm² for 90 sec over the greater tuberosity of humerus and deltoid insertion. Group (C) received exercises only. Treatment sessions were applied 3 times / week for 4 weeks for the three groups.
Outcome measures: Visual analogue scale was used to assess pain severity, shoulder pain and disability index was used to assess functional ability level and electrogoniometer was used to assess shoulder flexion and abduction range of motion.
Results: Pain level was markedly decreased in the kinesiotaping group than low level laser group or control group. Also shoulder functional level and shoulder flexion and abduction range of motion were improved in kinesiotaping group than the other groups.
Conclusion: According to the results of this study adding kinesiotaping or low level laser to exercise program is effective in treatment of shoulder impingement syndrome. While kinesiotaping is more effective than low level laser and produce better improvement in pain level, functional activity and shoulder range of motion.
Keywords: Kinesiotaping; Low level laser; Shoulder impingement
The recommended management of shoulder symptoms starts with educational information about the natural course of shoulder pain combined with the advise to avoid irritating and loading activities. The use of analgesics or NSAIDs is recommended for the first two weeks. When no recovery occurs within two weeks, sub acromial or intraarticular injection therapy with corticosteroids are administered and eventually repeated. Finally, physical therapy is only recommended after a 6-week period when there are functional limitations (specifically an activating and time-contingent approach) [4].
Many treatments for Shoulder Impingement Syndrome (SIS) are available in clinical practice; some of which have already been compared with other treatments by various investigators. However, a comprehensive treatment comparison is lacking. The evidence suggests that supervised and home-based progressive shoulder strengthening and stretching are effective for the management of sub acromial impingement syndrome [5].
Recently, kinesiotaping has become increasingly popular for a range of musculoskeletal conditions and for sport injuries [6].
Kinesiotaping is a technique which uses the application of an elastic adhesive tape on the skin. Kinesiotaping is manufactured with elastic cotton which can be stretched from 120 to 140% its original length. It is claimed that Kinesiotaping supports injured muscles and joints and helps to relieve pain by lifting the skin, thus improving blood and lymph flow [7].
Kinesiotaping is seemed to have effect in treatment of shoulder impingement as it might serves as an alternative treatment in case injection of corticosteroids are contraindicated [8].
Laser is a noninvasive, nonionizing, monochromatic electromagnetic high concentrated light beam. Recently, Low Level Laser Therapy (LLLT) is widely used in various rheumatologic and musculoskeletal disorders which have analgesic, anti‐inflammatory and bio stimulating effects. The LLLT induces cell proliferation, collagen synthesis, protein synthesis, tissue reparation, wound healing and pain relief through direct irradiation without thermal response [9].
LLLT may be considered as an effective alternative to ultrasound based therapy in patients with sub acromial impingement syndrome especially ultrasound based therapy is contraindicated [10].
As shoulder impingement syndrome is a common problem; selection of effective modalities for treatment is very important that give rise to the question whether adding kinesiotaping or LLLT to exercise program will produce better results or not.
Participant: The current study was conducted at El Sahel teaching hospital at Cairo, patient were referred from the outpatient orthopedic clinic at El Sahel teaching hospital after being examined by the orthopedist ,who was blinded about the treatment groups, to exclude patient with exclusion criteria (a copy of exclusion criteria were sent to orthopedic clinic). Based on power analysis, the sample size was 120 patients but not all the patient completes the study. Their ages were ranged from 25 to 40 years old. Subjects who participated in this study had at least 3 of the following inclusion criteria:
1.Positive Neer sign: The humerus was passively flexed to endrange with overpressure. Reproduction of pain confirms the presence of impingement syndrome.
2.Positive Hawkins sign: The shoulder was passively placed in approximately 90 degrees of flexion and is passively internally rotated to end-range with overpressure, reproducing patient’s pain.
3.Pain with active shoulder elevation in the scapular plane.
4.Pain with palpation of the rotator cuff tendons.
5.Pain with resisted isometric shoulder abduction.
Subjects had been excluded when they had any of the following exclusion criteria
1.Current symptoms related to cervical spine.
2.Positive tests for shoulder instability:
a.Sulcus sign: A positive sulcus sign was an excessive downward movement of the humeral head away from the acromion when an inferior pull is placed on the humerus while the arm was in a dependent position.
b.History of shoulder dislocation.
3.Acromioclavicular pain: with the arm flexed to approximately 90 degrees, pain was reproduced by passively adducting and internally rotating the humerus across the chest to approximate the acromioclavicular joint.
4. Frozen shoulder as a complication of rotator cuff impingement syndrome.
5.Any other pathology of shoulder as degenerative arthritis.
6.A history of pain in the C5- C6 dermatome.
After selection through consultation with an orthopedist, the patients provided their written consent and were given an opportunity to ask any questions regarding the procedure. The study program had been approved by the ethical committee of general organization of teaching hospitals and institutes. Sealed envelope used for allocation of patient over the 3 groups by other clinician who was blinded about the study, then pre-treatment measurement were applied by the main researcher who was blinded about to which group patient was allocated.
Patients were divided into three equal groups (A,B, and C). Group A: (n=25) received kinesiotaping with exercise program, group B: (n=25) received LLLT with exercise program and group C: (n=25) received exercise program only.
Treatment had been carried out in physical therapy outpatient clinic of El- Sahel teaching hospital. The program of the study was given for three groups three sessions per week for four weeks. All groups had received the same exercises (which includes flexibility and strengthening program. The flexibility program was consisting of stretching exercise for the posterior and inferior shoulder capsule. The strengthening exercise was performed for shoulder flexors and abductors by carrying a proper weights and elastic bands.
Group A: patients received the exercise program plus kinesiotaping over supraspinatus muscle and deltoid muscle, tape was removed every three days and subjects returned back to the clinic to reapplication of tape again. Patients receive the same therapeutic exercise as the other 2 groups 3 times/ week.
Group B: patients received the exercise program plus laser with 4J / cm² for 90 sec over the common trigger points in impingement syndrome which were: over the greater tuberosity of humerus and deltoid insertion 3 times/ week
Pain was assessed by using the visual analog scale, each subject was made aware the VAS as being 10 cm horizontal line with one end described as (no pain =0), and other end (the worst pain I ever felt = 10). Patients were asked to mark a point on the line between the extremes that relates to their level of pain.
The shoulder pain and disability index is an acceptable tool to measure disability caused by shoulder impingement syndrome in the general population. Patients were instructed to mark at the point which refers to their degree of pain during ADL in the first subscale, and to their degree of difficulty in performing ADL in the other subscale.
Each item is scored by measuring their distance from the left anchor to the mark made by the patient. Subscales are scored in a 3 part process. First, item scores within subscale are summed. Second, the sum is divided by the summed distance possible across all items of the subscale to which the person respond. Third, this ratio is multiplied by 100 to obtain a percentage. To obtain the SPADI total score, the pain and disability subscales scores are averaged [11].
Active shoulder flexion and abduction were measured by the electrogoniometer device. Every measurement was performed 3 times and the average measurement was recorded
For measuring flexion: The fulcrum of the electrogoniometer was fixed over the lateral border of the tip of acromion and the fixed arm stabilized parallel to lateral border of trunk, while the moveable arm stabilized on the lateral border of the humerus. The patient was instructed to move into full flexion as much as he can and at the end of movement the angle was recorded by the therapist.
For measuring abduction: The fulcrum of the electrogoniometer was fixed over the anterior border of the acromion process and the fixed arm stabilized parallel to the anterior border of trunk, while the moveable arm stabilized parallel to the anterior border of the humerus. The patient was instructed to move into full abduction as much as he can, and at the end of movement the angle was recorded by the therapist.
Statistical Values |
Age (Years) |
Weight (kg) |
Height (cm) |
Mean |
32.6 |
63.5 |
163.5 |
Standard error |
± 2.79 |
8.03 |
4.71 |
Pain level |
SS |
MS |
F |
P value |
S |
|
Pre Treatment |
Between Groups |
0.26 |
0.13 |
0.19 |
0 .82 |
NS |
Post Treatment |
Between Groups |
20.06 |
10.03 |
9.88 |
0 .001 |
S |
Functional disability level SPADI |
SS |
MS |
F |
P value |
S |
|
Pre Treatment |
Between Groups |
218.17 |
109.08 |
2.72 |
0 .08 |
NS |
Post Treatment |
Between Groups |
3542.2 |
1771.1 |
38.05 |
0 .0001 |
S |
Shoulder flexion |
SS |
MS |
F |
P value |
S |
|
Pre Treatment |
Between Groups |
220.86 |
110.43 |
0.91 |
0 .41 |
NS |
Post Treatment |
Between Groups |
2890.86 |
1445.43 |
10.07 |
0 .001 |
S |
Shoulder abduction |
SS |
MS |
F |
P value |
S |
|
Pre Treatment |
Between Groups |
154.46 |
77.23 |
0.68 |
0 .51 |
NS |
Post Treatment |
Between Groups |
3678.86 |
1839.43 |
16.23 |
0 .0001 |
S |
Pain level |
Mean difference |
P value |
S |
|
Post Treatment |
Group A vs group B |
1.1 |
0.02 |
S |
Group A vs. group C |
2.0 |
0.0001 |
S |
|
Group B vs. group C |
0.9 |
0.056 |
NS |
Shoulder flexion |
Mean difference |
P value |
S |
|
Post Treatment |
Group A vs. group B |
17.8 |
0.003 |
S |
Group A vs. group C |
22.9 |
0.0001 |
S |
|
Group B vs. group C |
5.1 |
0.35 |
NS |
For shoulder abduction ROM there was a significant difference in level of improvement between groups A and B, and there was a significant difference in level of improvement between groups A and C. While there was no significant difference in level of improvement between groups B and C as shown in [Table 9].
Functional disability level |
Mean difference |
P value |
S |
|
Post Treatment |
Group A vs. group B |
13.06 |
0.0001 |
S |
Group A vs. group C |
26.61 |
0.00001 |
S |
|
Group B vs. group C |
13.55 |
0.0001 |
S |
Shoulder abduction |
Mean difference |
P value |
S |
|
Post Treatment |
Group A vs. group B |
17.9 |
0.001 |
S |
Group A vs. group C |
26.6 |
0.0001 |
S |
|
Group B vs. group C |
8.7 |
0.07 |
NS |
It was concluded that strengthening of the rotator cuff muscles and scapular stabilizing muscles and stretching the soft tissues of the anterior and posterior shoulder were the options most supported physical therapy program [14]. In this study exercise program this exercise program was used in adjunction with two modalities (kinesiotaping and low level laser) that commonly used to treat pain to gain better results of physical therapy program.
In this study pain level was markedly decreased in the kinesiotaping group than low level laser group or control group. Also shoulder functional level and shoulder flexion and abduction range of motion were improved in kinesiotaping group than the other groups.
There are many studies support the use of kinesiotaping in different musculoskeletal problems and support its use as a prophylactic technique especially in sports medicine. It was suggested that kinesiotaping causes positive changes in scapular motion. This could support its use in sports medicine for preventing shoulder problems [15].
The effect of Kinesiotaping in shoulder impingement may be due to its effect on acomiohumeral distance as it was found that kinesiotaping increases acromiohumeral distance in healthy individuals immediately following application, compared with sham kinesiotape [16]. Also it has positive effect on shoulder rotator strength and range of motion. Therefore, scapular taping could be recommended for not only in the asymptomatic athletes’ shoulder exercise training but also in the prevention of sub acromial impingement syndrome [17].
Kinesiotape creates pressure on the skin and stretches the skin. By stimulating cutaneous mechanoreceptors, this external loading causes physiological changes in the region where KT was applied. KT increases the distance between skin and muscle and interstitial fluid by increasing the blood and lymphatic circulation [18].
Low level laser was used in treatment of different musculoskeletal problems. The effectiveness of low-level laser treatment was similar to that of local corticosteroid injection in patients with sub acromial impingement syndrome [19].
The bio modulatory effect of LLLT improves local microcirculation and oxygen supply to hypoxic cells in the painful areas. Simultaneously, tissue asphyxia is reduced to a minimum and collected waste products are removed. The laser-induced normalization of microcirculation interrupts the vicious cycle that originates, develops, and maintains pain; in addition, it restores the normal physiological condition of the tissue [20].
Research has shown that LLLT can modulate inflammation by reducing the levels of biochemical markers (prostaglandin E2, messenger ribonucleic acid cyclooxygenase-2, interleukine- 1β, and tumor necrotizing factor-α), neutrophil influx, oxidative stress, edema, and hemorrhage in a dose-dependent manner [21].
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