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Ann Rehabil Med > Volume 44(5); 2020 > Article
Kamel, Basha, Alsharidah, Hewidy, Ezzat, and Aboelnour: Efficacy of Extracorporeal Shockwave Therapy on Cervical Myofascial Pain Following Neck Dissection Surgery: A Randomized Controlled Trial



To investigate the efficacy of extracorporeal shockwave therapy (ESWT) on cervical myofascial pain following neck dissection in reducing pain and improving cervical range of motion (ROM).


Forty-six patients with cervical myofascial pain following neck dissection surgery were recruited and subdivided at random into two equal groups. The ESWT group received ESWT once a week for 4 weeks (0.25 mL/mm2, 1,000 shocks) and a topical non-steroidal anti-inflammatory drug (3 times/day for 4 weeks). The control group received only topical NSAID. The pain assessment was done by using the visual analog scale (VAS) and pressure algometry. A cervical ROM device was used for the assessment of the lateral flexion and rotation of the neck ROM on both sides. All measurements were collected at baseline, 2 weeks, and 4 weeks.


The ESWT group revealed a significant improvement in all parameters at post I and post II than did the control group (p>0.001), that revealed a statistical decrease only in the VAS score at post I without any statistical difference in the pain threshold and neck ROM. However, there were statistical differences in all parameters at post II compared to those at pre-treatment and post I (p<0.001).


As a confirmation of the efficacy of ESWT in cervical myofascial pain control following neck dissection, we observed better results with no side effects in the ESWT group (Clinical Trial Registry No. PACTR202002648274347).


The surgical dissection of the neck is a typical technique for the management of head and neck malignant growths from the squamous cell carcinoma [1]. There are various approaches to performing the neck dissection surgery. It is worth noting that each surgical approach involves different anatomical structures and has associated postoperative side effects. One of these approaches is the radical neck dissection that involves the total excision of lymph nodes from one side of the neck, the muscle that helps turn the head (sternocleidomastoid muscle), a significant vein (internal jugular vein), and a nerve that is essential in the full-range of movement of the arm and shoulder (spinal accessory nerve). In contrast, the modified radical neck dissection preserves one or more of the aforementioned important structures [2,3]. Furthermore, selective neck dissections are performed to preserve important anatomical structures, while safely excising cancerous lymph nodes from the neck tissues on the affected side [3]. Morbidities related to neck and shoulder surgeries for head and neck cancer treatment are a major point of concern. Van Wilgen et al. [4] showed that shoulder and neck pain can affect the patients’ quality of life at least one year following neck dissection. Early postoperative complications include infection, thrombosis, chyle leak, and cardiac problems. The most widely recognized late complications include neck pain and stiffness, limited shoulder and cervical range of motion (ROM), lymphedema, a reduction in mouth opening, and swallowing difficulty. While a radical neck dissection produces the greatest changes in neck and shoulder function, a selective neck dissection produces the least [5].
The incidence of neck morbidity following cancer treatment was significant and prominent including neck pain, the lack of sensation, and restricted ROM [4]. In an investigation of 25 patients with permanent neck pain following neck dissection, two types of neck pain were described; neuropathic and myofascial pains [6]. Moreover, in 220 patients who underwent neck dissection surgery, neck and shoulder pains were observed in 33% and 37% of the patients, respectively, while neuropathic and myofascial pains were observed in 32% and 46%, respectively [4].
Myofascial pain syndrome (MPS) is a common musculoskeletal disorder characterized by an intensive and deep pain in one or more muscles and fasciae besides muscle tightness, tender points, limited ROM, fatigue, weakness and occasionally autonomic dysfunction [7,8]. MPS can be diagnosed by using pressure algometry for pain threshold evaluation [9]. Physical examination yields a palpable intramuscular band tension, muscle tenderness, and trigger points causing localized or referred pain [10]. Myofascial pain can be managed pharmacologically using non-steroidal anti-inflammatory drugs, antidepressants, anticonvulsants, and muscle relaxants; and non-pharmacologically using dry needling, trigger point injection (TPI), transcutaneous electrical nerve stimulation (TENS), and ultrasound (US) [11].
Extracorporeal shockwave therapy (ESWT) has been introduced efficiently for more than 20 years as a treatment modality in orthopedic and musculoskeletal disorders such as plantar fasciitis, calcific tendinitis, non-union of bone fractures, and epicondylitis [12-14]. ESWT has mechanical and cellular impacts on tissue regeneration and pain management through cavitation bubbles, acoustic microstreaming, and hypervascularity that can directly affect tissue calcifications, thereby modulating cell activity. Pain management can be achieved by blockage of the gate control mechanism through firing of the large sensory nerve fibers (Aβ fibers) in the affected site, which in turn inhibits pain through GABAergic interneurons in the dorsal horn. The vicious cycle of MPS (pain–spasm– ischemia–pain) can be inhibited by the mechanical resolution of persistent sarcomere contractures, through the localized stretching of the sarcomeres by applying shockwaves vertical to the fiber alignment until the abnormal sarcomere knots are destroyed. The energy generated during the process, excessive tissue perfusion, and angiogenesis can reduce the resultant ischemia to eliminate vasoneuroactive substances released by the pressure applied on the tissue [14-25].
Minimal evidence exists regarding the efficacy of ESWT on MPS after surgery; therefore, this study strived to examine the efficiency of ESWT as a mono physiotherapeutic modality in MPS management following a neck dissection surgery, in term of improving pain and cervical ROM. This study may provide a safe, effective and noninvasive treatment modality for MPS, in an attempt to avoid invasive modalities and oral medications that cannot be tolerated for a long period due to their systemic adverse effects.



Forty-six patients diagnosed with cervical MPS following a neck dissection surgery were referred to our outpatient clinic from the National Cancer Institute, Cairo University, and participated in this study. The diagnosis of MPS was done by an orthopedic specialist according to Simons’ criteria [26], where five major criteria and a minimum of one to three minor criteria are required to confirm diagnosis. The major criteria were: (1) localized neck pain, (2) pain or altered sensation within the anticipated allocation of referred pain from myofascial tender points, (3) patients with palpable intramuscular taut bands, (4) oversensitive spot tenderness at one point on the length of the tense band, and (5) restriction in cervical ROM. The minor criteria were: (1) provocation of the clinical symptoms through active trigger point compression, (2) the presence of a local twitch reaction by snapping the trigger point or inserting a needle inside the trigger point within the tense band, and (3) pain relief by muscle lengthening or stretching.
Patients were enrolled in the trial if they met the following criteria: (1) age ranging from 35–60 years, (2) previous unilateral modified radical neck dissection, (3) a history of MPS involving upper trapezius for at least 3 months, and (4) moderate to severe pain (VAS score >4). The exclusion criteria were: (1) patients who received medication or other therapies for MPS within the previous 2 months, (2) the presence of a pacemaker, (3) pregnancy, (4) a wound in the affected area, (5) a cervical disk lesion, myelopathy or radiculopathy, (6) a cervical spine fracture or spondylolisthesis, (7) rheumatoid arthritis, (8) coagulopathy, and (9) epilepsy or any psychological disorders.

Sample size determination

Pre-trial sample size computation was done via G*Power statistical software (version;—F tests, MANOVA (repeated measurements and between factors), α=0.05, β=0.2, Pillai V=0.16, and large effect size, revealing the convenient sample size to be n=46 [27].


This trial was a single-blinded randomized controlled experimental study and was assented by the Ethical Committee of the Faculty of Physical Therapy, Cairo University (No. P.T.REC/012/001857). The study was retrospectively registered in the Pan African Clinical Trials Registry (No. PACTR202002648274347). All aspects of the study were disclosed and informed consent was obtained. The patients were randomly assigned into two equal groups via the envelope mode. After patients’ agreement to participate in the study, cards with either “ESWT” or “topical diclofenac gel” recorded on them were closed in envelopes; then a blinded physical therapist was asked to select one envelope. According to the selected card, patients were assigned to their corresponding group. Dates for starting the allocated therapy were regulated and the therapy was begun after the first week of randomization. The examiner physical therapist was not included in randomization procedures and was unaware of the therapy allocation. Patients were asked not to disclose their therapy allocation to the physical therapist during assessment. The participants were informed to report any harmful effects throughout the treatment period.

Assessment methods


The VAS was used for assessing and quantifying pain exhibited by the patients through a 0–10 scale. Each subject was informed to mark the line according to the pain intensity experienced at that particular time where 0 means no pain and 10 means worst conceivable pain.

Cervical ROM assessment

The cervical ROM device (CROM; Performance Attainment Associates, Lindstrom, MN, USA) was used for the assessment of the neck lateral flexion and rotation on both sides. The CROM instrument contains a plastic frame put on the head above the nose and ears, attached to the occiput by a Velcro strap to allow for precise measurement, and it eliminates individual errors. Two independent inclinometers were connected to the frame and pointed the head position in relation to the gravity line. Another inclinometer indicated the head position in rotation in relation to a reference position.

Pressure pain threshold assessment

A pressure algometer (Somedic AB, Farsta, Sweden) was used for pressure pain threshold (PPT) assessment on the trigger spots. It contains a rubber disk (1 cm2 surface), attached to a pressure pole and inserted into a gauge, for recording the pressure in kilograms. Participants were informed to elucidate when the pressure sensation became painful and to immediately release the pressure. The most painful point on the upper trapezius, as reported by the patient and investigated by the algometer, was selected for PPT measurement. This point was marked by a waterproof marker on the initial visit. The average of three measurements was recorded.


Both groups received 1% topical diclofenac gel on the tender points 3 times/day for 4 weeks. The experimental group additionally received ESWT (Duolith SD1 device; Storz medical, Tagerwilen, Switzerland) with the following parameters: 1,000 shocks; energy flux density (ED) of 0.25 mL/mm2, on the trigger point area, once a week for 4 weeks. All patients were instructed not to take any other medicaments for MPS during the treatment period. All patients were evaluated at baseline, and on the 2nd and 4th weeks after initiation of therapy.

Statistical analysis

Characteristics between groups were evaluated using the descriptive and t-test, while comparing of gender and affected side distribution was done by the chi-squared test. Shapiro-Wilk test was applied for all variables for checking of normal data distribution. Homogeneity testing between groups was done by Levene’s test. The comparison of the treatment impacts on rotation and side bending, ROM, VAS, and PPT within and between the groups was done by the mixed MANOVA. Partial etasquared was deemed as the effect size. Post-hoc tests utilizing Bonferroni correction were used for various subsequent comparisons. The significance level of all measurable tests was set at p<0.05. All statistical analyses were applied by the Statistical Package for the Social Studies (SPSS) version 22 for Windows (IBM, Armonk, NY, USA).


Fig. 1 details the process of patient randomization in this study. Fifty-one participants were admitted and examined for eligibility; 5 of them were excluded as they did not fulfill the required criteria, whereas 46 subjects were found to be qualified to partake in the trial. Forty-three patients went through the treatment program, while 3 patients withdrew because of cancer recurrence.

Subject characteristics

The meanstandard deviation of subjects’ characteristics in both groups are illustrated in Table 1. There were no statistical differences (p>0.05) in the age, weight, height, sex distribution, time from surgery, onset of pain, and diagnosis for surgery between groups.

Effect of treatment on rotation and side bending ROM, VAS, and PPT

Mixed MANOVA showed a significant interaction between treatment and time (Wilks’ λ=0.01, F(12, 30)=227.55, p=0.001, η2=0.98). There was a significant main effect of time (Wilks’ λ=0.005, F(12, 30)=489.27, p=0.001, η2=0.99). There was a significant main effect of treatment (Wilks’ λ=0.03, F(6, 36)=162.55, p=0.001, η2=0.96). Tables 2 and 3 showed the descriptive statistics of rotation and side bending ROM, VAS, and PPT; and the statistical level of comparison between groups; as well as significance level of comparison between pre, post I, and post II in each group.

Between group comparisons

A significant increment of neck rotation, and side bending ROM in both directions away and toward the operated side with a marked improvement of PPT was reported at post I and post II in the ESWT group compared to the control group (p>0.001). Moreover, there was a significant decrease in VAS in the ESWT group at post I and post II compared to the control group (p>0.001).

Within group comparison

Statistical improvements were noted in the rotation and side bending ROM in both directions away and toward the operated side, and also in the PPT in the ESWT group at post II in comparison with the pre-treatment and post I (p<0.001); furthermore, there was a significant amelioration in the rotation and side bending ROM in both directions, and the PPT at post I compared with that of pre-treatment (p<0.001). There was a statistical diminution of the VAS score in the ESWT group at post II compared to pre-treatment and post I (p<0.001); and also, in the VAS score at post I in comparison with pre-treatment (p<0.001).
There was no statistical difference in the rotation and side bending ROM in both directions and in the PPT between pre-treatment and post I (p>0.05) in the control group; however, there was a statistical increase in the rotation and side bending ROM in both directions and also in the PPT at post II in comparison with pre-treatment and post I (p<0.001). There was a statistical decrease in the VAS score in the control group at post II compared with that at pre-treatment and post I (p<0.001); as well as in the VAS score at post I in comparison with pre-treatment (p<0.001).There were no adverse effects reported during the trial.


ESWT has been known as one of the most effective modalities for different musculoskeletal disorders including tendinitis, plantar fasciitis, chronic pelvic pain and rotator cuff disease [28]. In this study, a significant increase in neck rotation was noted in the ESWT group as the percentage changes in neck rotation away from and toward the operated side were 15.8% and 13.05% at post I and increased to 24.95% and 22.85% at post II, respectively. A significant increase in side bending was reported as the percentage changes in side bending away from and toward the operated side were 11.35% and 10.63% at post I and increased to 27.99% and 25.04% at post II, respectively. The PPT and VAS score assessments showed significant improvements as the percentage of perceived pain was decreased by 41.07% and 42.47% at post I and changed to 77.85% and 72.74% at post II, respectively. These outcomes may be due to the vertical mechanistic energy of ESWT applied to the firmly connected actinmyosin; furthermore, pain alteration may occur via the release of substance P and nitric oxide.
ESWT has been evaluated in several different studies, and Ji et al. [29] evaluated a total of 4 sessions of ESWT (0.056 mJ/mm2, 1,000 impulses, twice/week) in patients with MPS in the upper trapezius. The assessment by the VAS score and pressure algometry showed a significant difference as the percentages of improvement of the VAS score and PPT were 53.76% and 51.48%, respectively. On the other hand, Jeon et al. [30] evaluated the aforementioned parameters in 3 sessions of ESWT (0.10 mJ/mm2, 1,500 pulse, one session per week) and reported 72.88% and 83.23%, respectively. Park et al. [31] compared different energy levels of ESWT (0.210 mJ/mm2 vs. 0.068 mJ/mm2, 1,500 pulses, one session a week for 2 weeks) in 30 patients with MPS of the upper trapezius. The percentages of improvement of the VAS score and PPT at a higher intensity were 47.08% and 42.33%, respectively, and 43.14% and 22.75%, respectively, at a lower intensity.
The results of the previous studies support the findings of this study, reflecting significant improvement in pain intensity and threshold, the similarity between past studies and this study is using focused ESWT and the same methods of assessment, nevertheless, there is difference in the outcomes, the reason for this is not clear, it may be as a result of using different energy level in each study, another possible explanation for these results may be the lack of standardized ESWT parameters used for MPS management. Moreover, the previous studies evaluated ESWT on primary MPS, unlike this study which assessed MPS secondary to neck dissection surgery.
Gur et al. [32] compared one to three sessions of ESWT (0.25 mJ/mm2, 1,000 impulses) in 64 patients with MPS of the trapezius muscle. The assessments of pain, quality of life, and trigger points count showed significant improvements in both groups, while higher results were observed in the group receiving 3 sessions. In another study, the same authors evaluated 3 sessions of the same ESWT parameters versus 10 sessions of US in 66 patients with MPS in the trapezius using the previous methods of assessment. The results showed the efficacy of both modalities in MPS with a superiority of ESWT outcomes in pain management [33]. There are similarities between the two aforementioned studies and our study in terms of the ESWT parameters used; however, our study differs from theirs in that objective assessment methods were used in ours, unlike in theirs. Notwithstanding, the results of these studies coincided with our results as far as the efficacy of ESWT in pain management was concerned.
Furthermore, Hong et al. [34] made a comparison between 3 sessions of ESWT (0.085–0.148 mJ/mm2, 2,000 impulses) and 3 sessions of TPI in quadratus lumborum using the VAS score and digital algometer for pain assessment. Both treatments showed significant improvements in the VAS score and pain threshold (65% and 39.18% vs. 44.12% and 10.39%, respectively). However, the ESWT achieved better results and was superior to TPI suggesting it is a more effective modality for MPS treatment. From all the previous studies, it can be concluded that efficiency of ESWT in MPS management is based on the underlying mechanism of ESWT in decreasing the level of muscle tension and the amelioration of localized ischemia in the regions of abnormal muscles shortening. Hence, it prevents the increase in metabolism and onset of an energy crisis, thereby allowing muscle relaxation which in turn increases muscle length and permits a free ROM. In addition, the ESWT eliminates the release of different pain inducing substances, and prevents pain induction caused by the extra excitation of nociceptors of muscles and the selective destruction of non-myelinated fibers.
In this study, better statistical results were reported in VAS, PPT, and neck ROM of the ESWT group than in the control group (p>0.001). However, this study was limited by a small sample size and the absence of shoulder pain and ROM assessments which could provide better statistical analyses. Further researches are recommended with larger sample sizes to evaluate and assure the efficacy of ESWT in MPS and to examine different intensities and frequencies in an attempt to reach the optimal doses in musculoskeletal disorders, as the absence of definite guidelines for ESWT standardized parameters is also considered a limitation. Also, the efficacy of the ESWT in improving the result measures are surmised exclusively depending on the past evaluation; hence, additional histological and molecular studies ought to have been conducted along with the current evaluation. Lack of previous studies on the impacts of ESWT on postsurgical myofascial pain is another limitation. We, therefore, recommend further studies to investigate the effects of shockwaves on MPS after different surgeries. Follow-up studies are also required to reveal ESWT effects in the long run.
In conclusion, ESWT is an effective and safe treatment modality for cervical MPS following neck dissection. These results demonstrated that ESWT could be an alternative treatment for cervical MPS following neck dissection.


No potential conflict of interest relevant to this article was reported.


Conceptualization: Aboelnour NH, Kamel FH, Basha M, Ezzat M. Methodology: Aboelnour NH, Ezzat M. Formal analysis: Kamel FH, Basha M, Aboelnour NH, Hewidy IM. Funding acquisition: None. Project administration: Aboelnour NH, Ezzat M. Visualization: Aboelnour NH, Kamel FH, Basha M, Hewidy IM. Writing - original draft: Aboelnour NH, Kamel FH, Basha M, Hewidy IM. Writing - review and editing: Hewidy IM, Ezzat M, Alsharidah A. Approval of final manuscript: all authors.

Fig. 1.
Participants’ flowchart. ESWT, extracorporeal shockwave therapy; VAS, visual analog scale; ROM, range of motion; CROM, cervical range of motion.
Table 1.
Basic characteristics of all participants
Characteristic Study group Control group p-value
Age (yr) 48.8±7.5 50.8±6.3 0.35
Weight (kg) 84.1±3.7 83.4±3.3 0.48
Height (cm) 173.9±4.4 174.2±2.9 0.80
Time since surgery (mo) 13.13±1.28 13.28±1.34 0.71
Onset of pain (mo) 6.27±1.03 6.58±1.08 0.44
Sex 0.55
 Male 7 (32) 5 (24)
 Female 15 (68) 16 (76)
Affected side 0.42
 Right 18 (82) 15 (71)
 Left 4 (18) 6 (29)
Diagnosis for surgery 0.37
 Oral/oropharynx 10 (46) 7 (33)
 Larynx/hypopharynx 8 (36) 12 (57)
 Thyroid 4 (18) 2 (10)

Values are presented as mean±standard deviation or number (%).

Table 2.
Mean rotation and side bending ROM pre, post I, and post II of study and control groups
ROM (°)
Pre Post I Post II Pre vs. post I Pre vs. post II Post I vs. post II
Rotation away from operated side Study group 61.22±1.74 70.90±1.74 76.50±1.40 0.001* 0.001* 0.001*
Control group 60.95±1.43 61.33±1.39 64.00±1.51 0.79 0.001* 0.001*
p-value 0.57 0.001* 0.001*
Rotation toward operated side Study group 63.04±1.58 71.27±1.85 77.45±1.53 0.001* 0.001* 0.001*
Control group 62.38±1.60 62.80±2.00 65.00±1.94 0.74 0.001* 0.001*
p-value 0.17 0.001* 0.001*
Side bend away from operated side Study group 30.04±1.25 33.45±1.10 38.45±0.67 0.001* 0.001* 0.001*
Control group 30.42±0.97 30.85±1.31 32.381.28 0.34 0.001* 0.001*
p-value 0.27 0.001* 0.001*
Side bend toward operated side Study group 31.22±1.02 34.54±1.14 39.04±0.72 0.001* 0.001* 0.001*
Control group 31.38±1.24 31.71±1.05 33.14±0.96 0.17 0.001* 0.001*
p-value 0.66 0.001* 0.001*

Values are presented as mean±standard deviation.

ROM, range of motion.

* p<0.05.

Table 3.
Mean VAS and PPT pre, post I, and post II of study and control groups
Pre Post I Post II p-value
Pre vs. post I Pre vs. post II Post I vs. post II
VAS Study group 6.31±0.77 3.63±0.58 1.72±0.63 0.001* 0.001* 0.001*
Control group 6.14±0.91 4.47±0.92 3.04±0.86 0.001* 0.001* 0.001*
p-value 0.5 0.001* 0.001*
PPT (kg) Study group 2.80±0.22 3.95±0.25 4.98±0.37 0.001* 0.001* 0.001*
Control group 2.87±0.21 2.91±0.24 3.17±0.24 0.28 0.001* 0.001*
p-value 0.36 0.001* 0.001*

Values are presented as mean±standard deviation.

VAS, visual analog scale; PPT, pressure pain threshold.

* p<0.05.


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