Specific or general exercise strategy for subacromial impingement syndrome–does it matter? A systematic literature review and meta analysis
- Alison R. Shire†1Email author,
- Thor A. B. Stæhr†1,
- Jesper B. Overby1,
- Mathias Bastholm Dahl†1,
- Julie Sandell Jacobsen1 and
- David Høyrup Christiansen2
© The Author(s). 2017
Received: 7 September 2016
Accepted: 4 April 2017
Published: 17 April 2017
Exercise is frequently suggested as a treatment option for patients presenting with symptoms of subacromial impingement syndrome. Some would argue implementing a specific exercise strategy with special focus on correction of kinematic deficits would be superior to general exercise strategy. There is however a lack of evidence comparing such exercise strategies to determine which is the most effective in the treatment of subacromial impingement syndrome. The aim of this review is to evaluate whether implementing specific exercise strategies involving resistive exercises are more effective than a general exercise strategy for the treatment of patients with subacromial impingement syndrome.
Randomized controlled trials were identified through an electronic search on PubMed/MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials, Web of Science and PEDro. In addition, article reference lists and Clinicaltrials.gov were searched. Studies were considered eligible if they included interventions with resistive specific exercises as compared to general resistance exercise. Four reviewers assessed risk of bias and methodological quality guided by Cochrane recommendations. Results were synthesised qualitatively or quantitatively, where appropriate.
Six randomized controlled trials were included with 231 participants who experienced symptoms of subacromial impingement syndrome. Four studies evaluated the effectiveness of specific scapular exercise strategy and two studies evaluated the effectiveness of specific proprioceptive strategy. Five studies were of moderate quality and one study was of low quality. No consistent statistical significant differences in outcomes between treatment groups were reported in the studies. Standardized mean difference (SMD) for pain was SMD −0.19 (95% CI −0.61, 0.22) and SMD 0.30 (95% CI −0.16, 0.76) for function.
There is insufficient evidence to support or refute the effectiveness of specific resistive exercise strategies in the rehabilitation of subacromial impingement syndrome. More high quality research is needed to accurately assess this. This review provides suggestions on how to improve the methodological design of future studies in this area.
KeywordsImpingement Subacromial Shoulder Physiotherapy Training Function Pain
Subacromial Impingement Syndrome (SIS) is thought to be the most prevalent disorder causing shoulder pain, accounting for up to 50–70% of all shoulder complaints in primary care [1–3]. The term shoulder impingement syndrome was introduced by Neer to describe the pathological state of the rotator cuff tendons resulting from mechanical impingement [4, 5].
Subacromial impingement syndrome is a multifactorial condition where intrinsic and extrinsic mechanisms of rotator cuff pathology are the two main theories underlying SIS aetiology [6, 7]. Intrinsic factors affect tendon morphology and performance over time. These factors are influenced by genetic predisposition, age related changes, poor vascularity, biological alterations and mechanical properties where the physiological limit of the rotator cuff tendon(s) are surpassed [6–8]. Extrinsic factors relate to anatomical structure and/or biomechanical alterations causing mechanical compression [5, 7]. Anatomical structures include variations of the acromion shape as well as osteoarthritic spurs on the subacromial and acromioclavicular joints. Biomechanical alterations refers to the superior translation of humeral head and altered scapulohumeral kinematics often caused by a weakness and imbalance of the rotator cuff musculature and/or tendons opposing superiorly directed shifts as well as postural dysfunction [5, 8–13]. This can present as external impingement with narrowing of the subacromial space or internal impingement within the glenohumeral joint space [6, 8, 13].
Alterations in shoulder kinematics are often observed among patients with SIS [14–20]. The most common documented deficits are alterations in scapulothoracic kinematics [14, 16, 17, 20–26], humeral head displacement within the glenoid cavity [14, 16, 27, 28] and increased elevation and retraction of the clavicle in the sternoclavicular joint during arm elevation [14, 21, 24, 29]. Postural dysfunction relating to increased flexion and kyphosis of the thoracic spine cause alignment impairments which are also said to interfere with shoulder kinematics [16, 21]. These kinematic alterations are suggested to contribute to narrowing of the subacromial space (external impingement) which can affect biceps tendons, rotator cuff tendons, subacromial bursa and subtendinous bursa increasing the risk of joint inflammation and tears associated with SIS [9, 14–16, 19]. Physiotherapists often tailor rehabilitation programs to correct movement deficits, postural dysfunction and or muscles weakness/imbalance in attempted to improve characteristics of the subacromial space [16, 19, 21].
Exercise therapy has shown to reduce pain and improve functional loss associated with SIS, however specific components of exercise protocols are unknown [18, 30–34]. A systematic review from 2012 concluded that a program consisting of multiple types of exercises are effective in the rehabilitation of SIS . These programs consist of a combination of scapular stabilization exercises, rotator cuff resistance exercises, range of motion and stretching exercises. Current evidence is however limited as to the which specific exercise(s) are most effective clinically [32, 35]. However, there is growing evidence to support the use of resistance and proprioceptive exercises over movement based exercises alone [18, 28, 32, 36]. A recent consensus statement from 2013 recommended that scapular kinematic deficits should be addressed with specific exercises in the rehabilitation of SIS . This recommendation included specific exercises strategies aimed to restore normal scapular kinematics by improving the muscle activity, strength, flexibility and balance in muscle force couples that control scapular position and motion [14, 17, 37–39]. In addition, Diedrichsen et al.  suggested that focus on motion awareness and strengthening of the scapular upward-rotators and the rotator cuff should be part of a conservative rehabilitation program for patients with SIS.
An algorithm guideline on rehabilitation of shoulder injuries has been developed . Recommendation for specific rotator cuff and scapular retraining includes muscle activation sequencing, force couple activation, concentric and eccentric control, strength, endurance and avoidance of unwanted movement patterns [18, 40, 41]. Key principles include obtaining flexibility in the muscles to reduce inhibition of activation and execution of specific functional movement or activity [18, 40, 41]. These specific strategies are thought to improve scapular kinematics and thereby ameliorate biomechanical conditions in the shoulder that may reduce symptoms caused by SIS [18, 40, 41]. Despite compelling research on exercise therapy and previous systematic reviews of the effectiveness of different exercise interventions, recently published trials justify an updated systematic review on the effectiveness of specific exercise strategies such as stabilization, positioning, proprioception, neuromuscular control, strengthening, stretching and centering of the humeral head. The aim of this review is to evaluate the outcome differences in treatment of SIS when comparing resistance training programs with and without specific exercise strategy.
The reserach design and methodology for this literature review was based on recommendations from the Cochrane Handbook for Systematic Reviews of Interventions developed by the Cochrane Collaboration .
Criteria for considering studies for this review
Types of studies
Randomized controlled trials (RCTs), published in all languages, investigating any approach of specific exercises in patients with SIS were considered.
Types of participants
Studies were included if participants were older than 18 years and demonstrated the clinical pattern of SIS. Studies were included that, according to examination, had participants presenting with at least one of the following signs of SIS: Pain with overhead activities; painful arc sign; positive Neer impingement test, Hawkins test or Jobes test.
Trials were excluded if they recruited participants with severe injuries including full thickness rotator cuff tears adhesive capsulitis (frozen shoulder), osteoarthritis, fractures/dislocations, neoplasm, systemic inflammatory and autoimmune disorders; infection, neurologic disorders or pain relating to complex neck/shoulder disorders. Postoperative rehabilitation interventions were not considered.
Types of interventions
To be considered for inclusion trials must include resistance exercises in both intervention and control group, and one of the groups must investigate the effect of a specific exercise strategy. Specific exercise strategies can be defined as exercise targeting the activation and coordination of scapulothoracic musculature and/or the dynamic humeral stabilizers that encompass the shoulder joint. Exercise can include scapular stabilization, positioning, proprioception, neuromuscular control, strengthening and stretching. Exercises must involve a form of resistance such as; body weight, elastic resistance, weighted apparatus, weights and/or machine weights.
Types of outcome measures
All outcomes were of interest. The primary outcomes considered were pain and function measured using shoulder-specific scales e.g. Western Ontario Rotator Cuff Questionnaire (WORC) and Shoulder Disability Questionnaire (SDQ). Quality of life (QoL), clinical tests, range of motion (ROM), strength and proprioceptive ability were considered as secondary outcomes.
Search methods for identification of studies
Cochrane Central Register of Controlled Trials (CENTRAL)
Physiotherapy Evidence Database (PEDro)
Web of Science
The search strategy was constructed after consultation with an academic health science librarian. The following index and key free-text terms were used: shoulder, scapula, subacromial, impingement, bursitis, tendinitis, tendonitis, rehabilitation, physiotherapy, physical therapy, exercise and training. All key terms were searched independently and then combined . The search formulas for each database are provided in Appendix 1. Reports not indexed in the databases were manually searched and detected. Furthermore, retrieved articles and systematic reviews were screened for additional relevant publications. A search in clinicaltrials.gov of recent listed studies/unpublished articles was also performed.
Data collection and analysis
Selection of studies
Two review authors (TS, AS) independently applied the inclusion and exclusion criteria to screen the titles and abstracts. Secondly, reviewers (TS, AS) retrieved the potential eligible studies in full-text and evaluated the aim and methods sections for final inclusion. Two other reviewers (JO, MD) compared article selection and resolved any disagreements by consensus. If disagreements persisted, another review author was consulted (DC). All six reviews (TS, AS, JO, MD, DC and JJ) read the eligible studies in full-text and came to an agreement on the six included studies.
Data extraction and management
Two pairs of review authors (AS, MD and TS, JO) independently extracted data from the included studies. Study characteristics regarding methods, participants, interventions, outcomes and results were extracted using standardized data extraction forms in preparation for accurate analysis . Original paper authors were contacted to obtain more information if needed.
Risk of bias assessment
Risk of bias in the included studies was assessed by two independently blinded groups of review authors (AS, MD and TS, JO) and then compared and discussed by all four reviewers.
Any disagreements were resolved by consulting a fifth review author (DC). The level of inter-rater agreement was recorded. Data extraction and evaluation of risk of bias was conducted using Review Manager 5.3 .
Risk of bias was assessed by utilizing the 12 criteria adapted by Cochrane from van Tulder et al. , Boutron et al.  and Furlan et al.  The criteria were used to validate characteristics of the studies that might be related to reporting, selection, performance, attrition and detection bias . A pilot risk of bias assessments was performed with similar articles to ensure consistent interpretation of the criteria between reviewers.
Going from assessments of risk of bias to judgments about study limitations
Risk of bias
Low risk of bias.
Most information is from studies at low risk of bias.
Plausible bias unlikely to seriously alter the results.
No apparent limitations.
No serious limitations, do not downgrade.
Unclear risk of bias.
Most information is from studies at low or unclear risk of bias.
Plausible bias that raises some doubt about the results.
Potential limitations are unlikely to lower confidence in the estimate of effect.
No serious limitations, do not downgrade.
Potential limitations are likely to lower confidence in the estimate of effect.
Serious limitations, downgrade one level.
High risk of bias.
The proportion of information from studies at high risk of bias is sufficient to affect the interpretation of results.
Plausible bias that seriously weakens confidence in the results.
Crucial limitation for one criterion, or some limitations for multiple criteria, sufficient to lower confidence in the estimate of effect.
Serious limitations, downgrade one level
Crucial limitation for one or more criteria sufficient to substantially lower confidence in the estimate of effect.
Very serious limitations, downgrade two levels.
Best evidence synthesis
Levels of Quality
Randomized trials; or double-upgraded observational studies.
Downgraded randomized trials; or upgraded observational studies.
Double-downgraded randomized trials; or observational studies.
Triple-downgraded randomized trials; or downgraded observational studies; or case series/case reports.
Best evidence synthesis guidelines
Provided by consistenta statistically significant findings in outcome
measures in at least two high quality RCTsb
Provided by statistically significant findings in outcome measures
in at least one high quality RCTb
Provided by consistenta, statistically significant findings in outcome
measures in at least two medium quality RCTsb
Provided by statistically significant findings in at least one medium
Provided by consistenta, statistically significant findings in outcome
measures in at least two low quality RCTsb
No or insufficient evidence
If results of eligible studies do not meet the criteria for one of the
levels of evidence listed above (e.g. no statistically significant findings)
In case of conflicting (statistically significant positive and statistically significant negative) results among RCTs
In case of no eligible studies
Data synthesis and analysis
Data analysis was conducted using Review Manager (version 5.3)  of the Cochrane Collaboration and consult of a statistician. Studies were included in the quantitative analysis if the primary outcomes of interest, pain and function, were descriptively comparable at baseline and follow-up in regards to intervention, participants, outcome measures and duration of follow-up. Where possible the means and standard deviations data pain and function of included studies were pooled into a meta-analysis to give the overall summary of effect. Data was converted and calculated to standardized mean difference (SMD) with 95% confidence intervals (CIs) for short term outcomes which ranged from 4 to 8 weeks.
A random effects model was used to determine the overall effect size [42, 51]. An effect size of 0.8 or more was regarded as a large effect size, between 0.5 and 0.8 as a moderate effect size and between 0.2 and 0.5 as a small effect size . Statistical significance was considered at p < 0.05.
Forest plots were used to illustrate effect sizes on pain and function with 95% CIs and to summarize the pooled effect. Funnel plots to identify publication bias were not generated because of the small number of studies available for each analysis. For crossover trials only data from the first period were included . The outcomes measures of pain during movement and function were found comparable across five studies [53–57]. The function scoring scales were reversed in two studies [55, 57] for the adequate interpretation and to enable meta-analysis of the data. To ease interpretation the function scores in two studies were converted to 0–100 [56, 57] and in one study the pain scores were converted to 0–10 .
The degree of heterogeneity was assessed by I2 statistics. The I2 can be interpreted as the proportion of the observed discrepancy in the estimation of the effect, within a group of trials, which cannot be accounted for by random variation . Due to the low number of studies currently available the authors did not restrict the inclusion of studies with high risk of bias. Review authors performed the recommended sensitivity analyses in order to provide a transparent conclusion . The methodological factors such as age, sex, intervention and the follow-up periods of each study were investigated to explore and explain the factors of heterogeneity.
Selection of studies
Characteristics and evaluation of included studies
Baskurt 2011 
Randomized by simple random table.
n = 40, 13 male, 27 female.
24–71 year. with a mean age of 51.
Measured before and after intervention.
Strength: Hand held dynamometer
Function and QoL: WORC.
Clinical tests: Joint Position Sense and Lateral Scapular Slide Test
Patients outcomes improved statistically in both groups (P < 0.05).
No significant difference between groups in all parameters (P > 0.05) except muscle strength for lower trapezius and supraspinatus and clinical tests (P < 0.05).
Comments: Missing P-values and CI in results section. No protocol registered.
Other bias (sample size)
High risk (downgrade 1)
Dilek 2016 
Randomized using block randomization.
n = 63, 21 male, 42 women.
25–65 years. with a mean age of 49.13.
Mean duration of symptoms: approx. 17 months.
Measured at baseline, 6 and 12 weeks.
Strength: Isokinetic dynamometer system (Cybex Norm)
Function and QoL: WORC and ASES
Both groups improved significantly in ROM, pain scores, isometric strength in all angles, Sense of kinesthesia at 0° ER, ASES and WORC (P < 0.05). No significant difference was found between groups in any of the parameters (P > 0.05).
Comments: No protocol registered.
Other bias (sample size)
High risk (downgrade 1)
Martins 2012 
n = 18, nursing professionals with age ranging from 30 to 50+ yrs.
16 subjects completed the study consisting of 2 male and 14 females. (no information on gender n = 2)
Function and QoL: WORC
Both groups exhibited significant reduction in pain scores (P < 0.05), however, no significant differences between groups.
Only the intervention group improved WORC scores significantly.
Comments: Outcomes of pain was less well presented and reduces transparency of data.
Other bias (sample size)
High risk (downgrade 1)
Mulligan 2016 
Randomized using blind draw.
n = 50, 14 male and 26 females, (no information on gender n = 10)
Measured at baseline, 4 weeks, 8 weeks, 16 weeks
Function and QoL: ASES; GPF; GROC.
No significant between group and time. Both groups exhibited significant reduction in pain scores and function. However, no significant differences between groups.
Comments: Protocol registered. Unclear reporting of co-interventions.
Other bias (sample size)
High risk (downgrade 1)
Struyf 2013 
Randomized using closed envelopes.
n = 22, 10 male and 12 females. Aging from 30 to 61 years with a mean age of 45.8.
Measured at baseline, after nine sessions (4–8 weeks) and 12 weeks Post treatment.
Pain:VAS and VNRS
Function and QoL: SDQ
Clinical measures: Strength: handheld
Dynamometer, Impingement test VAS Hawkins, Empty Can or Neer tests. Acromial distance, pectoralis minor length, scapula upward rotation and kinetic medial rotation test.
After nine sessions the Experimental group demonstrated significant effect on self-reported disability compared to the Control group (P = 0.025). Both groups increased from baseline in all outcomes measured (P < 0.05).
No significant differences between group for strength or clinical measures, with exception for VAS by Neers test (p = 0.02)
Comments: The protocol states that outcomes will be measured after 6 months.
It is reported interim analysis was planned, however, is not mentioned in the protocol.
Other bias (sample size and interim analyze)
High risk (downgrade 1)
Wang 2006 
Randomized using pre-prepared sealed envelopes.
n = 38, aging from 26 to 68 years. with a mean age of 44.6. Of the 38 subjects, 30 were analyzed consisting of 15 male and 15 female.
Measured at baseline, 4 and 8 weeks.
Function and QoL: FLEX-SF
Strength: handheld dynamometer
No significant interaction between group and time.
Both groups had significant improvements in regards to pain, function and muscle strength.
FLEX-SF improved significantly after 8 weeks. Pain improved significantly after 4 and 8 weeks.
Comments: No protocol registered. No gender distribution of the included subjects.
Other bias (sample size)
High risk (downgrade 2)
Description of studies
Of the six included studies a total of 231 participants were recruited [53–58]. Gender was reported for 211 participants, 136 women and 75 men; however, one study did not report gender for eight participants , another for two participants  and another for ten participants . Four studies included patients with SIS and used similar clinical diagnosis criteria [53–55, 57]. One study included patients with SIS, but did not describe how diagnosis was made . One study did not clearly address SIS, but rotator cuff disease .
Across the six studies the following outcomes were measured; Pain (at rest, during activity, worst pain during the last 24 h, during night), function and QoL (WORC, American Shoulder and Elbow Surgeons Standardized Assessment Form-self reported scale (ASES), SDQ, Flexilevel Scale of Shoulder Function (FLEX-SF)), strength and ROM [53–58]. Pain was measured using the following instruments; visual analogue scale (VAS), visual numeric scale (VNS), verbal numeric rating scale (VNRS) or Numeric Pain Rating Scale (NPRS) [53–58]. All studies reported function [53–58].
Description of interventions
Two studies had similar intervention groups focusing on specific proprioceptive exercises and centering of the humeral head (positioning) [57, 58], one study compared scapular specific exercises for the shoulder against general resistance exercises  and two studies compared general resistance exercises for the shoulder against the same program with the addition of specific scapular stabilization and neuromuscular control exercises [54, 56]. One study was designed as a crossover trial where each group performed the same specific resistance scapular stabilization and rotator cuff exercises in a different sequence with follow-up at 4, 8, 12 and 16 weeks . For the purpose of this review this study was analyzed at 4 weeks/follow-up before execution of crossover sequence . Two studies reported measurements after the intervention at 4 to 8 weeks  and 6 weeks follow-up . One study reported on 4 and 8 weeks follow-up  and one study reported on 6 and 12 weeks follow-up . The timeframe of follow-up was unclear in one study .
Interventions of all studies lasted between 4 and 8 weeks [53–58], with one study encouraging participants to continue exercise at home for 6 weeks after the intervention . Frequency of interventions varied between trials: Three times per week [54, 57], twice per week , once a day [53, 55] and twice a day . Exercise protocols included: scapular specific and neuromuscular exercises [53–58], strengthening exercises of the shoulder and rotator cuff using gravity, TheraBand™ or free weights as resistance [53, 54, 56–58], stretching and flexibility exercises [54–58], proprioceptive training [54, 57] and general movement exercises [54, 57, 58]. One study selected exercises based on reported high electomyographical activity in target muscle groups .
In summary, all six studies investigated relevant specific exercise strategies over a short term [53–58]; Four studies evaluated the effectiveness of specific scapular exercise strategy [53–56] and two evaluated the effectiveness of specific proprioceptive exercise strategy [55, 57].
Risk of bias assessment and quality rating
The most common methodological deficiency was small sample size. Randomization was performed in all studies. Five studies described random allocation appropriately [53–57]; whereas one study had unclear randomization methods . Another prevalent methodological downfall is the lack of allocation concealment, which was unclear in three out of six studies [53, 54, 56]. The drop-out rate was considered higher than acceptable in one study . All studies analyzed participants by intention to treat principle [53–58]. Selective outcome reporting was of high risk in one study . One study scored unclear for similarity of groups at baseline . Co-interventions were utilized in all studies, but only two were low risk of bias [54, 55]. Four studies failed to report compliance [53–55, 57]. One study failed to address timing of outcome assessment appropriately . This study also failed to specify stopping rules for the performance of their interim analysis contributing to a high risk of bias and a downgrade in evidence quality . All studies had inadequate sample sizes [53–58]. In summary, all studies were deemed to have a high risk of bias [53–58].
Best evidence synthesis
Overall effectiveness of specific exercise strategy and best evidence synthesis across outcomes on short term
Best evidence synthesis
Yes (moderate )
Insufficient (conflicting) evidence
Yes (moderate )
Insufficient (conflicting) evidence
Yes (moderate )
Insufficient (conflicting) evidence
Yes (moderate )
No (low )
aProprioception and clinical tests
Yes (moderate )
Range of motion
All studies investigated the short-term effects of exercise on pain at 4 to 8 weeks follow-up using a range the measurement scales; VAS, VNS, VNRS or NPRS [53–58]. Pain was measured with one or in combination of the following: At rest, at night, with activity, during the last 24 h and/or with function. There was insufficient evidence to support that specific exercise strategies are effective in reducing pain short term. This is consistent with no statistically significant differences between groups in four studies of moderate quality [53, 54, 57, 58] and one study of low quality . In contrast, only one moderate quality study reported a reduction in pain between groups with significant statistical difference .
All studies investigated function of the shoulder using questionnaires to assess short-term symptoms, activities of daily living and QoL experienced among participants with SIS [53–58]. There is insufficient evidence that tailoring a specific exercise strategy can improve function. Three studies of moderate quality utilized WORC, where none of these studies found improvements between groups [54, 57, 58]. Two studies of moderate quality evaluated function using the ASES index and found no effect between groups [53, 57]. One study of low quality evaluated functional status using FLEX-SF and found no difference between groups . The results of one study of moderate quality contradict the results of all other studies by finding a statistical significant improvement between groups when evaluating functional disability status using SDQ .
Four out of six studies investigated isometric strength of the shoulder using hand held dynamometer with different approaches [53–56]; whereas one study used isokinetic dynamometer system . Only one study of moderate quality found a statistical significant difference between groups . Two other studies of moderate quality [55, 57] and one of low quality  found no statistical significant difference. One study only measured muscular strength at baseline .
One study of moderate quality found that implementing specific exercises that focus on scapular stabilization were effective to improve scapular muscles strength with statistical significance between groups . One study of low quality found no difference . Overall, there is limited evidence to support the use of specific exercises to improve scapular muscles strength.
Proprioception and clinical tests
There is conflicting evidence that a specific exercise strategy can improve the clinical outcome measures of proprioceptive ability and shoulder function. Only one study of moderate quality investigated the effectiveness of specific proprioception exercises . Another study of moderate quality implemented specific proprioceptive exercises in their rehabilitation program, however, did not address outcome measures and specify findings between the groups . Two studies of moderate quality focusing on scapular specific exercises provided inconsistent results [54, 55]. These studies were unable to demonstrate an improvement for the clinical outcome measures such as pain provocation test, acromial distance, pectoralis minor muscle length, joint position sense and scapula scapular position and motion [54, 55].
Range of motion
There is no evidence a specific exercise strategy can improve ROM. This is due to insignificant statistical findings between the control and experimental groups in three studies of moderate quality [54, 55, 57], one of which only measured scapula motion and not general shoulder ROM , and one study of low quality . Two studies of moderate quality did not address outcome measures of ROM [53, 58].
Four of the six studies were eligible for inclusion in the statistical pooling for pain [40, 53, 54, 56] and five of the six studies were eligible for function [53–57]. The pooling of data for strength, ROM and clinical tests were deemed inappropriate due to the considerable variation between measurement tools and outcomes used by all the studies. Attempts to contact authors to provide further data were unsuccessful. Overall, the studies included in the meta-analysis were few in number and the true effect sizes varied between studies.
One study measured worst pain in the last 24 h  and one study measured pain during active shoulder elevation . These measurements were assumed to be pain during movement and therefore included for statistical analysis.
One study measured function with ASES and WORC , but only means and standard deviations were reported for the WORC. One study  was excluded for both outcomes as pain was categorized without statistical data and data for function was not provided at baseline and follow-up.
Heterogeneity among the five studies for function outcomes [53–57] can be interpreted as moderate . The amalgamation of the studies into different combinations of three studies [53, 56, 57] and [54–56] resulted in improved heterogeneity (I2 = 0%) illustrated in Additional file 1: Figure S1. The results from the combination of three studies did not favour the use of a specific exercise strategy [53, 56, 57]. In contrast, a moderate effect size was found in favour of specific exercise, when restricting the analysis to three other studies [54–56]. Consequently, the sensitivity analysis for function outcomes provide an unclear conclusion illustrated in Additional files 2 and 3: Figures S2 and S3.
The aim of this review was to evaluate whether implementing specific exercise strategy focused towards the treatment of SIS would result in a superior effect when compared to general exercises strategy in a resistance training program.
Six RCTs were extracted from a systematic search. Five of the studies were of moderate quality [53–55, 57, 58] and one of low quality . All studies implemented a resistive specific exercises strategy in the form of proprioceptive, rotator cuff, scapular and stretching in different combinations. The qualitative results of this review suggest no significant evidence to support the use of specific exercises over general exercises in rehabilitation programs aiming to be an effective treatment for pain, function, ROM and strength in patients with SIS symptoms.
The most common cause for downgrading quality was the lack of adequate sample size which is found in all analyzed studies [53–58]. This increases the probability of inadequate equal distribution of participants with randomization, lack of power, and risk for statistical error . Therefore, the ability to detect statistical significance and derive clinical meaning is reduced lowering overall confidence in the results of all studies .
Limitations such as poor intervention design and description limit transferability of protocols clinically. Unclear randomization  and allocation concealment [54, 56] are both methodological problems that introduce selection bias . Unclear description and dosage of exercise were especially apparent in two of the studies [54, 56]. and in four studies it was unclear whether participants engaged in co-interventions [55–58].
One study had a relatively high drop-out rate which could underestimated efficacy of the intervention . In contrast, applying simple imputation methods such a last observation carried forward, as used in one study , may introduce bias . This could overestimate the efficacy of the intervention, especially if patients only are lost to follow-up in the comparative group. The compliance of participants was unclear in three studies [54, 55, 57], which create uncertainty as to whether the full intervention was received. Compliance is an important component of exercise as a treatment; therefore unclear reporting of compliance can make it difficult to determine true effectiveness. Non-compliance in physiotherapy interventions is as high as 70% . Education for the rationale and perseverance of an exercise programs may be beneficial for both patient compliance and outcome measures .
The crossover design in one study employed the same intervention in both groups with different temporal sequence . Regardless of the exercise type and sequence, both exercise strategies contributed to improvements in pain and function experienced by the subjects .
Most assessment tools utilized by included studies were valid and reliable for assessing outcomes measures among shoulder patients [53–58, 60, 61]. However, the reliability for strength, ROM and other clinical tests can be challenged and discussed. The variability of the clinical assessments/measures for function created methodological diversity among included studies. The tests used to assess strength, ROM and proprioception with scapular-specific tests in two studies [54, 55] are questionable as outcome measures for assessing the shoulder. There is a lack of validity and reliability which limit the clinical value of these tests [25, 60–62].
The results from the quantitative analysis for the primary outcomes of interest pain and function favour specific exercise strategies; however there was no significant statistical evidence proving them as a superior treatment.
Analyses of the heterogeneity among the studies revealed that inclusion and/or exclusion of one study  pulled results in different directions. For analysis of specific exercise strategies on pain the combination of three studies [53, 54, 56] resulted in zero heterogeneity and a small effect size not in favour of specific exercises. For function the combination of three studies resulted in zero heterogeneity and a moderate effect size [54–56]. It is difficult to pinpoint precisely which factors influence this variation of heterogeneity and as to why different combinations of studies result in a change of effect size. This reduces the clinical significance of the result. Disparity of clinical measures across all studies may be one factor contributing to the variation of heterogeneity. The deciding study  pulling results towards an effect of intervention presents methodological shortcomings when assessed using the Cochrane handbook and CONSORT criteria [42, 48]. Speculation of poor methodology and interventions cannot be dismissed and care should be taken when drawing conclusions estimating effect .
Attempts were made to improve the quality of evidence by pooling data from the eligible included studies for the quantitative analysis of pain and function. This however did not strengthen the results of this review and the conclusion remained affected.
Furthermore, all included studies were of high risk of bias and although this was addressed with sensitivity analysis strategies the inclusion of these studies in a meta-analysis lower the quality of evidence and power of this review . Overall, this prevents a firm conclusion to support the use of specific exercises in clinical practice.
Comparison with previous literature
Two previous systematic reviews investigated scapular-focused treatment strategies including; scapular-exercise, mobilisation techniques and taping in patients with subacromial pain syndrome and found insufficient evidence to support for the use of scapular-focused treatment [63, 64].
Similar to the results of this present review, both previous reviews found significant methodological limitations among the available evidence [63, 64]. One review  found the literature not to be supportive of different scapular-focused treatment approaches for pain and function; All studies investigated the short-term effects of exercise on pain at 4 to 8 weeks follow-up; whereas the meta analysis of one review found statistical, but not clinically relevant benefit for the use of scapular-focused treatment in the short term function . These previous reviews have limited value for assessing the effectiveness of exercise as the exercises identified focused on scapular position and movement disregarding evidence that resistive exercises are superior [18, 28, 32, 63, 64]. Moreover, these previous reviews lack investigation of proprioceptive exercise protocols which, in the review authors’ opinion, is an important aspect of specific exercise strategy in rehabilitation programs aimed at correction of movement and kinematics.
In contrast to previous reviews, this is the first systematic review specifically examining effectiveness of specific resistive exercises compared with general exercise in the rehabilitation of patients with SIS.
One previous systematic review evaluate the role of exercise in treating rotator cuff impingement and found a strong suggestion that exercise improves symptoms in patients with SIS . This review included exercise programs with components of home-exercises, manual therapy and other modalities  and therefore does not provide evidence supporting specific exercises as more effective then general exercise interventions.
Previous recommendations from a consensus statement, which supported the use of scapular rehabilitation protocols within a comprehensive program to potentially improve scapular muscle strength, shoulder symptoms and alter scapular position , are not supported by the results of this review.
A small number of studies were found comparing the use of specific resistive exercise with movement-based exercises without external resistance in rehabilitation of SIS and were deemed unfit for inclusion [28, 40, 65–67]. Furthermore, other reviews offer evidence that resistance training of any type is superior to movement based training only [16, 18, 30, 32, 68]. Therefore, it would be difficult to determine effectiveness of specific exercise from these studies. One excluded study tested the effects of a neurocognitive approach compared to traditional therapeutic exercises in patients with SIS , and found the neurocognitive approach to result in larger improvement in shoulder function and pain . Interestingly, the traditional therapeutic exercise group engaged in specific resistive exercises which focused on the rotator cuff and scapular stabilizing muscles . These findings could indicate the need for consideration of different styles of intervention for the treatment of SIS patients.
There is currently one completed upcoming RCT that, with reference to the protocol registration at clinicaltrials.gov, could meet inclusion criteria of this review (Elif Turgut NCT02286310) (Appendix 3). The protocol description includes specific exercise therapy for patients with SIS and scapular dyskinesia only, however the results of this upcoming RCT could be considered in future investigations of specific exercise strategy.
Two recent Cochrane systematic reviews evaluating the use of the motor control as a specific exercise strategy among low back  and neck pain populations . Both studies suggest specific motor control exercises, aimed at restoring control and coordination of deep stabilizer muscles of the spine, were not superior to more general exercise strategies [69, 70]. Both studies conclude no single exercise strategy is superior to another [69, 70]. In comparison to the results of this present review similar conclusions could be drawn for the use of specific exercises such as scapulothoracic, positioning, proprioceptive and neuromuscular control exercises for the treatment of SIS.
Strengths and limitations
As suggested by Cochrane, reviewers conducted a wide systematic search strategy with high sensitivity and low precision in order to detect all relevant articles . Despite a comprehensive search process, reviewers collected only six articles suitable for inclusion [53–58]. A limited number of studies of moderate to low quality may have contributed to an over or under estimated effect and thus prevents any clear conclusions. Moreover, there are a relatively low number of participants in this review and it should be noted that high quality RCTs with adequate sample sizes might change the estimate of effect. Wang et al.  did not clearly state the inclusion of participants with SIS. It could be argued that this study did not meet inclusion criteria and therefore excluded. One study could not be included in statistical pooling for both pain and function as the presentation of the results limited data extraction .
However, excluding this study would not have changed the overall results and conclusion of this review. Limitations such as the unclear definition of SIS combined with the multifactorial nature of SIS could affect the results of this review [6, 7, 60, 61]. To ensure quality the authors underwent several pilot-tests regarding risk of bias assessment and data extraction. Moreover, reviewers conducted this review based on guidelines from credible sources [42, 48, 71].
Implications for practice
Despite compelling research on exercise therapy there is insufficient evidence to either support or disprove specific exercises strategies for treatment of patients with SIS.
Due to inconsistencies and lack of high quality among the available evidence, this review is unable to demonstrate whether implementing specific exercises in a rehabilitation program for patients with SIS is relevant for clinical practice. Furthermore, no recommendations about nature of exercises, frequency, dose and intensity can be made.
Implications for further research
Future studies aiming to investigate specific exercise strategies should aim to minimize potential bias by presenting a clear methodological design for method of randomization, allocation concealment, blinding etc. This includes a clear description of inclusion criteria, criteria for diagnosis of SIS, reproducible and transparent interventions and co-interventions. There is a need for studies with larger sample sizes to ensure adequate power to detect small inter-group differences. Moreover, follow-up schemes over 6 months will aid to determine long-term effects of the intervention.
If future trials find specific exercises to be effective for the treatment of SIS, a dose-response effect is needed to guide clinical practice in regards to frequency, intensity, dosage (sets/repetitions), rest, tempo manipulation, and whether programs should be individualized or standardized.
Author Alison R. Shire
Author David Høyrup Christiansen
Author Jesper B. Overby
Author Mathias Bastholm Dahl
Quality of life
Randomized controlled trials
Range of motion
Shoulder Disability Questionnaire
Subacromial impingement syndrome
Standardized mean difference
Author Thor A. B. Stæhr
Visual analogue scale
Verbal numeric rating scale
Visual numeric scale
Western Ontario Rotator Cuff Questionnaire
For their support during the review process:
Trine Marlene Nedergaard Jensen, VIAUC, Campus Aarhus N
Michelle Fitzgerald, BSc, MSc, Tallaght Hospital, Ireland
Birte Stæhr Juul, MD, PhD Denmark
Vivian Leite, BSc OT, Perth, Australia
No funding was received. The authors certify that they have no affiliations with or financial involvement in any organization or entity with a direct financial interest in the subject matter or materials discussed in the article.
Availability of data and materials
Not applicable. This manuscript does not contain any data. Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.
All authors planned and designed the study. AS, JO, TS, MD, conducted the litterateur search, selection of studies, extraction of data and risk of bias assessment supervised by DC and JJ. DC and JJ also revised the manuscript critically for important intellectual content. AS and TS drafted the manuscript. All authors contributed to interpretation of findings and critical revision of the manuscript. All authors have participated sufficiently in the work to take public responsibility for appropriate portions of the content; and agreed to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All authors have read and approved the final manuscript to be published. DC, TS and AS conducted the meta analysis and contributed to the acquisition, analysis and interpretation of data. All authors have read and approved the final manuscript to be published.
The authors declare that they have no competing interests. No financial and non-financial competing interests.
Consent for publication
Not applicable. This manuscript does not contain data from any individual person.
Ethics approval and consent to participate
Not applicable. This manuscript does not report on or involve the use of any animal or human data or tissue.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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