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CRE0010.1177/0269215517732820Clinical RehabilitationLaimi et al.

CLINICAL
Original Article REHABILITATION

Clinical Rehabilitation

Effectiveness of myofascial 1­–11


© The Author(s) 2017
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DOI: 10.1177/0269215517732820
https://doi.org/10.1177/0269215517732820

chronic musculoskeletal pain: journals.sagepub.com/home/cre

a systematic review

Katri Laimi1, Annika Mäkilä1, Esa Bärlund2, Niina


Katajapuu2, Airi Oksanen1, Valpuri Seikkula1,3, Jari
Karppinen3 and Mikhail Saltychev1

Abstract
Objective: To evaluate the evidence on the effectiveness of myofascial release therapy to relieve chronic
musculoskeletal pain and to improve joint mobility, functioning level, and quality of life in pain sufferers.
Data sources and review: Randomized controlled trials were systematically gathered from CENTRAL,
Medline, Embase, CINAHL, Scopus, and PEDro databases. The methodological quality of articles was
assessed according to the Cochrane Collaboration’s domain-based framework. In addition, the effect sizes
of main outcomes were calculated based on reported means and variances at baseline and in follow-up.
Results: Of 513 identified records, 8 were relevant. Two trials focused on lateral epicondylitis
(N = 95), two on fibromyalgia (N = 145), three on low back pain (N = 152), and one on heel pain
(N = 65). The risk of bias was considered low in three and high in five trials. The duration of therapy
was 30–90 minutes 4 to 24 times during 2–20 weeks. The effect sizes did not reach the minimal
clinically important difference for pain and disability in the studies of low back pain or fibromyalgia. In
another three studies with the high risk of bias, the level of minimal clinically important difference was
reached up to two-month follow-up.
Conclusion: Current evidence on myofascial release therapy is not sufficient to warrant this treatment
in chronic musculoskeletal pain.

Keywords
Myofascial release, systematic review, chronic pain, musculoskeletal disorders, manual therapy

Date received: 20 February 2017; accepted: 30 August 2017

1Department of Physical and Rehabilitation Medicine, Turku Corresponding author:


University Hospital and University of Turku, Turku, Finland Katri Laimi, Department of Physical and Rehabilitation
2Turku University of Applied Sciences, Turku, Finland Medicine, Turku University Hospital and University of Turku,
3Department of Expert Services, Turku University Hospital PO Box 28, FI-20701 Turku, Finland.
and University of Turku, Turku, Finland Email: katri.laimi@tyks.fi
2 Clinical Rehabilitation 00(0)

Introduction chosen treatment reaches only statistical signifi-


cance or also the minimal clinical importance. It is
Chronic musculoskeletal pain imposes a substantial not known either whether the therapeutical effect of
burden on healthcare systems and is a common cause myofascial release is long enough to justify the use
of deteriorated daily functioning and quality of life.1 of this treatment in a chronic pain situation.
Among therapies suggested for managing such pain The objective of this study was to evaluate the
is myofascial release—a rapidly spreading form of evidence on the effectiveness of myofascial release
manual therapy aiming pain relief by restoring therapy to relieve pain and to improve joint mobil-
impaired functions of soft tissues. The theory behind ity, functioning level, and quality of life among
therapeutic effects of myofascial release is based on patients with chronic musculoskeletal pain.
the special role of connective tissue sheets—
“fascia”—as a main factor determining musculoskel-
etal system functioning.2 According to that theory, Literature search methods
fascial system, as spreading from head to toe, may Search criteria
behave like an organ with different functions and
capabilities making a major contribution to the Criteria for considering studies for this review were
dynamic properties of the body.2,3 Tightened or stiff- based on PICO framework (Population, Intervention,
ened fascial tissue or its reduced sliding ability (due to Comparison, and Outcome) as follows:
either repeated micro-trauma or acute injury) is
thought to be a source of tension to the rest of the Population: adults with chronic (at least three
body leading to pain and to the loss of functional months) musculoskeletal pain excluding pain
capacity.2–5 It is believed that by stretching restricted associated with malignancy or specific neuro-
fascia, myofascial release therapy is able to normalize logical diseases like Parkinson disease, multiple
the length and the sliding properties of myofascial tis- sclerosis, and stroke.
sues releasing also pressure from the pain-sensitive Intervention: Myofascial release therapy exclud-
structures and restoring the mobility of the joints.2,3,6 ing myofascial trigger point treatment, non-
The descriptive characteristics and main results specific massage, or other types of manual
of previous narrative reviews on the effectiveness of therapy.
myofascial release therapy are presented in detail in
Supplementary Table 1. Even if these reviews Comparison: Any other treatment, placebo,
mostly reported encouraging evidence on the effec- sham, or no treatment
tiveness of myofascial release, none of the reviews Outcome: Between-group differences in changes
were sufficiently robust in terms of methodology in pain intensity or frequency, joint range of
and selection of studies to warrant a change in clini- motion, level of functioning, and quality of life.
cal practice. Five reviews included healthy partici- Differences between groups in satisfaction in
pants, one included mainly case studies, and the last treatment.
one reported results of two studies from only one
study group. No review has yet summarized the evi-
dence on the effectiveness of myofascial release in
Myofascial release therapy
chronic musculoskeletal pain patients based on ran- There are two main myofascial release tech-
domized controlled studies alone.4–10 niques in use: direct and indirect release. Both of
In previous reviews, there are no effect sizes to these techniques were included in this review.
support the reported encouraging conclusions on The direct release uses, for example, therapist’s
myofascial release. Based on the reviews of low- knuckles, elbows, or tools, and applies sustained
quality studies, the evidence of myofascial release few-kilogram pressure (90–120 seconds) directly
can at most be considered vague. When choosing on restricted tissue barriers. In turn, the indirect
appropriate treatment options in chronic pain, it release technique stretches myofascial complex
would be important to know whether the effect of by lower load and longer duration.2,4,6 Also, direct
Laimi et al. 3

myofascial release by patients themselves called reviewer groups rated methodological quality of
“self-myofascial release” was included. This included eight trials. Disagreements were resolved
kind of self-myofascial release uses various types by consensus or by a third reviewer (M.S.). Data
of roller massagers and provides tools for pain were extracted from included trials using a stand-
sufferers, athletes, and fitness trainers.5,7,8 In ath- ardized form based on recommendations by the
letes, self-myofascial release has thought to Cochrane Handbook for Systematic Reviews of
enhance range of joint motion, to speed up recov- Interventions Version 5.1.0. The methodological
ery, and to relieve prolonged muscle soreness5,7,8 quality was assessed according to the Cochrane
and has been suggested to be used as an alterna- Collaboration’s domain-based evaluation frame-
tive to massage. work (Supplementary Table 3). Main domains
Other manual therapies, different types of mas- were assessed in the following sequence: (1) selec-
sage, mobilization, or myofascial trigger point tion bias (randomized sequence generation and
therapy were not included in this review. Even if allocation concealment), (2) performance bias
the term “myofascial trigger point therapy” is (blinding of participants and personnel), (3) detec-
resembling “myofascial release,” trigger point tion bias (blinding of outcome assessment), (4)
therapy relies on a different theory and aims to the attrition bias (incomplete outcome data, e.g., due to
restoration of muscle function by treating muscular dropouts), (5) reporting bias (selective reporting),
“trigger points,” hyperirritable “knots” within taut and (6) other sources of bias. The scores for each
bands of skeletal muscles.4,11 bias domain and the final score of risk of system-
atic bias were graded as low, high, or unclear risk.12
The registration number of this review (Prospero
Search strategy database) is CRD42016035308.
The Cochrane Controlled Trials Register
(CENTRAL), Medline, Embase, CINAHL, PEDro,
and Scopus databases were searched for RCTs Minimal clinically important difference
(abstracts available in English) in February 2016 As clinically irrelevant statistically significant dif-
unrestricted by date, and the search was updated in ferences between intervention and control groups
August 2017. The search clauses are presented in are mainly dependent on the number of persons
Supplementary Table 2.12 We used the Cochrane examined, “minimal clinically important differ-
Highly Sensitive Search Strategy for identifying ence” is widely used to describe better the clinical
randomized trials. In order to avoid missing relevant relevance of findings. “Minimal clinically impor-
studies, use of limits was restricted and further selec- tant difference” is trying to define the smallest
tion was conducted manually. The references of the meaningful score change by separating “slightly
identified articles were also checked for relevancy. better result” from “almost equal” as the cut-off
point for minimal clinical importance for improve-
Study selection and methodological ment, independent of the sample size. This single-
point value is then generalized to other samples
quality assessment and is used on group level. Usually, this value is in
After saving all identified records in a citation the range of 6%–10% of the total score correspond-
manager (Endnote X7.2; Thomson Reuters, New ing to an effect size of 0.30–0.50 with different
York, NY, USA), clear duplicates, conference pro- estimates for different outcome instruments and
ceedings, theses, reviews, and expert opinions health conditions.13 Minimal clinically important
were deleted. Two independent reviewer groups difference has reported to be from 15% to 25% for
(E.B. and N.K. vs. A.M. and K.L.) screened all the numerical rating scale of neck pain, from 18% to
remaining 124 records based on titles and abstracts 28% for visual analogue scale of chronic low back
and, after that, based on the full texts of the selected patients, and even 38% to 51% for the functioning
potentially relevant studies. The same independent measurement in low back pain.14–20
4 Clinical Rehabilitation 00(0)

Quantitative analysis function reached minimal clinical importance in a


two-month follow-up,21,22 while the effect sizes of
A meta-analysis was inapplicable due to the dis- the two studies on fibromyalgia were either small
similarities of the included RCTs. The effect sizes or insignificant up to 12 months.26,27
of the main outcomes of the included studies were
calculated based on the reported mean values and
standard deviations at baseline and in follow-up. Discussion
The results were reported as raw mean differences In this first quantitative systematic review of RCTs
along with their standard errors and 95% confi- on the effectiveness of myofascial release therapy
dence intervals. All calculations for the quantita- in chronic musculoskeletal pain, the evidence was
tive analysis were performed using Comprehensive found to be scarce and inconsistent. The heteroge-
Meta Analysis (CMA, Version 3.3; Biostat, neity of study populations did not enable counting
Englewood Cliffs, NJ, USA) available from www. pooled effect sizes. When effect sizes of individual
meta-analysis.com. studies were counted, only three low-quality studies
reached clinically important short-term (up to two
months) improvement either in pain or functioning
Results when compared with sham treatment, while other
The search process is reported in Figure 1. Of 513 five studies did not show clinically significant dif-
records, finally 8 were considered relevant for quali- ferences between intervention and control groups.
tative analysis21–28 (Figure 1 and Supplementary One of the main weaknesses of our review was
Table 3). the fact that despite of systematic wide search, only
These eight relevant RCTs were involving in eight relevant studies were available for the analysis.
total 457 participants (Table 1). The duration of In addition, these studies came from only three
follow-up ranged from immediate assessment countries and five research groups. Five of the
after the end of treatment28 up to one year.27 The included studies were considered having high risk of
risk of bias was considered high in five of eight bias. Even if independent reviewers easily filtered
trials21–23,25,28 (Supplementary Table 3). Three myofascial release studies from other manual ther-
RCTs were conducted in the outpatient clinic of apy studies, and checking the reference lists of pre-
Myofascial Therapy and Research Foundation,21–23 vious reviews did not reveal caps in our study, it is
two samples involved the members of Fibromyalgia always possible that some relevant studies were
Association,26,27 one sample was gathered in a missed. To avoid this bias, all of reviewers were
physiotherapy outpatient department,28 and two in experienced physiotherapists or specialists of physi-
tertiary outpatient clinics.24,25 The control proce- cal and rehabilitation medicine. We also broadened
dures included sham myofascial release,23,24 sham our search from the original one in 2016 to the
ultrasound,21,22,27 or sham magnetotherapy.26 Two updated search in 2017, but widening search clauses
studies focused on adding myofascial release to added only one relevant article of “fascial manipula-
manual or physiotherapy25,28 (Table 1). tion.”25 Too narrow search clauses in systematic
Table 2 shows the main results of the included reviews would diminish the value of results espe-
studies along with the effect sizes. The authors of cially in the field of manual therapies with possibly
each of the eight studies concluded that myofascial many different terms for one type of therapy, while
release is effective in reducing pain and improving resembling names for different kinds of therapy. For
functioning. In a one- to three-month follow-up of example, “myofascial release” and “fascial manipu-
low back pain sufferers,23–25 reported changes did lation” are in the focus of our study, while “myofas-
not reach the minimal clinical importance except cial therapy” for muscular trigger points is not
for pain in one study with different baseline val- targeted to fascial tissues. As we only focused on
ues.25 In the studies on lateral epicondylitis and chronic pain patients, the results cannot be straightly
heel pain, the change in scales evaluating pain and extrapolated to acute musculoskeletal pain. The
Laimi et al. 5

Figure 1.  Flowchart of the search process.

scope of this review was narrowed down to the mobility of soft tissues remained unnoticed.
effects of myofascial release on pain relief, improved However, both clinical impression and the mobility
joint mobility, functioning, quality of life, and satis- of tissues, even if a target of myofascial release, are
faction after treatment. Thus, other relevant out- difficult to estimate objectively. If the main target of
comes, such as anxiety, clinical impression, or myofascial release is on restoring optimal length of
6

Table 1.  Descriptive characteristics of the included studies.


Study and Target population N (women %) Age (years), Follow-up Case treatment Control treatment Authors’ conclusion
country cases/controls
Cases Controls

Ajimsha et al.23 Nursing 38 (76) 36 (78) 36/34 Immediately Myofascial Sham myofascial Myofascial release as an adjunct to
and India professionals with (= 8 weeks) and release + back release + back back exercise is more effective than
low back pain 4 weeks after the exercises 3× 60 min/ exercises 3× exercise alone for chronic low back
end of treatment week, 8 weeks 60 min/week, pain in nursing professionals.
8 weeks
Ajimsha et al.22 Computer 33 (61) 32 (57) 31/29 Immediately Myofascial release 3× Sham ultrasound Myofascial release is more
and India professionals with (= 4 weeks) and 30 min/week, 4 weeks 3× 30 min/week, effective than sham ultrasound for
lateral epicondylitis 8 weeks after the 4 weeks lateral epicondylitis in computer
end of treatment professionals.
Ajimsha et al.21 Plantar heel pain 33 (76) 32 (69) 42/41 Immediately Myofascial release 3× Sham ultrasound Myofascial release is more effective
and India (= 4 weeks) and 30 min/week, 4 weeks 3× 30 min/week, than sham ultrasound in plantar heel
8 weeks after the 4 weeks pain.
end of treatment
Arguisuelas Non-specific low 27 (59) 27 (63) 47/46 Immediately Myofascial release 2× Sham myofascial Myofascial release produced a
et al.24 and Spain back pain (= 2 weeks), and 40 min/week, 2 weeks release 2× 40 min/ significant improvement in pain and
10 weeks after the week, 2 weeks disability.
end of treatment Minimal clinically important
differences were included in the 95%
CI. We cannot know whether this
improvement is clinically relevant.
Branchini et al.25 Non-specific low 11 (64) 13 (69) 48/44 Immediately Fascial manipulation Manual therapy Fascial manipulation led to decreased
and Italy back pain (= 4 weeks) and one 1× 45 min/ 2× 45 min/week, symptomatic, improved functional,
and three months week + manual 4 weeks and perceived well-being outcomes
after the end of therapy 1× 45 min/ that were greater amplitude
treatment week, 4 weeks compared to manual therapy alone.
Castro-Sánchez Fibromyalgia 30 (94) 29 (96) 49/46 Immediately Myofascial release of Sham Massage–myofascial release–therapy
et al.26 and Spain (20 weeks), 1 month tender points 90 min/ magnetotherapy reduces the sensitivity to pain at
and 6 months week, 20 weeks 30 min/week, tender points in fibromyalgia. Release
after the end of 20 weeks of fascial restrictions reduces anxiety
treatment and improves sleep quality, physical
function, and physical role. Massage–
myofascial release can be considered
as an alternative and complementary
therapy that can achieve transient
improvements.
Clinical Rehabilitation 00(0)
Laimi et al.

Table 1. (Continued)
Study and Target population N (women %) Age (years), Follow-up Case treatment Control treatment Authors’ conclusion
country cases/controls
Cases Controls

Castro-Sánchez Fibromyalgia 45 41 55/54 Immediately Myofascial release Sham short- Fibromyalgia patients can benefit
et al.27 and Spain Gender distribution not (20 weeks), 2× 60 min/week, wave + sham from myofascial release. Decrease
mentioned 6 months and 20 weeks ultrasound 2× in muscular tension secondary to
12 months after the 30 min/week, the release of myofascial restrictions
end of treatment 20 weeks improves physical function, fatigue,
number of days feeling good,
tiredness on walking, and stiffness.
Myofascial release significantly
improves several clinical dimensions,
with an important and consistent
improvement in pain, sensory, and
affective dimensions.
Khuman et al.28 Lateral 15 (40) 15 (47) 37/38 Immediately Myofascial Conventional Myofascial release improves pain,
and India epicondylitis (4 weeks) after the release + conventional physiotherapy 3×/ functional performance, and hand grip
end of treatment physiotherapy 3× week, 4 weeks for 4 weeks in lateral epicondylitis
30 min/week, 4 weeks probably by normalizing the fascial
tissue length and excitation of
afferent Aδ-fibers, which can cause
segmental pain modulation. Myofascial
release was more effective than
conventional physiotherapy alone for
pain, functional performance, and grip
strength.

CI, confidence interval.


7
8 Clinical Rehabilitation 00(0)

Table 2.  Effect sizes (raw mean difference in change between groups) of main outcomes of the included studies.
Study Outcome (scale) Reported results, mean (standard Mean Standard 95% Confidence
deviation) difference error interval

Cases Controls

Ajimsha et al.23 MPQ (0–78)


Baseline 23.2 (8.7) 23.0 (7.6)  
After treatment 10.8 (7.9) 17.0 (9.3) –6.4 1.76 –9.86 –2.94
4 weeks 13.1 (6.9) 18.3 (7.5) –5.4 1.62 –8.58 –2.22
QBPDS (0–100)
Baseline 37.1 (11.8) 35.3 (13.6)  
After treatment 26.9 (11.1) 31.8 (12.4) –6.7 2.55 –11.70 –1.70
4 weeks 28.7 (9.1) 32.5 (10.4) –5.6 2.42 –10.33 –0.87
Ajimsha et al.22 PRTEE (0–100)
Baseline 65.2 (5.9) 64.5 (4.9)  
After treatment 13.8 (2.2) 60.1 (5.7) –47.0 1.20 –49.36 –44.64
8 weeks 23.9 (4.1) 65.9 (4.5) –42.7 1.12 –44.89 –40.51
Ajimsha et al.21 FFI (0–100)
Baseline 63.0 (4.44) 61.4 (5.22)  
After treatment 17.4 (4.02) 56.9 (6.91) –41.1 1.17 –43.40 –38.80
8 weeks 24.8 (3.98) 60.2 (8.11) –37.0 1.30 –39.54 –34.46
Arguisuelas SF-MPQ (0–45)
et al.24 Baseline 22.3 (8.3) 23 (9.3)  
After treatment 13.08 (n/r)a 18 (n/r) –4.1 nr –10.2 –2.1
12 weeks 15.28 (n/r) 23.7 (n/r) –7.8 nr –14.5 –1.1
Pain (0–100)
Baseline 60.5 (23.9) 63.3 (24.0)  
After treatment 27.1 (n/r) 33.8 (n/r) –6.6 nr –20.9 –7.6
12 weeks 43.0 (n/r) 52.0 (n/r) –9.0 nr –25.8 –7.9
RMQ (0–24)
Baseline 59.7 (20.1) 63.6 (18.3)  
After treatment 7.5 (n/r) 10.1 (n/r) –2.6 nr –6.2 –1.0
12 weeks 8.1 (n/r) 11.8 (n/r) –3.7 nr –7.6 –0.2
FABQ (0–96)
Baseline 59.7 (20.1) 63.6 (18.3)  
After treatment 48.6 (n/r) 62.59 (n/r) –14.3 nr –27.8 –0.8
12 weeks 16.3 (n/r) 18.9 (n/r) –13.5 nr –27.6 –0.5
Branchini VAS (0–10)
et al.25 Baseline 5.5 (2.4) 2.6 (1.9)  
After treatment 0.4 (0.5) 1.1 (1.1) –3.6 0.7 –5.1 –2.1
1 month 0.6 (0.9) 2.2 (1.1) –4.5 0.7 –5.9 –3.1
3 months 1.1 (1.2) 2.0 (1.3) –3.8 0.7 –5.2 –2.4
SF-36 (0–100)
Baseline 58.0 (13.6) 57.7 (16.8)  
After treatment 85.9 (6.5) 67.5 (16.3) 18.1 5.4 7.5 28.7
1 month 83.7 (8.8) 69.6 (18.4) 13.8 5.7 2.7 24.9
3 months 82.4 (8.9) 70.3 (18.2) 11.8 5.6 0.8 22.8
BPI
Baseline 8.8 (3.9) 7.2 (2.5)  
After treatment 1.7 (1.3) 4.8 (3.2) –4.7 1.2 –7.1 –2.3
1 month 1.3 (1.8) 4.4 (3.2) –4.7 1.2 –7.0 –2.4
3 months 1.8 (1.9) 4.1 (3.6) –3.9 1.2 –6.3 –1.5
RMQ (0–24)
Baseline 6.9 (3.5) 7.0 (4.0)  
After treatment 1.8 (2.3) 3.9 (3.0) –2.0 1.3 –4.5 0.5
1 month 1.7 (2.1) 3.9 (3.1) –2.1 1.3 –4.6 0.4
3 months 1.5 (2.0) 4.1 (4.0) –2.5 1.3 –5.1 0.1

(Continued)
Laimi et al. 9

Table 2. (Continued)
Study Outcome (scale) Reported results, mean (standard Mean Standard 95% Confidence
deviation) difference error interval

Cases Controls

Castro- VAS (0–10)


Sánchez et al.26 Baseline 9.1 (1.1) 9.5 (1.3)  
After treatment 7.9 (1.8) 9.0 (1.3) –0.7 0.34 –1.37 –0.03
1 month 8.4 (1.1) 9.3 (1.1) –0.5 0.27 –1.03 0.03
6 months 8.8 (1.3) 9.7 (1.5) –0.5 0.31 –1.10 0.10
SF-36 (0–100)
Physical function  
Baseline 5.2b (5.4) 50.2 (8.5)  
6 months 48.2 (7.4) 51.2 (6.3) 4.8 1.68 1.50 8.10
Physical role
Baseline 26.0 (7.3 26.4 (6.3 1.6 1.67 –1.68 4.88
6 months 25.5 (8.4) 27.5 (6.3)  
Body pain
Baseline 76.6 (6.3) 78.9 (11.4)  
6 months 75.6 (8.2) 77.8 (9.7) 0.1 2.14 –4.10 4.30
General health
Baseline 67.8 (5.2) 68.8 (7.2)  
6 months 67.5 (7.2) 68.1 (6.4) 0.4 1.56 –2.65 3.45
Castro- FIQ (0–100)
Sánchez et al.27 Baseline 65.0 (18.2), 63.9 (16.4)  
6 months 58.6 (16.3) 64.1 (18.1) –6.6 3.35 –13.16 –0.04
12 months 62.8 (20.1) 65.0 (19.8) –3.3 3.64 –10.44 3.84
McGill Pain Scorea (0–45)
Baseline 25.0 (12.6) 25.3 (10.7)  
6 months 21.9 (7.2) 26.2 (6.8) –4.0 2.03 –7.98 –0.02
12 months 23.2 (7.6) 26.7 (6.9) –3.2 2.03 –7.17 0.77
VAS (0–10)
Baseline 9.1 (0.8) 8.9 (1.3)  
6 months 8.3 (1.1) 8.9 (1.3) –0.8 0.22 –1.24 –0.36
12 months 8.7 (1.1) 8.9 (1.0) –0.4 0.21 –0.81 0.01
Khuman et al.28 NRS (0–10)
Baseline 6.2 (1.65) 5.9 (1.38)  
After treatment 1.3 (0.48) 3.3 (1.23) –2.3 2.24 –6.69 2.09
PRTEE (0–100)
Baseline 57.8 (3.58) 59.7 (3.03)  
After treatment 10.1 (4.42) 31.3 (7.47) –19.3 1.85 –22.92 –15.68

MPQ, McGill Pain Questionnaire (0–78 points); QBPDS, Quebec Back Pain Disability Scale (0–100 points); PRTEE, patient-rated tennis elbow
evaluation (pain and functional disability; 0–100 points); FFI, Foot Function Index (0%–100%); SF-MPQ, Short Form McGill Pain Questionnaire (0–45
points); RMQ, Roland-Morris Questionnaire (0–24 points); FABQ, Fear Avoidance Beliefs Questionnaire (0–96 points); VAS, visual analogue scale for
pain intensity (0–10 cm), figures estimated from a graph; SF-36, 36-item Quality-of-Life Questionnaire (0–100 points); BPI, Brief Pain Inventory (two
subscales from 0 to 40 and 0 to 70 points, the used subscale not mentioned); FIQ, Fibromyalgia Impact Questionnaire (0–100 points); NRS, Numeri-
cal Rating Scale of pain intensity (0–10 points); nr, not reported.
aMcGill Pain Score Sensory and Affective (0–45 points).
bConsidered typo in the original article—value 5.2 replaced by 52.0 for the calculations.

fascia, this restoration is only a pathway in decreas- control treatment in a highly therapist-dependent
ing pain and enabling better functioning.2,4–6 manual treatment is important, as also touching can
Only three of the included RCTs23–25 had a credi- change the effectiveness of the treatment.9 As the
ble control group possibly capable in differentiating participants of the included studies were seeking for
the effect of myofascial release from the effect of a manual treatment option for their chronic pain,
manual touching. Blinding and choosing a credible non-manual sham control procedures—as in four
10 Clinical Rehabilitation 00(0)

included studies21,22,26,27—did probably not fulfill statistically significant improvement in functioning


their expectations. Six of eight studies were focusing reported by Ajimsha et al.16 (as measured by the
on intensive myofascial release treatment (12 to 24 Quebec Back Pain Disability Scale).
times in 4–20 weeks), and the follow-up times were In chronic musculoskeletal pain patients, the
mostly too short for the proper cost-effectiveness theoretical background of myofascial release pro-
evaluation.21–25,28 Despite these weaknesses, this vides one model when trying to explain functional
review was the first attempt to gather the evidence on changes of the body without measurable structural
effectiveness of myofascial release in chronic mus- diseases. As the application of myofascial release
culoskeletal pain systematically and to evaluate that relies on clinician–patient interaction, the subjectiv-
evidence both qualitatively and quantitatively. ity of the interaction cannot be removed when we
All previous narrative reviews on myofascial try to determine its outcome.9 Clinical treatment
release in other health conditions have concluded decisions rely on the scientific background, on cost-
with a suggestion that is favorable to release effectiveness, and on harmfulness of treatment
(Supplementary Table 1). Our quantitative review options. In future, high-quality RCTs conducted on
was unable to confirm these earlier positive conclu- larger samples with longer follow-ups may alter the
sions. One reason may lay in the differences between conclusion of this review.
target populations and in limiting study designs to
RCTs only. Due to these differences in the inclusion Clinical Messages
criteria, the earlier reviews are barely comparable
•• Current evidence of myofascial release
with our study. As regards the population of interest,
therapy in chronic pain relies on only a
the review closest to our review was probably one by
few studies.
McKenney et al.9 which evaluated myofascial
•• In quantitative analysis, previous posi-
release in orthopedic patients. However, as that tive conclusions could not be confirmed.
review included mainly case studies, the methodo- •• It is not known whether this kind of therapy
logical evaluation was not possible. The most impor- is more effective in treating chronic muscu-
tant difference between our study and previous loskeletal pain than sham procedures.
reviews may be hidden in including effect size calcu-
lations in this review. It is self-evident that small
positive effects seen in the majority of trials will Acknowledgements
inevitably lead to favorable conclusions of reviews if We want to thank University Hospital physiotherapists
minimal clinical importance of the results is Kirsi Peltonen and Sirpa Heinonen for their help during
ignored.13,14,16,19,20 Measuring effect size of interven- the evaluation of the included trials.
tion is vital in evaluating both statistical and clinical
significance of the results. For example, in a previous Declaration of conflicting interests
review by Yuan et al., myofascial release was The author(s) declared no potential conflicts of interest
reported to have large positive effects on fibromyal- with respect to the research, authorship, and/or publica-
gia based on two studies by Castro-Sánchez et al. tion of this article.
However, in these two studies, even if statistically
significant improvement in pain level was reported, Funding
the results did not even reach the clinical importance The author(s) received no financial support for the research,
as they fell under the level of 15%–28% (or 1.5 to 2 authorship, and/or publication of this article.
points on a numerical rating scale) that has been sug-
gested to represent a limit for minimal clinically References
important difference.15,18–20 Respectively, minimal
1. Park PW, Dryer RD, Hegeman-Dingle R, et al. Cost bur-
clinically important difference in measurement of den of chronic pain patients in a large integrated delivery
functioning in low back pain has previously been system in the United States. Pain Pract. Epub ahead of
proposed to be even 38%–51%, which is higher than print 7 October 2015. DOI: 10.1111/papr.12357.
Laimi et al. 11

2. Barnes MF. The basic science of myofascial release: mor- for pain and disability instruments in low back pain
phologic change in connective tissue. J Bodyw Mov Ther patients. BMC Musculoskelet Disord 2006; 7(1): 82.
1997; 1(4): 231–238. 17. Park KB, Shin JS, Lee J, et al. Minimum clinically impor-
3. Klingler W, Velders M, Hoppe K, et al. Clinical relevance tant difference and substantial clinical benefit in pain,
of fascial tissue and dysfunctions. Curr Pain Headache functional, and quality of life scales in failed back surgery
Rep 2014; 18(8): 439. syndrome patients. Spine 2017; 42(8): E474–E481.
4. Mauntel TC, Clark MA and Padua DA. Effectiveness 18. Pool JJM, Ostelo RWJG, Hoving JL, et al. Minimal clini-
of myofascial release therapies on physical performance cally important change of the neck disability index and the
measurements: a systematic review. Athl Train Sports numerical rating scale for patients with neck pain. Spine
Health Care 2014; 6(4): 189–196. 2007; 32(26): 3047–3051.
5. Schroeder AN and Best TM. Is self myofascial release an 19. Salaffi F, Stancati A, Silvestri CA, et al. Minimal clini-
effective preexercise and recovery strategy? A literature cally important changes in chronic musculoskeletal pain
review. Curr Sports Med Rep 2015; 14(3): 200–208. intensity measured on a numerical rating scale. Eur J Pain
6. Ajimsha MS, Al-Mudahka NR and Al-Madzhar JA. 2004; 8(4): 283–291.
Effectiveness of myofascial release: systematic review 20. Van der Roer N, Ostelo RW, Bekkering GE, et al.
of randomized controlled trials. J Bodyw Mov Ther 2015; Minimal clinically important change for pain intensity,
19(1): 102–112. functional status, and general health status in patients
7. Beardsley C and Skarabot J. Effects of self-myofascial with nonspecific low back pain. Spine 2006; 31(5):
release: a systematic review. J Bodyw Mov Ther 2015; 578–582.
19(4): 747–758. 21. Ajimsha MS, Binsu D and Chithra S. Effectiveness of myo-
8. Cheatham SW, Kolber MJ, Cain M, et al. The effects of fascial release in the management of plantar heel pain: a
self-myofascial release using a foam roll or roller mas- randomized controlled trial. Foot 2014; 24(2): 66–71.
sager on joint range of motion, muscle recovery, and 22. Ajimsha MS, Chithra S and Thulasyammal RP.
performance: a systematic review. Int J Sports Phys Ther Effectiveness of myofascial release in the management of
2015; 10(6): 827–838. lateral epicondylitis in computer professionals. Arch Phys
9. McKenney K, Elder AS, Elder C, et al. Myofascial release Med Rehabil 2012; 93(4): 604–609.
as a treatment for orthopaedic conditions: a systematic 23. Ajimsha MS, Daniel B and Chithra S. Effectiveness of
review. J Athl Train 2013; 48(4): 522–527. myofascial release in the management of chronic low back
10. Yuan SLK, Matsutani LA and Marques AP. Effectiveness pain in nursing professionals. J Bodyw Mov Ther 2014;
of different styles of massage therapy in fibromyalgia: 18(2): 273–281.
a systematic review and meta-analysis. Man Ther 2015; 24. Arguisuelas MD, Lison JF, Sanchez-Zuriaga D, et al. Effects
20(2): 257–264. of myofascial release in nonspecific chronic low back pain:
11. Lluch E, Nijs J, De Kooning M, et al. Prevalence, incidence, a randomized clinical trial. Spine 2017; 42(9): 627–634.
localization, and pathophysiology of myofascial trigger 25. Branchini M, Lopopolo F, Andreoli E, et al. Fascial
points in patients with spinal pain: a systematic literature manipulation® for chronic aspecific low back pain: a
review. J Manipulative Physiol Ther 2015; 38(8): 587–600. single blinded randomized controlled trial. F1000Res
12. Higgins J and Green S. Cochrane handbook for systematic 2015; 4: 1208.
reviews of interventions. The Cochrane Collaboration, 26. Castro-Sánchez AM, Mataran-Pearrocha GA, Granero-
http://handbook.cochrane.org/ (2011, accessed 4 August Molina J, et al. Benefits of massage-myofascial release
2016). therapy on pain, anxiety, quality of sleep, depression, and
13. Angst F. MCID: the minimal clinically important differ- quality of life in patients with fibromyalgia. Evidence-
ence assigns significance to outcome effects. J Rheumatol based complementary and alternative medicine, http://
2016; 43(2): 258–259. onlinelibrary.wiley.com/o/cochrane/clcentral/arti-
14. Hagg O, Fritzell P, Nordwall A, et al. The clinical cles/668/CN-00856668/frame.html
importance of changes in outcome scores after treat- 27. Castro-Sánchez AM, Mataran-Penarrocha GA, Arroyo-
ment for chronic low back pain. Eur Spine J 2003; Morales M, et al. Effects of myofascial release tech-
12(1): 12–20. niques on pain, physical function, and postural stability in
15. Kovacs FM, Abraira V, Royuela A, et al. Minimum detect- patients with fibromyalgia: a randomized controlled trial.
able and minimal clinically important changes for pain in Clin Rehabil 2011; 25(9): 800–813.
patients with nonspecific neck pain. BMC Musculoskelet 28. Khuman PR, Trivedi P, Devi S, et al. Myofascial
Disord 2008; 9: 43. release technique in chronic lateral epicondylitis: a ran-
16. Lauridsen HH, Hartvigsen J, Manniche C, et al. Respon- domized controlled study. Int J Health Sci Res 2013;
siveness and minimal clinically important difference 3(7): 45–52.

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