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Neural mobilization in low back and radicular pain: a systematic review Mica Peacock*, Samuel Douglas* and Preeti Nair Samuel Merritt University, Department of Physical Therapy, Oakland, CA, USA ABSTRACT Background: Low back pain can present with radicular pain caused by lumbosacral nerve root pathology. Neural mobilization (NM) is a treatment technique used to treat low back and radicular pain (LBRP). Purpose: To evaluate the effectiveness of NM interventions in improving pain, disability, and function in adults with LBRP. Data Sources: CINAHL Plus, MEDLINE (Ovid), Physiotherapy Evidence Database, and Cochrane databases were searched. Study Selection: Randomized controlled trials assessing the effect of NM on pain, disability, and/or function in adults with LBRP. Data Extraction: Authors reviewed studies and used the PEDro scale and the revised Cochrane risk-of-bias tool to assess methodological quality and risk of bias. Data Synthesis: Eight studies were included. Six of the eight studies found the addition of NM to conservative treatment improved all measured outcomes. One study found improvements in some but not all functional measures, and delayed improvements in pain. One study found improvements in measures of neural sensitivity, but not overall pain and disability. Conclusions: NM may be an effective tool for short-term improvements in pain, function, and disability associated with LBRP. Additional high quality research is needed. Study registration: : This systematic review protocol was registered with PROSPERO (registra- tion number: CRD42020192338). KEYWORDS Neural mobilization; nerve root; low back pain; sciatica; radicular Introduction Low Back and Radicular Pain (LBRP), defined as pain due to compression, irritation, or other pathology of one or more lumbosacral nerve roots, is one of the most common forms of low back pain [1–3]. Annual prevalence has been reported as high as 25% and lifetime prevalence as high as 43% [1,4]. Not only is LBRP common it is significantly debilitating. Compared to other forms of low back pain, LBRP is associated with a variety of poor outcomes. These outcomes include more severe and persistent pain, increased cost of care, and longer periods of disability and absence from work [1,5–7]. Therefore there is a need to treat this promptly and effectively. In terms of isolating the cause of pain, lumbar disc herniation is widely considered the most common cause of LBRP [8–10]. However, LBRP may also be caused by osteophytes, spondylolisthesis, and other local factors. Symptom presentation of LBRP usually involves pain characterized as sharp, burning, dull, aching or lancinating that radiates from the lower back below the gluteal fold and follows a dermatomal distribution based on the level of spinal root pathology[11]. In addition to pain, other symptoms may also exist and include paresthesia, weakness, and diminished ankle and/or knee reflexes [9]. No single assessment serves as the gold standard for diagnosis of LBRP, so a medical diagnosis of LBRP is therefore only reached after a combination of imaging studies, a detailed review of the patient’s symptoms, and the performance of a physical examination[9]. Given the variety of causative factors involved, range of symptom presentation, and difficulty in reaching an accurate diagnosis, LBRP is a challenging condition to diagnose and treat. Treatment options for LBRP include conservative care, pharmaceutical interventions and surgery. Conservative care options are varied and may include a variety of exercise protocols, electrical modalities such as transcutaneous electrical nerve stimulation, and techniques aimed at mobilizing the affected tissue such as spinal mobilization, and neural mobilization (NM)[12]. Neural mobilization refers to the therapeutic prac- tice of applying mechanical forces to nerves in the body, with the goal of restoring healthy movement. Nerves must be able to move within the nerve bed (i.e. surrounding tissue) for normal movement to occur, CONTACT Mica Peacock mica.peacock@samuelmerritt.edu Samuel Merritt University, Department of Physical Therapy, 3100 Telegraph Avenue Oakland, Oakland, CA 94609, USA The authors report no conflict of interest. *Both authors contributed equally to this work and are co-first authors Supplemental data for this article can be accessed here. JOURNAL OF MANUAL & MANIPULATIVE THERAPY 2023, VOL. 31, NO. 1, 4–12 https://doi.org/10.1080/10669817.2022.2065599 © 2022 Informa UK Limited, trading as Taylor & Francis Group http://orcid.org/0000-0002-1609-0050 https://doi.org/10.1080/10669817.2022.2065599 http://www.tandfonline.com https://crossmark.crossref.org/dialog/?doi=10.1080/10669817.2022.2065599&domain=pdf&date_stamp=2023-01-11 and tolerate strain, compression, and transverse move- ment along the nerve bed[13]. Some NM techniques directly mobilize the neural tissue (e.g. nerve glide, nerve flossing) via either active (e.g. exercise) or pas- sive (e.g. manual therapy) techniques[14]. Others indir- ectly mobilize the nerves via movement of the surrounding tissues (e.g. spinal mobilization)[15]. NM may be helpful for decreasing pain and restoring nerve function in a variety of musculos- keletal conditions, but its effects on LBRP are not well-studied[16–21]. A 2014 critical review by Efstathiou et al [22] concluded that the existing literature was too sparse and low-quality in deter- mining the effectiveness of treating lumbar radi- culopathy with NM. More recently, a 2016 systematic review by Su and Lim [23] found that NM interventions provided pain relief and reduc- tion in disability for people with nerve-related chronic musculoskeletal disorders, but found no significant differences between NM and other con- servative treatments. Finally, a 2017 systematic review by Basson et al [14] on the efficacy of treating various musculoskeletal conditions with NM found that a variety of NM techniques can improve pain and disability in these participants. Given the lack of consensus on the functional effects of NM on LBRP, this field of research would benefit from a systematic review focused solely on a population with lumbar radicular pain. The objec- tive of this systematic review was to evaluate the effectiveness of NM interventions in improving pain, disability, and function in adults with LBRP. Methods Study registration Study registration: This systematic review protocol was registered with PROSPERO (registration number: CRD42020192338), and was performed in line with the PRISMA declaration guidelines. Search strategy The databases searched in this systematic review were CINAHL Plus, MEDLINE (Ovid), Physiotherapy Evidence Database, and Cochrane Central Register of Controlled Trials. All searches were performed in May 2020. Our search strategy targeted clinical trials with two primary variables of interest, a specific participant population (people with LBRP) and our specific intervention (neural mobilizations). Our search strategy included terms related to LBRP, including sciatica, neurogenic, and disc herniation, as well as related terms for neural mobilization interventions, including nerve modality, nerve ten- sion, and nerve flossing. For CINAHL Plus, we also limited our searches to randomized controlled trials (RCTs) and excluded MEDLINE records. No filters related to publication date were used for any of our searches, and no limitations on outcome mea- surement timeline were applied prospectively. See Appendix 1 for an example search strategy. Eligibility criteria RCTs, available in English, assessing the effect of NM on pain, function, or disability in adults with LBRP were eligible for inclusion. Included studies met the following criteria: (1) Participant populations presented with symptoms, radiological findings, or other clinical findings of LBRP. These included radiological findings of lumbar disc herniation or degeneration,back pain radiating down into at least one lower extremity, reproduc- tion of symptoms with passive straight leg raise (PSLR) or slump test, myotomal weakness, dermato- mal change in sensation, or hyporeflexia in a lumbosacral innervation pattern. (2) NM interven- tion was provided using methods that directly mobilize the neural tissue (e.g. nerve glide, nerve flossing) via either active (e.g. exercise) or passive (e.g. manual therapy) techniques. Eligible compara- tor/control conditions included no treatment, sham treatment, or conservative treatment not involving neural mobilization. (3) Outcomes assessed at least one of our primary outcomes of interest (pain, dis- ability, and function), via scales such as the Numeric Pain Rating Scale (NPRS), Visual Analog Scale (VAS), Oswestry Disability Index (ODI), Roland-Morris Disability Questionnaire (RMDQ), or the Short Form Health Survey (SF-36 or SF-12). Animal studies, case reports, cohort studies, and studies on healthy participants were excluded. Studies with patient populations including evidence or indication of specific spinal pathology (including but not limited to vertebral fracture, neoplasm, cauda equina syndrome, and spinal infection), systemic neu- rological disorders or lesions, or low back pain without radicular qualities were also excluded. Studies compar- ing two separate interventions with no control condi- tion were excluded, as were studies assessing NM only performed by indirect mobilization of the nerves via movement of the surrounding tissues (e.g. spinal mobilization). Two reviewers (SD and MP) independently screened titles and abstracts of records identified via the described search strategy using these inclu- sion and exclusion criteria. Full-text of appropriate studies were screened independently for inclusion by both reviewers. Discrepancies were resolved by consensus meeting. In the case of continued dis- agreement, a third reviewer would have been used to determine eligibility for inclusion. JOURNAL OF MANUAL & MANIPULATIVE THERAPY 5 Data extraction and quality assessment Data were systematically extracted from the abstract and full-text of each study. The following items were included: author name and year of pub- lication, participant demographics, experimental and control treatment protocols, all outcome para- meters including assessment timing, and main results. Articles that met the inclusion criteria were assessed using the PEDro scale and the revised Cochrane risk-of- bias tool (RoB2). The PEDro scale is a valid and reliable tool for measuring the methodological quality of clinical trials[24]. The scale provides a rating for each study between zero and ten based on a series of “yes or ‘no’ questions, with a score of >8 considered excellent, a score of 6 to 8 considered good, a score of 4 to 5 considered fair, and a score of 35 degrees[27], while two papers [32,33] excluded participants with a positive PSLR of 14 female, 16 male n = 15 35.1 (6.4) years – n = 15 41.6 (11.1) years – Nagrale et al. 2013 n = 60: 39 female, 21 male n = 30 38.2 (3.47) years 66.31 (11.16) weeks n = 30 37.76 (4.70) years 64.14 (7.78) weeks Pallipamula & Singaravelan 2012 n = 42 n = 21 42.53 (6.99) years 9.09 (1.89) weeks n = 21 40.2 (7.55) years 8.91 (1.80) weeks Plaza-Manzano et al. 2020 n = 32: 16 female, 16 male n = 16 45.4 (6.0) years 75.2 (6.1) weeks n = 16 47.0 (8.0) years 74.7 (6.5) weeks Satishkumar et al. 2017 n = 38 n = 19 34.11 (8.36) years 32.02 (12.38) weeks n = 19 35.47 (8.40) years 31.55 (11.12) weeks SD: standard deviation JOURNAL OF MANUAL & MANIPULATIVE THERAPY 7 Ta bl e 2. In te rv en tio n Pr ot oc ol s, O ut co m e M ea su re s, a nd R es ul ts o f I nc lu de d St ud ie s. Pr ot oc ol O ut co m e M ea su re s Re su lts St ud y N er ve M ob ili za tio n Tr ea tm en t Co nt ro l G ro up T re at m en t Fr eq ue nc y, D ur at io n, Se ss io ns O M s us ed (* d en ot es tr an sl at ed v er si on ) O M t im in g (* de no te s tr an sl at ed ve rs io n) Si gn ifi ca nt fi nd in gs N on -s ig ni fic an t fin di ng s Ah m ed e t al . 20 13 pa ss iv e ne ur od yn am ic s lid er in s up in e PS LR po si tio n w ith b ia s to p er on ea l o r tib ia l ne rv es ; H EP w ith n er ve fl os si ng t ec hn iq ue fle xi on o r ex te ns io n ex er ci se s, 30 m in p er d ay , 1 0 re ps , 2 –3 s et s of 1 0 re ps p er e xe rc is e; T EN S – al on g sc ia tic n er ve t ra ct , 1 00 H z fo r 30 m in ut es p er s es si on 3x /w k; 2 w ks ; 6 in -p er so n tr ea tm en ts N PR S; S F- 12 at b as el in e af te r w k 3* IG t re at m en t fa vo re d fo r bo th ou tc om es Cl el an d et a l. 20 06 st at ic s lu m p st re tc h w ith o ve rp re ss ur e in lo ng si tt in g; D ai ly H EP w ith s am e te ch ni qu e 5- m in e xe rc is e bi ke ; g ra de II I– IV lu m ba r sp in e m ob ili za tio ns ; st an da rd iz ed e xe rc is e pr og ra m ta rg et in g lo w b ac k pa in ; H EP o f st an da rd iz ed e xe rc is e pr og ra m 2x /w k; 3 w ks ; 6 in -p er so n tr ea tm en ts 1 8 H EP s es si on s O D I; N PR S; L oc at io n of sy m pt om s (b od y ch ar t) at b as el in e af te r w k 3* IG t re at m en t fa vo re d fo r al l ou tc om es Fe rr ei ra e t al . 20 16 gr ad e III lu m ba r fo ra m en o pe ni ng m ob ili za tio ns ; p as si ve n eu ro dy na m ic s lid er in s id el yi ng ; p ro gr es se d to a ct iv e ne ur od yn am ic s lid er in s lu m p si tt in g; D ai ly H EP w ith s lid in g an d te ns io ni ng t ec hn iq ue s ad vi ce t o re m ai n ac tiv e 2x /w k; 2 w ks ; 4 in -p er so n tr ea tm en ts 1 4 H EP s es si on s N PR S (le g an d lo w ba ck ); O D I 2 .0 *; PS FS ; L oc at io n of sy m pt om s (b od y ch ar t) ; G PE at b as el in e af te r w k 2* af te r w k 4 IG t re at m en t fa vo re d fo r PS FS an d G PE a ft er 2 w ee ks ; I G tr ea tm en t fa vo re d fo r le g N PR S, lo w b ac k N PR S, P SF S, an d G PE a ft er 4 w ee ks N o si gn ifi ca nt B G d iff er en ce s fo r O D I 2. 0 an d lo ca tio n of s ym pt om s at an y tim ep oi nt s; N o si gn ifi ca nt B G di ffe re nc es fo r le g or lo w b ac k N PR S af te r 2 w ee ks Je on g et a l. 20 16 ac tiv e ne ur od yn am ic t en si on er in s ea te d po si tio n lu m ba r se gm en ta l s ta bi liz at io n ex er ci se p ro gr am t ar ge tin g tr an sv er su s ab do m in is a nd m ul tifi du s 3x /w k; 6 w ks ; 1 8 tr ea tm en ts SF -3 6 PF a nd G H su bs co re s at b as el in e af te r w k 6* IG t re at m en t fa vo re d fo r bo th ou tc om es N ag ra le e t al . 20 13 st at ic s lu m p st re tc h w ith o ve rp re ss ur e in lo ng si tt in g; D ai ly H EP w ith s am e te ch ni qu e 5- m in e xe rc is e bi ke ; g ra de II I– IV lu m ba r sp in e m ob ili za tio ns ; st an da rd iz ed e xe rc is e pr og ra m ta rg et in g lo w b ac k pa in 2x /w k; 3 w ks ; 6 in -p er so n tr ea tm en ts 1 8 H EP s es si on s N PR S; O D I; FA BQ at b as el in e af te r w k 1 af te r w k 2 af te r w k 3* af te r w k 6 IG t re at m en t fa vo re d fo r N PR S an d FA BQ a ft er w ee ks 1 a nd 2; IG t re at m en t fa vo re d fo r al l o ut co m es a ft er w ee ks 3 an d 6 N o si gn ifi ca nt B G d iff er en ce fo r O D I af te r w ee ks 1 a nd 2 Pa lli pa m ul a & Si ng ar av el an 20 12 ac tiv e ne ur od yn am ic s lid er in s ea te d sl um p po si tio n TE N S al on g th e ar ea o f s ym pt om s; m ec ha ni ca l l um ba r tr ac tio n 1x d ai ly ; 6 d ay s; 6 se ss io ns o f N M a nd T EN S 3 se ss io ns o f lu m ba r tr ac tio n VA S; S ci at ic a Bo th er so m en es s Sc al e; P SL R; A ct iv e Lu m ba r Fl ex io n; M od ifi ed O D I at b as el in e af te r 6 da ys * IG t re at m en t fa vo re d fo r al l ou tc om es Pl az a- M an za no et a l. 20 20 pa ss iv e ne ur od yn am ic s lid er in s up in e ta rg et in g sc ia tic n er ve m ot or c on tr ol e xe rc is e pr og ra m ta rg et in g tr an sv er su s ab do m in is an d m ul tifi du s; H EP w ith s am e ex er ci se s 2x /w k; 4 w ks ; 8 tr ea tm en ts N PR S; S -L AN SS ; R M D Q ; PS LR ; P PT at b as el in e af te r 2 w ks af te r 4 w ks * 2 m on th s af te r fin al se ss io n IG t re at m en t fa vo re d fo r S- LA N SS a nd S LR N o si gn ifi ca nt g ro up *t im e in te ra ct io ns fo r N PR S, R M D Q , a nd PP T Sa tis hk um ar et a l. 20 17 ac tiv e ne ur od yn am ic s lid er in s ea te d sl um p po si tio n lu m ba r st ab ili za tio n ex er ci se s, pr og re ss ed w ee kl y 5x /w k; 4 w ks ; 2 0 tr ea tm en ts N PR S; R M D Q *; P SL R; FA BQ * at b as el in e af te r w k 1 af te r w k 2 af te r w k 4* IG t re at m en t fa vo re d fo r al l ou tc om es a ft er w ee ks 1 , 2 an d 4 N PR S: N um er ic P ai n Ra tin g Sc al e; S ho rt F or m H ea lth S ur ve y (S F- 36 o r SF -1 2) ; P F: p hy si ca l f un ct io ni ng ; G H : g en er al h ea lth ; O D I: O sw es tr y D is ab ili ty In de x; P SF S: P at ie nt S pe ci fic F un ct io na l S ca le ; G PE : G lo ba l P er ce iv ed E ffe ct ; F AB Q : F ea r Av oi da nc e Be lie fs Q ue st io nn ai re ; V AS : V is ua l A na lo g Sc al e; P SL R: p as si ve s tr ai gh t le g ra is e; S -L AN SS : L ee ds A ss es sm en t of N eu ro pa th ic S ym pt om s an d Si gn s (s el f- re po rt v er si on ); RM D Q : R ol an d- M or ris D is ab ili ty Q ue st io nn ai re ; T EN S: tr an sc ut an eo us e le ct ric al n er ve s tim ulat io n; S M D : s ta nd ar di ze d m ea n sc or e di ffe re nc e; M D : m ea n di ffe re nc e; B G : b et w ee n gr ou ps ; I G : i nt er ve nt io n gr ou p; C G : c on tr ol g ro up ; C I: co nfi de nc e in te rn al ; H EP : h om e ex er ci se p ro gr am ; P PT : pr es su re p ai n th re sh ol d 8 M. PEACOCK ET AL. Ta bl e 3. P ED ro a nd C oc hr an e Q ua lit y As se ss m en t. PE D ro Co ch ra ne 1 2 3 4 5 6 7 8 9 10 11 to ta l s co re * Su bs co re s D om ai ns 1 –5 O ve ra ll Ri sk Ah m ed e t al . 2 01 3 y y y y n n n n n y y 5/ 10 1: lo w r is k 2: h ig h ris k 3: s om e co nc er ns 4 : h ig h ris k 5: s om e co nc er ns hi gh r is k Cl el an d et a l. 20 06 y y y y n n y y y y y 8/ 10 1: lo w r is k 2: lo w r is k 3: lo w r is k 4: lo w r is k 5: s om e co nc er ns so m e co nc er ns Fe rr ei ra e t al . 2 01 6 y y y y n n y y y y y 8/ 10 1: lo w r is k 2: lo w r is k 3: s om e co nc er ns 4 : l ow r is k 5: lo w r is k so m e co nc er ns Je on g et a l. 20 16 y y n n n n n n n y y 3/ 10 1: s om e co nc er ns 2 : h ig h ris k 3: s om e ris k 4: lo w r is k 5: h ig h ris k hi gh r is k N ag ra le e t al . 2 01 3 y y y y n n y y y y y 8/ 10 1: lo w r is k 2: lo w r is k 3: lo w r is k 4: lo w r is k 5: s om e co nc er ns so m e co nc er ns Pa lli pa m ul a & S in ga ra ve la n 20 12 y y n y n n n y n y y 5/ 10 1: s om e co nc er ns 2 : l ow r is k 3: s om e co nc er ns 4 : h ig h ris k 5: s om e co nc er ns hi gh r is k Pl az a- M an za no e t al . 2 02 0 y y y y n n y y y y y 8/ 10 1: lo w r is k 2: lo w r is k 3: lo w r is k 4: lo w r is k 5: s om e co nc er ns so m e co nc er ns Sa tis hk um ar e t al . 2 01 7 y y y y n n n n n y y 5/ 10 1: lo w r is k 2: h ig h ris k 3: s om e ris k 4: h ig h ris k 5: s om e co nc er ns hi gh r is k *c rit er io n 1 no t in cl ud ed JOURNAL OF MANUAL & MANIPULATIVE THERAPY 9 quality assessments, with the fair and poor quality papers judged to be high risk, and the four good quality studies judged to have some concerns. Quality assessment scores for all studies are available in Table 3. No trials were able to blind the therapist to the intervention they were delivering. This reflects an ongoing challenge in the field rather than a failing of these studies in particular. Several studies that per- formed physical assessments as outcome measures did not specify whether the assessor was blinded to the intervention group. Only one paper [28] pre- published their study design in order to allow assess- ment of result reporting bias. Results Table 2 describes the results of each individual study included in this systematic review. All eight included studies measured disability or function as a primary outcome. Four [28,29,32,33] used the standard, mod- ified, or revised version of the ODI, two [30,31] used the RMDQ, and one study each used the Patient Specific Functional Scale (PSFS)[28], SF-12[27], and select sub- scales of the SF-36[34]. Seven of the studies included pain as a primary outcome measure, with six [27,28,30– 33] using the 11-point NPRS. Only three studies [28,30,33] re-assessed outcomes at a follow-up later than the final treatment session, and only one [30] assessed any outcomes later than six weeks following initial treatment. Disability/Function Five of the eight included studies found significant between-group differences favoring NM treatment for all outcomes related to function or disability at all post- baseline measurements [27,29,31,32,34]. Of the remain- ing three studies, Nagrale et al [33] found significant between-group differences favoring NM treatment for the ODI after weeks 3 and 6. Ferreira et al [28] had mixed results, with the PSFS showing significant between-group differences favoring NM treatment after week 2 and week 4, but no significant differences for the ODI. Plaza-Manzano et al [30] found no signifi- cant group*time interaction for the RMDQ. Pain Of the seven studies that included at least one mea- sure of pain, five found significant between-group dif- ferences favoring NM treatment for all outcomes related to function or disability at all post-baseline measurements [27,29,31–33]. Of the remaining two studies, Ferreira et al [28] found significant between- group differences favoring NM treatment after week 4 in leg and low back NPRS scores. Plaza-Manzano et al [30] found significant group*time interactions for the PSLR and the Leeds Assessment of Neuropathic Symptoms and Signs (a measure of neuropathic pain), but not for the NPRS or pressure pain threshold. Discussion The goal of this systematic review was to determine the effectiveness of NM in treating adults with LBRP. This subset of low back pain patients experiences worse outcomes on average[1], but has been inconsis- tently defined pathologically in prior research, limiting the ability to draw conclusions about effective treat- ments. NM was chosen as the intervention of interest because it has been shown to be effective in treating nerve-related pain in other body regions[14], but evi- dence related to lumbosacral pain is limited. Six of the eight RCTs included in this review found that adding an NM intervention to a conservative treat- ment plan improved all outcomes. The results of the remaining two papers favored NM treatment for some outcomes; Plaza-Manzano et al [30] found improve- ments in measures of neural sensitivity, but not overall pain and disability, while Ferreira et al [28] found improvements in some but not all functional measures, and delayed improvements in pain. Furthermore, no studies found any evidence of NM treatment having a detrimental effect on any outcomes. Overall, the collective results of these eight studies indicate that NM may be recommended for treatment of LBRP, although data are still too limited to determine the extent to which NM contributes to the effectiveness of a multi-modal treatment plan. The low quality and inconsistent rigor of the included studies is a limitation of this review. Only four of the eight included studies achieved a quality rating of good on the PEDro scale and a RoB2 risk assessment lower than ‘high.’ Several studies failed to include critical information such as the proportion of randomized participants who completed the entire study, and the details of the concealed allocation pro- cess used for randomization. Ahmed et al [27] stated that participants were given a home exercise program but gave no information about the frequency with which they performed it. Jeong et al [34] described the steps of the NM technique performed, but gave no indication of whether the technique was performed for multiple repetitions within a treatment session, and provided no rationale for their choice of the general health and physical functioning subscales of the SF-36 as sole outcome measures. The substantial variability in intervention design, frequency, and duration, as well as symptom intensity and duration in participant populations, limits our abil- ity to draw conclusions about the efficacy of the use of any specific NM protocol. Our conclusions regarding long-term effects are also limited because only three 10 M. PEACOCK ET AL. studies re-assessed outcomes after the final treatment session. The breadth of positive findings when NM is added to a wide variety of control interventions does confirm that NM can be an appropriate part of a multi- modal treatment plan for people with LBRP. The lack of consensus regardinglanguage to describe LBRP limits the ability of researchers and clin- icians to understand and discuss this unique population. The term ‘sciatica,’ while easily recognized, is not anato- mically descriptive. Its continued use to describe both nerve root pathology and peripheral nerve involvement conflates two very different clinical presentations. The use of the term ‘radicular’ is also inconsistent across studies. The word’s literal meaning is ‘pertaining to the nerve root,’ but it has been conflated with ‘radiculopa- thy’ and therefore assumed to only apply to severe nerve root compromise. For example, Cleland et al [32] and Nagrale et al [33] go so far as to claim that their study populations have ‘non-radicular low back pain’ by nature of excluding participants who have diminished reflexes, sensation, or strength, despite all participants exhibiting low back pain that radiates below the gluteal fold and is reproduced with slump testing. This level of inconsistency in the use of the word radicular has the potential to actively create confusion. Additional high quality RCTs on this subject are necessary to further explore the treatment of LBRP with NM. It is especially important that future RCTs on this topic use precise and consistent criteria to define the participant population. We recommend future studies use a predetermined duration of symp- toms, a standardized method of identifying radicular symptoms, and longer follow-up periods. Standardized intervention protocols would also significantly reduce the overall study heterogeneity and improve the extent to which these findings can be generalized. In conclusion, our findings suggest that NM may be an effective tool for short-term improvements in pain, function, and disability associated with LBRP. Robust claims regarding the utility of particular intervention protocols will require publication of additional high- quality RCTs with detailed, homogenous study protocols. Notes on Contributors Mica Peacock earned her Bachelor of Arts in Biology from Reed College, and received her Doctor of Physical Therapy degree at Samuel Merritt University. Samuel Douglas received his Bachelor of Arts in Neuroscience and Behavior from Wesleyan University, and received his Doctor of Physical Therapy degree at Samuel Merritt University. Preeti Nair earned her Bachelor of Physiotherapy at Pune University in India. She then earned a PhD in Rehabilitation Sciences at the University of Florida, with a research focus on Biomechanics and Neurophysiology of walking in individuals with neurological impairment. She is currently an Associate Professor in the Department of Physical Therapy at Samuel Merritt University. Disclosure statement Authors report no conflict of interest. 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Effect of slump stretching versus lumbar mobilization with exercise in subjects with non-radicular low back pain: a randomized clinical trial. J Man Manip Ther. 2012;20 (1):35–42. [34] Jeong UC, Kim CY, Park YH, et al. The effects of self- mobilization techniques for the sciatic nerves on phy- sical functions and health of low back pain patients with lower limb radiating pain. J Phys Therapy Sci. 2016;28(1):46–50. 12 M. PEACOCK ET AL. https://doi.org/10.1016/s1836-9553(12)70069-3 https://doi.org/10.1016/s1836-9553(12)70069-3 https://doi.org/10.1097/PHM.0000000000001295 https://doi.org/10.1097/PHM.0000000000001295 Abstract Introduction Methods Study registration Search strategy Eligibility criteria Data extraction and quality assessment Data synthesis and analysis Study selection Study characteristics Methodological quality Results Disability/Function Pain Discussion Notes on Contributors Disclosure statement ORCID References