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. 2022 Dec 6;17(12):e0278177. doi: 10.1371/journal.pone.0278177

Comparison of neural mobilization and conservative treatment on pain, range of motion, and disability in cervical radiculopathy: A randomized controlled trial

Shazia Rafiq 1,*, Hamayun Zafar 2,3,4,5, Syed Amir Gillani 6, Muhammad Sharif Waqas 7, Amna Zia 8, Sidrah Liaqat 8, Yasir Rafiq 9
Editor: Walid Kamal Abdelbasset10
PMCID: PMC9725158  PMID: 36472990

Abstract

Objective

The objective of the study was to compare the effectiveness of neural mobilization technique with conservative treatment on pain intensity, cervical range of motion, and disability.

Methods

It was a randomized clinical trial; data was collected from Mayo Hospital, Lahore. Eighty-eight patients fulfilling the sample selection criteria were randomly assigned into group 1 (neural mobilization) and group 2 (conventional treatment). Pain intensity was measured on a numeric pain rating scale, range of motion with an inclinometer, and functional status with neck disability index (NDI). Data were analyzed using SPSS, repeated measure ANOVA for cervical ranges and the Friedman test for NPRS and NDI were used for within-group analysis. Independent samples t-test for cervical ranges and Mann-Whitney U test for NPRS and NDI were used for between-group comparisons.

Results

There was a significant improvement in pain, disability, and cervical range of motion after the treatment in both groups compared to the pre-treatment status (p < 0.001), and when both groups were compared neural mobilization was more effective than conventional treatment in reducing pain and neck disability (p < 0.001), but there was no significant difference present in the mean score of cervical range of motion between both groups. (p>0.05).

Conclusions

The present study concluded that both neural mobilization and conservative treatment were effective as an exercise program for patients with cervical radiculopathy, however, neural mobilization was more effective in reducing pain and neck disability in cervical radiculopathy.

Trial registration

RCT20190325043109N1.

Introduction

Cervical Radiculopathy (CR) is a disorder of the spinal nerve roots that are largely caused by a space-occupying lesion, disc herniation compression, and bony spur typically osteophytes in degenerating cervical spine which can lead to nerve root inflammation, impingement, or both [1]. These lesions can trigger pain receptors in the soft tissues and joints of the cervical spine that can lead to both sensory or motor changes in the upper extremity such as loss of or altered sensation, numbness and tingling in the upper extremity, muscular weakness in the arms, hands, neck or scapular region, and pain along the nerve pathways into the hand and arm, depending on affected nerve roots [2, 3]. The incidence of cervical radiculopathy annually is about 107.3 per 100,000 for males and 63.5 per 100, 000 for females. This incidence increases in the fifth decade of life up to 203 per 100 000 [4].

Among the Pakistani population, irregular physical activity, intensifying stress levels and deficiency of exercise are causing tremendous problems in daily routine [5]. These factors result in the bone, immune system, and muscle weakness as well as disturbance of normal body mechanics, resulting in instability of the spinal segments and related structures that aggravate the underlying musculoskeletal problems [6]. For establishing criteria for the diagnosis of cervical radiculopathy, different diagnostic tests are devised. MRI and EMG are important for diagnosing cervical radiculopathy [7].

Cervical radiculopathy can be treated surgically but there is a large number of evidence suggesting conservative management to be more effective than surgical treatment, suggesting multimodal treatment strategies that include cervical traction, manual therapy techniques, and strengthening exercises [8, 9].

Although there are limited high-quality evidences on the best nonoperative therapy for cervical radiculopathy, these are used to relieve discomfort and pain [8, 10, 11]. Neural mobilizations have been studied in various populations such as low back pain, carpal tunnel syndrome, lateral epicondylalgia, and cervicobrachial pain [12]. Neural mobilization is said to affect the axoplasmic flow, movement of the nerve and its connective tissue and the circulation of the nerve by alteration of the pressure in the nervous system and dispersion of intraneural edema. Nerve gliding exercises are a sequence of the positioning of the upper limb or lower limb to elongate nerves used in the treatment of multiple musculoskeletal disorders. However further research is required for validation of this neural mobilization concept, particularly in cervical radiculopathy [10, 13].

Many studies have been done on the treatment of cervical radiculopathy. But most of them are inconclusive in terms of defining appropriate treatment options that would be efficacious for the treatment of this pathology [9].

The purpose of this study was to assess the neural mobilization technique as an effective treatment to improve neck mobility, and reduce pain intensity and disability for cervical radiculopathy through appropriate randomized controlled trials, taking the factors and outcome measures under consideration that are not addressed properly in previous literature.

Material and methods

This was a parallel-group randomized controlled trial with a 1:1 allocation ratio into two groups. The study was conducted at the physical therapy department of Mayo Hospital Lahore. This randomized trial was conducted according to consolidated standards of reporting trial CONSORT guidelines (2010) [14] from July 2019 to July 2020 as mentioned in Fig 1. Ethical approval was gained from the University of Lahore (Ref#IRB-UOL-FAHS/373-VI/2018). Written informed contents in Urdu or English were taken from all the subjects to participate in the study. The trial was prospectively registered through the Iranian Registry of Clinical Trials (IRCT20190325043109N1) on 30/6/2019. Total 88patients (44 in Group 1 and 44 in group 2) were included through the convenience sampling technique in this study, using an effect size of 0.70, using (mean ±SD) in group 1(neural mobilization group) (3.35±1.49) and group 2 (exercise group) (4.45±1.63), at the level of significance 0.05 and power 9 0% [15]. To recruit the patients in this study, patients between ages 35–50 years, of both genders, having radiating symptoms of cervical radiculopathy from at least 2 months and not more than 6 months (for the diagnosis of the patients with cervical radiculopathy clinical predictor rule was applied consisting of Spurling’s test, Distraction test, upper limb nerve tension test ULNTT for the median nerve and ipsilateral neck rotation), with no previous cervical surgeries, no loss of the upper limb movement and willing to participate were chosen. Subjects having traumatic history, osteoporosis, hypermobility, circulatory disturbances, tumor-causing cervical radiculopathy and who were not willing were excluded from the study. Patients were asked to sign a consent form and give their will regarding being enrolled in the study.

Fig 1. Consort flow diagram.

Fig 1

Randomization and concealment of allocation

The randomization sequence was created by using Excel 2016 with a 1:1 allocation using simple randomization by an independent researcher who was not participating in the treatment of patients.

Patients were allocated to two groups by concealment of allocation (sealed envelopes).

Allocation concealment was achieved with sequentially numbered, opaque, sealed, envelopes SNOSE. SNOSE was used according to the guidelines of Doig and Simpson [16].

An independent researcher with no clinical involvement in the trial made the concealed envelopes. 88 Envelopes were made. Half envelopes contained folded papers with Treatment A (group 1) written on them and the remaining half contained folded papers with Treatment B (group 2) written on them. A unique randomized number was allocated to these envelopes and shuffled vigorously. Then envelopes were arranged sequentially and handed over to another independent researcher. The assessor pre-tested the participant and to eligible subjects, the envelope was allocated to the subject. The therapist recorded the information on the envelope and opened it afterward to maintain the concealment. The assessor recorded the post-treatment findings and another independent analyst analyzed the data.

Blinding

In this study patients, assessors, and data analysts were blinded to the allocation of treatment groups in this study. Except for the therapist, all other staff was kept blinded as they were not informed about the details of allocation. The trial adhered to established procedures to maintain separation between the staff who was collecting outcome measurements and the therapist. Patients were blinded to treatment allocation as treatment was given in separate rooms for each group. A therapist who is not blinded did not take the outcome measurements. All the other assessors, investigators, and analysts did not know the details of treatment.

Intervention

All the subjects were given hot packs for 10 minutes before the treatment in both groups.

Subjects fulfilling the sample selection criteria were given treatment for 12 sessions (3 times per week for 4 weeks). Pre-assessment was done at baseline, the second assessment was done after 2 weeks and the final post-assessment was done at the end of the 12th session in the 4th week in both groups. Fig 1 has provided a detailed description of the participant’s flow through the study.

Group 1

In this group neural mobilization technique with sliding of the median nerve was applied in 1 set of 10 repetitions with 3 seconds hold in each repetition. Neural mobilization was done according to the technique described by David Butler [16]. The subject was placed in supine position with the shoulder in abduction and lateral rotation; elbow in extension, forearm in supination and wrist, finger and thumb in extension position then finally, to apply the stretch shoulder was taken in greater abduction and cervical spine in contralateral side flexion.

In this group conservative treatment was also given which included 3 sets of cervical isometrics exercises with 10 repetitions in each direction with 5 seconds hold in each isometric movement and 30 seconds rest period between each set. Isometric exercises were performed with the patient in a sitting position. For the cervical flexor isometrics, the therapist placed his hand on the anterior side of the patient’s forehead, and the patient was instructed to push his head against the therapist’s hand in the forward direction, for the cervical extensor isometrics, the therapist placed his hand on the posterior side of the patient’s head and was instructed to push the head in the backward direction, for the cervical side flexors therapist placed his hand on the lateral sides (both right and left) of patient’s head and the patient was instructed to push sideways and for the cervical rotator, the isometrics therapist placed his hand on the lateral side of the patient’s head(both right and left) and instructed him to rotate the head.

Group 2

In group 2 conservative treatments were given which included cervical isometrics exercises with 10 repetitions in each direction, with 5 seconds hold in each isometric movement, 3 sets of these exercises were performed with the rest period of 30 seconds.

Isometric exercises were performed with the patient in a sitting position with a similar procedure mentioned in group 1

Outcome measures

The main outcome was to measure the effectiveness of the neural mobilization technique on pain intensity measured on NPRS, range of motion measured on inclinometer, and measuring the effects of treatment on quality of life measured through Neck Disability Index (NDI).

The numeric pain rating scale (NPRS) is an 11point scale ranging from 0 to 10, and a higher score indicates greater intensity of pain. 0 stands for no pain and 10 for worst possible pain. In subjects with neck pain, NPRS has ICC = 0.67 [17]. The inclinometer is a device used for measuring angles and the cervical range of motion Inclinometer has ICC = 0.85 [18].

NDI is a self-reported questionnaire used for measuring functional status in subjects with neck pain, the questionnaire contains a total of 10 sections and for each section, the total possible score is 5: if the first statement is marked the section score = 0 if the last statement is marked it = 5. If all ten sections are completed the score is calculated by the following formula: Score: /50 Transform to percentage score x 100 = %points.

The lesser score represents a lesser disability or better functional status, and NDI has fair test-retest reliability [19].

Baseline measurements

Patient age, gender, baseline pain, ROM, and quality of life were noted at the time of recruitment.

Data analysis

Data were analyzed using SPSS version 21. Descriptive analyses (mean, variance, standard deviation) were performed for quantitative data. Frequencies and percentages were calculated for categorical and nominal data of gender. Data were analyzed for normality by applying Shapiro- Wilk test. To compare the variables between both groups, independent samples t-test was used for cervical ranges and Mann-Whitney U test was used for NPRS and NDI. To compare the variable within groups, repeated measure ANOVA was used for cervical ranges and the Friedman test was used for NPRS and NDI. P-value ≤ 0.05 was considered significant. Intention to treat analysis with the technique of last observation carried forward (LOCF) was used to handle the missing data due to loss of follow-up.

Results

Total of 88 subjects were included in this study, 5 patients (2 from group 1 and 3 from group 2) were lost to follow-up, mostly due to the ongoing pandemic situation, and missing data were managed through intention to treat analysis with the technique of last observation carried forward. The mean age of the subject in group 1 was 41.09± 6.05in and group 2 was 42.22 ± 5.62. According to the gender distribution in the neural mobilization group, 15 (34.1%) were males and 29 (65.9%) were females and in the conventional treatment group, 13 (29.5%) were males and 31 (70.5%) were females.

Shapiro-Wilk test of normality has shown that p values were greater than 0.05 for cervical range of motion variables and less than 0.05 for neck disability index (NDI) and numeric pain rating scale (NPRS), showing that data was normally distributed for cervical range of motion (ROM) and not normally distributed for NDI and NPRS. Pretreatment comparison of variables (NPRS, NDI, and cervical ROM) between both groups showed that there was no statistically significant difference between both groups at the baseline as presented in Tables 1 and 2.

Table 1. Baseline measurement of pain (NPRS) and disability (NDI).

Variable At Baseline
Neural mobilization group Conservative treatment group Z score p-value
Mean rank Mean rank
NPR 44.89 44.11 -0.14 0.88
NDI 42.84 46.16 -0.61 0.54

Table 2. Baseline measurement of cervical range of motion (ROM).

Variable At baseline
Neural mobilization group Conservative treatment group Mean Change (95% CI) p-value
Mean ± SD. Mean ± SD.
Cervical flexion 39.09± 9.41 38.54± 11.48 0.55(-3.90,4.99) 0.80
Cervical extension 39.06± 12.26 42.04± 12.23 2.97(-8.16,2.21) 0.25
Cervical right side flexion 29.81± 8.46 30.81± 10.21 1.00(-4.97, 2.97) 0.61
Cervical left side flexion 29.88± 8.82 30.36± 8.55 0.47(-4.16, 3.20) 0.79
Cervical right rotation 36.45± 10.36 38.38± 9.58 1.93(-6.16, 2.29) 0.36
Cervical left rotation 40.09± 9.09 40.90± 10.50 0.81(-4.98, 3.34) 0.69

Comparison of variable with in group 1 has shown that there was a statistically significant difference between pre, mid, and post-treatment NPRS scores. Χ2 = 82.14, p<0.001. Post hoc analysis with Wilcoxon signed-rank was conducted with Bonferroni correction applied, resulting in a significant level set at p < 0.017. The Median (interquartile range (IQR)) for pretreatment the in experimental group NPRS score was 6(5 to 6), mid-treatment was 4 (3 to 5) and post-treatment was 3 (2 to 4). There was a significant difference between pretreatment and mid-treatment (Z = -5.76, p<0.001), mid-treatment and post-treatment (Z = -5.46, p<0.001), and pretreatment and post-treatment (Z = -5.74, p<0.001), showing that NPRS score was significantly improved after 2 weeks and further improved after 4 weeks of treatment in the experimental group as shown in Table 3.

Table 3. Comparison of pain (NPRS), disability (NDI), and cervical mobility (ROM) within the experimental group.

Variable Baseline 2nd week follow up At the end of the 4th week Χ2 / F p-Value
NPRS 6(5 to 6) 4 (3 to 5) 3 (2 to 4) Χ2 = 82.14 < 0.001*
Median (IQR)
NDI 38(30 to 46) 24 (20 to 28) 14 (8.5 to 20) Χ2 = 71.30 < 0.001*
Median (IQR)
Cervical flexion 39.09± 9.41 44.65 ±8.30 48.22± 8.89 F = 78.94 0.01**
Mean ± S.D
Cervical extension 39.06± 12.26 45.65 ±12.74 49.56 ±13.09 F = 66.69 < 0.001
Mean ± S.D
Cervical right side flexion 29.81± 8.46 34.29 ±8.84 37.93 ±9.06 F = 153.99 < 0.001
Mean ± S.D
Cervical left side flexion 29.88± 8.82 35.18± 9.05 39.31± 9.10 F = 132.76 < 0.001
Mean ± S.D
Cervical right rotation 36.45± 10.36 43.02 ±10.12 46.88 ±10.21 F = 75.52 < 0.001
Mean ± S.D
Cervical left rotation 40.09± 9.09 45.38± 9.39 49.06 ±9.45 F = 108.85 < 0.001
Mean ± S.D

* Friedman test

** Repeated measure ANOVA (for all cervical ranges)

There was a statistically significant difference between pre, mid, and post-treatment NDI score.

Χ2 = 71.302, p<0.001. Post hoc analysis with Wilcoxon signed-rank was conducted with Bonferroni correction applied, resulting in a significant level set at p < 0.017. The Median (IQR) for pretreatment Neck Disability Score (NDI) in the experimental group was 38(30 to 46), mid-treatment was 24 (20 to 28) and post-treatment was 14 (8.5 to 20). There was a significant difference between pretreatment and mid-treatment (Z = -5.41, p<0.001), mid-treatment and post-treatment (Z = -5.68, p<0.001), and pretreatment and post-treatment (Z = -5.58, p<0.001), showing that disability was significantly reduced after 2 weeks and further reduce after 4 weeks of treatment in the experimental group.

Pre and post-treatment comparison of cervical ranges of motion score in experimental has shown that post-treatment mean and standard deviation improved with p < 0.05, showing that neural mobilization is effective in improving cervical ranges in patients with cervical radiculopathy as shown in Table 3.

Comparison of variables within the group 2 has shown that there was a statistically significant difference between pre, mid, and post-treatment NPRS scores. Χ2 = 71.02, p = 0.00. Post hoc analysis with Wilcoxon signed-rank was conducted with Bonferroni correction applied, resulting in a significant level set at p < 0.017. Median (IQR) for pretreatment in the control group NPRS score was 6(5 to 6), mid-treatment was 5 (3.25 to 6) and post-treatment was 4 (2.25 to 5). There was a significant difference between pretreatment and mid-treatment (Z = - 5.38, p = 0.00), mid-treatment and post-treatment (Z = -4.74, p<0.001), and pretreatment and post-treatment (Z = -5.49, p<0.001), showing that NPRS score was significantly improved after 2 weeks and further improved after 4 weeks of treatment in the control group.

There was a statistically significant difference between pre, mid, and post-treatment NDI scores, Χ2 = 72.11, p<0.001. Post hoc analysis with Wilcoxon signed-rank was conducted with Bonferroni correction applied, resulting in a significant level set at p < 0.017. The Median (IQR) for pretreatment Neck Disability Score (NDI) in the control group was 40(30 to 49), mid-treatment was 30 (22 to 38) and post-treatment was 22 (16 to 30). There was a significant difference between pretreatment and mid-treatment (Z = -5.23, p<0.001), mid-treatment and post-treatment (Z = -5.26, p<0.001), and pretreatment and post-treatment (Z = -5.51, p<0.001), showing that disability was significantly reduced after 2 weeks and further reduce after 4 weeks of treatment in the control group.

Pre and post-treatment comparison of cervical ranges of motion score in group 2 has shown that post-treatment mean and standard deviation improved with p < 0.05, showing that conventional treatment is effective in improving cervical ranges in patients with cervical radiculopathy as shown in Table 4.

Table 4. Comparison of pain (NPRS), disability (NDI), and cervical mobility (ROM) within the control group.

Variable Baseline 2nd week follow up At the end of the 4th week Χ2 / F p-Value
NPRS 6(5 to 6) 5 (3.25 to 6) 4 (2.25 to 5) Χ2 = 71.02 < 0.001*
NDI 40 (30 to 49) 30 (22 to 38) 22 (16 to 30) Χ2 = 72.11 < 0.001*
Cervical flexion 38.54± 11.48 44.06 ±8.74 47.63± 7.62 F = 54.28 < 0.001**
Cervical extension 42.04± 12.23 48.09 ±9.20 50.27 ±8.79 F = 32.17 < 0.001
Cervical right side flexion 30.81± 10.21 33.77 ±8.04 36.31 ±7.69 F = 25.78 < 0.001
Cervical left side flexion 30.36± 8.55 34.09± 6.65 36.38± 6.92 F = 33.60 < 0.001
Cervical right rotation 38.38± 9.58 42.70 ±9.64 45.54 ±9.97 F = 54.97 < 0.001
Cervical left rotation 40.90± 10.50 43.86± 9.61 45.88 ±9.44 F = 33.55 < 0.001

*Friedman test

** Repeated measure ANOVA

A comparison of the mean and standard deviation of NPRS between group 1 and group 2 has shown that there was no significant difference in NPRS score at baseline, as value p>.05, but there was significant difference after 2nd and further improvement after 4th week, as value p < .05, showing that neural mobilization is more effective in reducing pain.

A comparison of NDI between group 1 and group 2 has shown that there was no significant difference in NDI score at baseline and even after 2 weeks of treatment, as value p>.05, but there was a significant difference after 4 weeks in the neural mobilization group as the mean rank was 35.30 with p<0.05 as shown in Table 5.

Table 5. Comparison of NPRS and NDI between the experimental and control group.

Variable At Baseline At the end of 4th week
Neural mobilization group Conservative treatment group Z score p-value Neural mobilization group Conservative treatment group Z score p-value
Mean rank Mean rank
Mean rank Mean rank
NPRS 44.89 44.11 -0.14 0.88 37.45 51.55 -2.63 0.008
NDI 42.84 46.16 -0.61 0.54 35.30 53.70 -3.38 0.001

Comparison of the mean and standard deviation of cervical range of motion between group 1 and group 2 has shown, that there was no significant difference in cervical ranges at baseline, after 2nd and 4th weeks of treatment, as p-value >.05, so experimental and control groups showed equal improvement as shown in Table 6.

Table 6. Comparison of cervical range of motion between experimental and control group.

Variables At baseline At the end of 4th week
Neural mobilization group Conservative treatment group Mean Change (95% CI) p-value Neural mobilization group Conservati ve treatment group Mean Change (95%CI) p-value
Mean±SD. Mean±SD. Mean±SD. Mean±SD.
Cervical 39.09± 38.54± 11.48 0.55(- 0.80 48.22± 8.89 47.63± 0.59 (- 0.73
flexion 9.41 3.90,4. 7.62 2.92,
99) 4.10)
Cervical 39.06± 42.04± 12.23 2.97(- 0.25 49.56 50.27 0.70(- 0.76
extension 12.26 8.16,2. ±13.09 ±8.79 5.43,
21) 4.02)
Cervical 29.81± 30.81± 10.21 1.00(- 0.61 37.93 ±9.06 36.31 1.61(- 0.37
right side 8.46 4.97, ±7.69 1.95 to
flexion 2.97) 5.17)
Cervical 29.88± 30.36± 8.55 0.47(- 0.79 39.31± 9.10 36.38± 2.93(- 0.93
left side 8.82 4.16, 6.92 0.46 to
flexion 3.20) 6.35)
Cervical 36.45± 38.38± 9.58 1.93(- 0.36 46.88 45.54 1.34(- 0.53
right 10.36 6.16, ±10.21 ±9.97 2.93 to
rotation 2.29) 5.61)
Cervical 40.09± 40.90± 10.50 0.81(- 0.69 49.06 ±9.45 45.88 3.18(- 0.11
left 9.09 4.98, ±9.44 0.82 to
rotation 3.34) 7.18)

Discussion

Cervical radiculopathy is a clinical syndrome, that often affected persons are unable to perform their social obligations, do physical tasks pertinently, and lose working hours [20]. In literature for cervical radiculopathy many non-surgical treatment options are discussed and multimodal conservative approach has been proven to be more effective in improving the symptoms [21].

Subjects with cervical radiculopathy show deconditioning of cervical muscles due to inactivity. Exercises are shown to be beneficial in improving well-being of a person and reducing disability. These has also shown to improve sleep, emotional and physical functioning, cognitive functioning, and reducing depression or anxiety [22]. In present study neural mobilization was used along with strengthening exercises of cervical muscles. This showed results in consistent with Liang et al, as it showed improvement in range of motion of cervical spine and reduction in pain [10]. Past studies show the moderate benefit of these exercises in reducing pain and improving strength in patients with cervical radiculopathy [2]. Exercises promote analgesic effect in musculoskeletal pain, as shown in the study of Lima et al exercises can reduce the hyperalgesia in muscle pain or after an injury. These results are corelate with the present study as reduction in pain is observed in both groups [23]. This exercise-induced hypoalgesia or analgesia predicts greater pain relief and improvement in cervical functioning by restoring muscular balance through strengthening cervical muscle exercises, this in turn impacts the quality of life positively, enhancing independence and reducing disability [22]. In the present study, comparison of NDI score between group 1 and group 2 has shown that there was significant improvement (p<0.05) in NDI score in group 1 with neuro-mobilization while the comparison of NPRS between group 1 and group 2 has also shown there was a significant difference after 2nd and further improved after 4th week, as value p < .05, showing that neural mobilization is more effective in reducing pain and improving functional status in cervical radiculopathy. Many other studies also support these results as exercise intervention containing isometric exercise of deep neck flexor muscles showed alleviation in levels of pain and disability, measured on outcome scale of numeric pain rating scale NPRS and neck disability index NDI respectively [2427]. In present study both groups were given hot fermentation along with exercise regime. This treatment program when combined with heating modalities, shows decreased pain in patients with cervical radiculopathy as shown in a randomized controlled trial of Diab et al. [28].

In addition to strengthening exercises, neurophysiological and analgesic effect of neural mobilization also predicts relief in pain and improvement in cervical functioning. Mechanism of pain reduction is by stimulating mechanical receptors, reducing edema and improving circulation [29]. Results of present study also correlate with a study conducted by Boyle et al. and Beniciuk et al in which the effects of manual physical therapy including neural mobilization were assessed on cervical radiculopathy. These studies concluded that mechanistic effects of neural mobilization differ from sham treatment, it resulted in neurophysiological effect and hypoalgesia of C-mediated fibers and there was a reduction in sensory descriptors. Results showed improvement in range of cervical motion, alleviation in cervical pain, improvement in disability, and enhancing functional capacity of the patients. Significant improvements were shown on NDI and NPRS [30], which are consistent with the present study as pre and post-treatment comparison of NDI scores in group 1 has shown that neural mobilization is effective in improving functional status in patients of cervical radiculopathy [31].

Results of present study are also in consistent with study of Dong-Gyu et al. which compared effects of neural-mobilization with manual cervical traction on pain, disability, muscle endurance and range of motion in individuals with cervical radiculopathy. As in present study these outcomes were improved in group treated with neural-mobilization along with cervical isometric exercises [13].

In a randomized trial of Kim et al, the patient showed improvement in NPRS, NDI, range of motion and endurance of deep flexor cervical muscles in patients with cervical radiculopathy [13]. Results of the presents study have shown that cervical ranges were significantly improved in both groups (p<0.05) but a comparison of cervical range of motion between group 1 and group 2 has shown, that there was no significant difference in cervical ranges after 4 weeks of treatment, as p-value >.05, so experimental and control groups showed almost equal improvement.

From the literature, it seems that multimodal management interventions are more effective than uni-modal strategies. Among non-surgical conservative multimodal management comprised of neurodynamic mobilization and exercises are more effective as conservative treatment in participants with cervical radiculopathy [8, 32].

In present study an effort has been made to consider all the elements of high-quality evidence so knowledge base could be improved about the effective treatment options for cervical radiculopathy. However, further research is required focusing on reducing the variability in patient selection in clinical trials, which will further optimize clinical practice. Therefore, there are a few limitations in this study that may affect the results and should be considered in future studies. First, when given combined treatment it is often times difficult to interpret the result of a single intervention. Second, subjective or objective measurement of upper limb pain and numbness due to radiculopathy were not included. Third, the sample was collected only from one clinical setting so results cannot be generalized. Fourth, this study is biased in using neural mobilization technique on median nerve, therefore this technique may not be useful for participants with cervical radiculopathy at other cervical spinal levels. Fifth, long term effects should be evaluated in future studies.

Conclusion

The present study concludes that neural mobilization combined with cervical isometrics is more effective as treatment program for patients with cervical radiculopathy in reducing pain, increasing cervical range of motion, and reducing neck disability, than cervical isometric exercises alone.

Implication

Being cost-effective treatment technique and non-availability of different expensive modalities in most clinical settings, this study will help many people with cervical radiculopathy and can enhance the scope of rehabilitation in these subjects.

Supporting information

S1 Checklist. Consolidated standards of reporting trials checklist.

(DOCX)

S1 File. Study protocol.

(DOCX)

S2 File. Synopsis.

(DOCX)

S1 Data. Study data.

(XLSX)

Acknowledgments

I would like to express my deep gratitude to Professor Humayun Zafar, my research supervisor, for their patient guidance, enthusiastic encouragement, and useful critiques of this research work.

Data Availability

All relevant data are within the paper and its Supporting Information files.

Funding Statement

The authors received no specific funding for this work.

References

  • 1.Eubanks JD. Cervical radiculopathy: nonoperative management of neck pain and radicular symptoms. Am Fam Physician. 2010;81(1):33–40. [PubMed] [Google Scholar]
  • 2.Iyer S, Kim HJ. Cervical radiculopathy. Curr Rev Musculoskelet Med. 2016;9(3):272–80. doi: 10.1007/s12178-016-9349-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Schmid AB, Fundaun J, Tampin B. Entrapment neuropathies: a contemporary approach to pathophysiology, clinical assessment, and management. Pain Rep. 2020;5(4):e829. doi: 10.1097/PR9.0000000000000829 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Kim HJ, Nemani VM, Piyaskulkaew C, Vargas SR, Riew KD. Cervical Radiculopathy: Incidence and Treatment of 1,420 Consecutive Cases. Asian Spine J. 2016;10(2):231–7. doi: 10.4184/asj.2016.10.2.231 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Guthold R, Ono T, Strong KL, Chatterji S, Morabia A. Worldwide variability in physical inactivity a 51-country survey. Am J Prev Med. 2008;34(6):486–94. doi: 10.1016/j.amepre.2008.02.013 [DOI] [PubMed] [Google Scholar]
  • 6.Muhammad U, Naeem A, Badshah M, Amjad I. Effectiveness of cervical traction combined with core muscle strengthening exercises in cervical radiculopathy. Journal Of Public Health and Biological Sciences. 2012;1:115–20. [Google Scholar]
  • 7.Nasca RJ. Cervical radiculopathy: current diagnostic and treatment options. J Surg Orthop Adv. 2009;18(1):13–8. [PubMed] [Google Scholar]
  • 8.Thoomes EJ. Effectiveness of manual therapy for cervical radiculopathy, a review. Chiropr Man Therap. 2016;24:45. doi: 10.1186/s12998-016-0126-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Plaza-Manzano G, Cancela-Cilleruelo I, Fernández-de-Las-Peñas C, Cleland JA, Arias-Buría JL, Thoomes-de-Graaf M, et al. Effects of Adding a Neurodynamic Mobilization to Motor Control Training in Patients With Lumbar Radiculopathy Due to Disc Herniation: A Randomized Clinical Trial. Am J Phys Med Rehabil. 2020;99(2):124–32. doi: 10.1097/PHM.0000000000001295 [DOI] [PubMed] [Google Scholar]
  • 10.Liang L, Feng M, Cui X, Zhou S, Yin X, Wang X, et al. The effect of exercise on cervical radiculopathy: A systematic review and meta-analysis. Medicine (Baltimore). 2019;98(45):e17733. doi: 10.1097/MD.0000000000017733 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Ojoawo AO, Olabode AD. Comparative effectiveness of transverse oscillatory pressure and cervical traction in the management of cervical radiculopathy: A randomized controlled study. Hong Kong Physiother J. 2018;38(2):149–60. doi: 10.1142/S1013702518500130 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Basson A, Olivier B, Ellis R, Coppieters M, Stewart A, Mudzi W. The effectiveness of neural mobilizations in the treatment of musculoskeletal conditions: a systematic review protocol. JBI Database System Rev Implement Rep. 2015;13(1):65–75. doi: 10.11124/jbisrir-2015-1401 [DOI] [PubMed] [Google Scholar]
  • 13.Kim DG, Chung SH, Jung HB. The effects of neural mobilization on cervical radiculopathy patients’ pain, disability, ROM, and deep flexor endurance. J Back Musculoskelet Rehabil. 2017;30(5):951–9. doi: 10.3233/BMR-140191 [DOI] [PubMed] [Google Scholar]
  • 14.Schulz KF, Altman DG, Moher D, the CG. CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials. BMC Medicine. 2010;8(1):18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Faul F, Erdfelder E, Lang AG, Buchner A. G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods. 2007;39(2):175–91. doi: 10.3758/bf03193146 [DOI] [PubMed] [Google Scholar]
  • 16.Butler DS. The neurodynamic techniques: a definitive guide from the Noigroup team: Noigroup publications; 2005. [Google Scholar]
  • 17.Young Ia Pt D, Dunning J Pt DPT, Butts R Pt P, Mourad F Pt DPT, Cleland Ja Pt P. Reliability, construct validity, and responsiveness of the neck disability index and numeric pain rating scale in patients with mechanical neck pain without upper extremity symptoms. Physiother Theory Pract. 2019;35(12):1328–35. doi: 10.1080/09593985.2018.1471763 [DOI] [PubMed] [Google Scholar]
  • 18.de Koning CH, van den Heuvel SP, Staal JB, Smits-Engelsman BC, Hendriks EJ. Clinimetric evaluation of active range of motion measures in patients with non-specific neck pain: a systematic review. Eur Spine J. 2008;17(7):905–21. doi: 10.1007/s00586-008-0656-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Young IA, Cleland JA, Michener LA, Brown C. Reliability, construct validity, and responsiveness of the neck disability index, patient-specific functional scale, and numeric pain rating scale in patients with cervical radiculopathy. Am J Phys Med Rehabil. 2010;89(10):831–9. doi: 10.1097/PHM.0b013e3181ec98e6 [DOI] [PubMed] [Google Scholar]
  • 20.Caridi JM, Pumberger M, Hughes AP. Cervical radiculopathy: a review. Hss j. 2011;7(3):265–72. doi: 10.1007/s11420-011-9218-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Kuligowski T, Skrzek A, Cieślik B. Manual Therapy in Cervical and Lumbar Radiculopathy: A Systematic Review of the Literature. Int J Environ Res Public Health. 2021;18(11). doi: 10.3390/ijerph18116176 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Busch AJ, Webber SC, Richards RS, Bidonde J, Schachter CL, Schafer LA, et al. Resistance exercise training for fibromyalgia. Cochrane Database Syst Rev. 2013;2013(12):Cd010884. doi: 10.1002/14651858.CD010884 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Saragiotto BT, Maher CG, Yamato TP, Costa LOP, Costa LCM, Ostelo R, et al. Motor Control Exercise for Nonspecific Low Back Pain: A Cochrane Review. Spine (Phila Pa 1976). 2016;41(16):1284–95. doi: 10.1097/BRS.0000000000001645 [DOI] [PubMed] [Google Scholar]
  • 24.Cheng CH, Tsai LC, Chung HC, Hsu WL, Wang SF, Wang JL, et al. Exercise training for non-operative and post-operative patient with cervical radiculopathy: a literature review. J Phys Ther Sci. 2015;27(9):3011–8. doi: 10.1589/jpts.27.3011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Cleland JA, Whitman JM, Fritz JM, Palmer JA. Manual physical therapy, cervical traction, and strengthening exercises in patients with cervical radiculopathy: a case series. J Orthop Sports Phys Ther. 2005;35(12):802–11. doi: 10.2519/jospt.2005.35.12.802 [DOI] [PubMed] [Google Scholar]
  • 26.Kjaer P, Kongsted A, Hartvigsen J, Isenberg-Jørgensen A, Schiøttz-Christensen B, Søborg B, et al. National clinical guidelines for non-surgical treatment of patients with recent onset neck pain or cervical radiculopathy. Eur Spine J. 2017;26(9):2242–57. doi: 10.1007/s00586-017-5121-8 [DOI] [PubMed] [Google Scholar]
  • 27.de Campos TF, Maher CG, Steffens D, Fuller JT, Hancock MJ. Exercise programs may be effective in preventing a new episode of neck pain: a systematic review and meta-analysis. J Physiother. 2018;64(3):159–65. doi: 10.1016/j.jphys.2018.05.003 [DOI] [PubMed] [Google Scholar]
  • 28.Diab AA, Moustafa IM. The efficacy of forward head correction on nerve root function and pain in cervical spondylotic radiculopathy: a randomized trial. Clin Rehabil. 2012;26(4):351–61. doi: 10.1177/0269215511419536 [DOI] [PubMed] [Google Scholar]
  • 29.Cui XJ, Yao M, Ye XL, Wang P, Zhong WH, Zhang RC, et al. Shi-style cervical manipulations for cervical radiculopathy: A multicenter randomized-controlled clinical trial. Medicine (Baltimore). 2017;96(31):e7276. doi: 10.1097/MD.0000000000007276 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Boyles R, Toy P, Mellon J Jr., Hayes M, Hammer B. Effectiveness of manual physical therapy in the treatment of cervical radiculopathy: a systematic review. J Man Manip Ther. 2011;19(3):135–42. doi: 10.1179/2042618611Y.0000000011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Beneciuk JM, Bishop MD, George SZ. Effects of upper extremity neural mobilization on thermal pain sensitivity: a sham-controlled study in asymptomatic participants. J Orthop Sports Phys Ther. 2009;39(6):428–38. doi: 10.2519/jospt.2009.2954 [DOI] [PubMed] [Google Scholar]
  • 32.De Pauw R, Kregel J, De Blaiser C, Van Akeleyen J, Logghe T, Danneels L, et al. Identifying prognostic factors predicting outcome in patients with chronic neck pain after multimodal treatment: A retrospective study. Man Ther. 2015;20(4):592–7. doi: 10.1016/j.math.2015.02.001 [DOI] [PubMed] [Google Scholar]

Decision Letter 0

Walid Kamal Abdelbasset

5 Oct 2022

PONE-D-22-23496Effectiveness of Neural Mobilization on Pain, Range of motion, and Disability in Cervical Radiculopathy: A Randomized Controlled TrialPLOS ONE

Dear Dr. Rafiq,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

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Walid Kamal Abdelbasset, Ph.D.

Academic Editor

PLOS ONE

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https://www.sciencedirect.com/science/article/abs/pii/S1521694215000297?via%3Dihub

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[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

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Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Partly

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: I Don't Know

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Please make the following modifications to the paper:

1. Please revise the study title in light of the current study's objectives.

2. Work on balancing the different sections of the research abstract, as the method and results sections are clearly overly detailed.

3. I hope the author(s) will be as brief as possible in these two sections of the abstract - methods and results - with a focus on the most important research findings in the results section of the study abstract.

4. The introduction is far too long and detailed. I hope to limit the introduction to two or three paragraphs at most, with the final paragraph devoted to the current research problem and how to solve it within the framework of the current study's design objective.

5. I noticed that the material and method sections were written as paragraphs with side headings. The names of the side headings, in my opinion, are ineffective in describing what is related to them in this section, which the author(s) should change.

6. Please relate Figure 1 to the texts in the material and methods section.

7. The author(s) should carefully review the progress of their research results to avoid the presence of statistical flaws, some of which were discovered while reviewing the paper, with the goal of displaying graphic images to alleviate the boredom caused by displaying the results only in the style of statistical tables.

8. Author(s) should also avoid using side titles in the results section, which is not recommended.

9. I noticed that the discussion section served as an introduction to the study, and the discussion appeared to be completely inadequate in terms of proving or denying the current study's findings with previous studies, so please review this shortcoming.

10. In the final paragraph of the discussion, consider emphasizing the study's future trends, as well as its strengths and weaknesses.

11. Rewrite the conclusion section in the context of resolving the research problem and clarifying the study's goal achievement.

12. Updating the reference list and replacing outdated references prior to 2015 with new ones.

13. In general, the paper requires linguistic correction to eliminate grammatical errors and typos.

//Good luck//

Reviewer #2: In the first comment, all pages have no number and no line numbers so it is very difficult to detect the pages in the consort checklist and lines in the manuscript

This manuscript requires a significant amount of improvement, the authors have designed a randomized controlled study to show the effectiveness of the neural mobilization technique on cervical radiculopathy which has already been studied more times in the past by other researchers as the author wrote in the last paragraph of introduction,

� I already read reference No 9 in the last paragraph which is completely against the fact you write (Liang, Long PhDa,b; Feng, Minshan PhDa,b; Cui, Xin MSa; Zhou, Shuaiqi MSa,b; Yin, Xunlu PhDa,b; Wang, Xingyu MDc; Yang, Mao MDc; Liu, Cunhuan MDd; Xie, Rong MDa; Zhu, Liguo PhDa,b,∗; Yu, Jie PhDa,b,∗; Wei, ,

Introduction

Need editing and rewrite

Methods:

� What is the novelty of your method and measurement?

� The treatment time was very short without follow up

� The arrangement of the method is very weak and you should follow the consort checklist

Statistics

� Completely Not clear –please rewrite again and discuss which test you used and why

� all tables need to rearrange

� Outcomes and estimation need to be explained well

Discussion:

needs to be as per well defined objectives

Describe sources of potential bias and imprecision

It has to be framed in such a way that readers are able to have good understanding of the current evidences and rationale of the paper

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

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Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

**********

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PLoS One. 2022 Dec 6;17(12):e0278177. doi: 10.1371/journal.pone.0278177.r002

Author response to Decision Letter 0


24 Oct 2022

I am grateful to the reviewers for their insightful comments on the paper. We have been able to incorporate changes to reflect most of the suggestion provided by the reviewers. Here is a point-by-point response to the reviewer’s comments and concerns.

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

Guidelines has been followed during development of manuscripts.

2. We noticed you have some minor occurrence of overlapping text with the following previous publication, which needs to be addressed:

Reference of the article has been given in methodology.

3. Thank you for stating the following financial disclosure:

No specific funding was received for this research.

4. We note that you have indicated that data from this study are available upon request. PLOS only allows data to be available upon request if there are legal or ethical restrictions on sharing data publicly. For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions.

All relevant data is available within the manuscript. Data cannot be shared publicly because of ethical concerns. Patients were included on a no objection base to conduct the study. Patients were not asked for permission to publish full encrypted data.

In your revised cover letter, please address the following prompts:

a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent.

b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. Please see http://www.bmj.com/content/340/bmj.c181.long for guidelines on how to de-identify and prepare clinical data for publication. For a list of acceptable repositories, please see http://journals.plos.org/plosone/s/data-availability#loc-recommended-repositories.

We will update your Data Availability statement on your behalf to reflect the information you provide.

Data availability statement has been updated on the cover page

5. We noted in your submission details that a portion of your manuscript may have been presented or published elsewhere. Please clarify whether this [conference proceeding or publication] was peer-reviewed and formally published. If this work was previously peer-reviewed and published, in the cover letter please provide the reason that this work does not constitute dual publication and should be included in the current manuscript.

This article is present in the pre-prints and was mentioned in the cover letter and link is as follow https://www.researchsquare.com/article/rs-223383/v1 . One other article containing different variables were extracted from this research and is published recently in BioMed journal; link is as follow https://www.hindawi.com/journals/bmri/2022/9385459

6. Your ethics statement should only appear in the Methods section of your manuscript. If your ethics statement is written in any section besides the Methods, please delete it from any other section.

Remove it from abstract and check in methodology

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Partly

________________________________________

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: I Don't Know

________________________________________

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

________________________________________

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

________________________________________

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Please make the following modifications to the paper:

1. Please revise the study title in light of the current study's objectives.

Study title has been revised.

2. Work on balancing the different sections of the research abstract, as the method and results sections are clearly overly detailed.

Method and results sections are revised.

3. I hope the author(s) will be as brief as possible in these two sections of the abstract - methods and results - with a focus on the most important research findings in the results section of the study abstract.

Method and results sections in abstract are revised.

4. The introduction is far too long and detailed. I hope to limit the introduction to two or three paragraphs at most, with the final paragraph devoted to the current research problem and how to solve it within the framework of the current study's design objective.

Information in introduction section has been curtailed.

5. I noticed that the material and method sections were written as paragraphs with side headings. The names of the side headings, in my opinion, are ineffective in describing what is related to them in this section, which the author(s) should change.

Methodology of other published articles in PLOS one is carefully reviewed. In this article subheadings are given where necessary to describe details of methodology.

6. Please relate Figure 1 to the texts in the material and methods section.

Figure 1 has been mentioned in the text of material and methods.

7. The author(s) should carefully review the progress of their research results to avoid the presence of statistical flaws, some of which were discovered while reviewing the paper, with the goal of displaying graphic images to alleviate the boredom caused by displaying the results only in the style of statistical tables.

I have carefully reviewed the result section but were unable to find the statistical flaws. It would be of great if you could point out what kind of flaws has been noticed.

8. Author(s) should also avoid using side titles in the results section, which is not recommended.

Side titles in the results section has been removed.

9. I noticed that the discussion section served as an introduction to the study, and the discussion appeared to be completely inadequate in terms of proving or denying the current study's findings with previous studies, so please review this shortcoming.

Discussion has been rewritten and effort has been made to rectify all shortcomings.

10. In the final paragraph of the discussion, consider emphasizing the study's future trends, as well as its strengths and weaknesses.

Limitations, strength and weaknesses of the study are mentioned at end of discussion section.

11. Rewrite the conclusion section in the context of resolving the research problem and clarifying the study's goal achievement.

Conclusion has been rewritten.

12. Updating the reference list and replacing outdated references prior to 2015 with new ones.

New references have been added

Reviewer #2: In the first comment, all pages have no number and no line numbers so it is very difficult to detect the pages in the consort checklist and lines in the manuscript

This manuscript requires a significant amount of improvement, the authors have designed a randomized controlled study to show the effectiveness of the neural mobilization technique on cervical radiculopathy which has already been studied more times in the past by other researchers as the author wrote in the last paragraph of introduction,

� I already read reference No 9 in the last paragraph which is completely against the fact you write (Liang, Long PhDa,b; Feng, Minshan PhDa,b; Cui, Xin MSa; Zhou, Shuaiqi MSa,b; Yin, Xunlu PhDa,b; Wang, Xingyu MDc; Yang, Mao MDc; Liu, Cunhuan MDd; Xie, Rong MDa; Zhu, Liguo PhDa,b,∗; Yu, Jie PhDa,b,∗; Wei, ,

Study of Liang et al. concluded that Exercise alone or exercise plus other treatment may be helpful to patients with Cervical radiculopathy. However, exercise option should be carefully considered for each patient with CR. Large-scale studies using proper methodology are recommended that is why in our study carefully designed exercise plan was incorporated in both treatment groups and neural mobilization was additionally added in group 1 to measure its effectiveness. Result of our studies corelate with this study as both groups shows the significant improvement but adding neural mobilization was more helpful in improving pain and functional status.

Introduction

Need editing and rewrite

Introduction section has been edited.

Methods:

� What is the novelty of your method and measurement?

� The treatment time was very short without follow up

This has been mentioned in the limitations of study.

� The arrangement of the method is very weak and you should follow the consort checklist

Statistics

� Completely Not clear –please rewrite again and discuss which test you used and why

� all tables need to rearrange

� Outcomes and estimation need to be explained well

Description of the test used for the analysis is mentioned under the data analysis heading and is as follow:

Normality testing has shown that data were normally distributed for the variable “cervical range of motion” so parametric tests were used for the within (repeated measure ANOVA) and between group comparison

Data were skewed for the variable NPRS and NDI so non parametric tests were used for the within (Friedman Test) and between (Mann Whitney U test) group comparison

Intention to treat analysis with the technique of last observation carried forward (LOCF) was used to handle the missing data due to loss of follow-up.

Discussion:

needs to be as per well defined objectives

Describe sources of potential bias and imprecision

It has to be framed in such a way that readers are able to have good understanding of the current evidences and rationale of the paper

Discussion section has been revised.

________________________________________

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

Attachment

Submitted filename: Reviwer COMMENTS.docx

Decision Letter 1

Walid Kamal Abdelbasset

4 Nov 2022

PONE-D-22-23496R1Comparison of Neural Mobilization and Conservative treatment on Pain, Range of motion, and Disability in Cervical Radiculopathy: A Randomized Controlled TrialPLOS ONE

Dear Dr. Rafiq,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

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We look forward to receiving your revised manuscript.

Kind regards,

Walid Kamal Abdelbasset, Ph.D.

Academic Editor

PLOS ONE

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

Reviewer #3: (No Response)

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2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: No

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3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: No

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4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: Yes

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5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: No

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6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Dear Author(s),

Thank you for your efforts in incorporating the improvements I proposed in the article, and best wishes.

Regards,

Reviewer #2: thanks alot for your responses

Reviewer #3: This randomized clinical trial was designed to compare the effectiveness of neural mobilization with conservative treatment on pain intensity, cervical range of motion, and disability. The conclusions are unclear.

Overall assessment: All the statistical methods used for the analysis have not been specified in the Data Analysis section. Additionally, the wording is oftentimes unclear, leading to incorrect interpretations by the reader.

Major and minor revisions:

1- Abstract: Provide a brief description of the statistical methods used to compare and express the difference within and between the groups.

2- Data Analysis section:

a. Mann-Whitney U test is misspelled.

b. This section is unclear. What comparisons were made with repeated measures ANOVA? With the Friedman tests?

3- Results section:

a. Specify the type of summary statistic that follows the +/- signs. Both variance and standard deviation are noted in the methods section.

b. Shapiro-Wilks p-values were “greater than” 0.05, would be the standard terminology.

c. Be specify, “for mostly” is too vague.

d. In the Data Analysis section, state the type of statistical method used to estimate the p-values in Tables 1 and 2. Be transparent.

e. The results show a chi-square result. List and describe the use of this method in the Data Analysis section.

f. In the Data Analysis section, list and describe all the statistical methods used.

g. Use consistent notation, for instance SD and S.D has been used. The standard is SD.

h. All acronyms and abbreviations must be spelled out at first mention.

3- Ask a native English speaker to proofread the document to improve its clarity.

4- To assist in the review process, please add line numbers to the document.

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Reviewer #1: No

Reviewer #2: No

Reviewer #3: No

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PLoS One. 2022 Dec 6;17(12):e0278177. doi: 10.1371/journal.pone.0278177.r004

Author response to Decision Letter 1


6 Nov 2022

I am grateful to the reviewers for their insightful comments on the paper. We have been able to incorporate changes to reflect most of the reviewers’ suggestions. The text is a point-by-point response to the reviewer’s comments and concerns.

1-Abstract: Provide a brief description of the statistical methods used to compare and express the difference within and between the groups.

A brief description of the statistical method used has been added in the abstract section.

2- Data Analysis section:

a. Mann-Whitney U test is misspelled.

The spelling has been corrected

b. This section is unclear. What comparisons were made with repeated measures ANOVA? With the Friedman tests?

The p-values of the Shapiro-Wilk normality test were greater than 0.05 for cervical ranges but less than 0.05 for NDI and NPRS, showing that data were normality distributed for the cervical range of motions but not normally distributed for NPRS and NDI.

To assess the difference within the group, a parametric test i.e., repeated measure ANOVA was used for cervical ranges but its non-parametric counterpart i.e., Friedman test was used for NPRS and NDI.

To assess the difference between the group, a parametric test i.e., independent sample t was used for cervical ranges but its non-parametric counterpart i.e., Mann-Whitney U was used for NPRS and NDI.

3- Results section:

a. Specify the type of summary statistic that follows the +/- signs. Both variance and standard deviation are noted in the methods section.

b. Shapiro-Wilks p-values were “greater than” 0.05, would be the standard terminology.

Corrected

c. Be specify, “for mostly” is too vague.

Corrected

d. In the Data Analysis section, state the type of statistical method used to estimate the p-values in Tables 1 and 2. Be transparent.

Table 1 and 2 shows the difference between group 1 and 2 at baseline. P values in table 1 are of the Mann Whitney U test and table 2 are of the independent sample t-test.

e. The results show a chi-square result. List and describe the use of this method in the Data Analysis section.

The Chi-square test was not used, table 3 and 4 provide the test statistic (χ2) value ("Chi-square"), and the significance level ("Asymp. Sig."), which we need to report the result of the Friedman test.

f. In the Data Analysis section, list and describe all the statistical methods used.

All the statistical methods used are mentioned in data analysis section

g. Use consistent notation, for instance SD and S.D has been used. The standard is SD.

Corrected

h. All acronyms and abbreviations must be spelled out at first mention.

Corrected

Attachment

Submitted filename: response to reviewer.docx

Decision Letter 2

Walid Kamal Abdelbasset

14 Nov 2022

Comparison of Neural Mobilization and Conservative treatment on Pain, Range of motion, and Disability in Cervical Radiculopathy: A Randomized Controlled Trial

PONE-D-22-23496R2

Dear Dr. Rafiq,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

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Kind regards,

Walid Kamal Abdelbasset, Ph.D.

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

Reviewer #3: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: (No Response)

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: (No Response)

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: (No Response)

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

Reviewer #3: (No Response)

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Dear author(s),

Thank you for including the arbitrators' required amendments in the paper.

Best wishes,

Reviewer #2: thanks for your response

Reviewer #3: (No Response)

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7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

Reviewer #3: No

**********

Acceptance letter

Walid Kamal Abdelbasset

23 Nov 2022

PONE-D-22-23496R2

Comparison of Neural Mobilization and Conservative treatment on Pain, Range of motion, and Disability in Cervical Radiculopathy: A Randomized Controlled Trial

Dear Dr. Rafiq:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Walid Kamal Abdelbasset

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Checklist. Consolidated standards of reporting trials checklist.

    (DOCX)

    S1 File. Study protocol.

    (DOCX)

    S2 File. Synopsis.

    (DOCX)

    S1 Data. Study data.

    (XLSX)

    Attachment

    Submitted filename: Reviwer COMMENTS.docx

    Attachment

    Submitted filename: response to reviewer.docx

    Data Availability Statement

    All relevant data are within the paper and its Supporting Information files.


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