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A diagnostic tool for people with lumbar instability: a criterion-related validity study

Abstract

Background

Several clinical tests used to identify patients with lumbar instability have reported diagnostic accuracy in separate studies with conflicting results. To augment the diagnostic process, tests that are better able to identify lumbar instability suitable for use in the clinical setting are required. The aim of this study was to identify the probability to diagnose patients with lumbar instability, using x-ray imaging as the reference standard.

Methods

This study was a cross-sectional, diagnostic validity study. One hundred forty participants with chronic low back pain underwent an x-ray assessment and 14 clinical examinations. Data were analysed using multivariate regression methods to determine which clinical tests were most diagnostic for lumbar instability when they were applied together.

Results

Eighteen (12.85%) participants had radiological lumbar instability. Three clinical tests i) interspinous gap change during flexion-extension, ii) passive accessory intervertebral movement tests, iii) posterior shear test demonstrated an ability to diagnose lumbar instability of 67% when they were all positive. At this probability threshold, sensitivity, specificity, positive likelihood ratio (+LR), and negative likelihood ratio (−LR) were 5.56, 99.18%, 6.78, and 0.95.

Conclusions

These 3 clinical tests could be useful in identifying patients with lumbar instability in the general community. These three tests are simple to perform by physical therapists, reliable to use in a clinical setting, and safe for patients. We recommend physical therapists use these three tests to assess patients who are suspected of having lumbar instability, in the absence of an x-ray assessment, to receive appropriate targeted intervention or referral for further investigation.

Trial registration

Thai Clinial Trial Registry (TCTR 20180820001; 19th August 2018).

Peer Review reports

Background

Lumbar spinal stability is the ability of the lumbar spine to tolerate displacement during normal physiological postures and loads without the generation of nociceptive stimuli [1, 2]. Lumbar spine stability is achieved through the combination of three control subsystems; passive, active and neural control [2]. When at least one of these subsystems is compromised, lumbar spine movement can become abnormal [3], which can be detected through qualitative and quantitative assessments [4], such as self-reporting of symptoms and radiographic techniques [5, 6].

Lumbar instability has been identified in up to 57% of patients with chronic low back pain (CLBP) via X-ray [7]. The incidence rate of clinical lumbar instability in patients with CLBP is 13-46% [8, 9]. Lumbar instability can lead to pain, functional limitations and reduced quality of life [10,11,12], as well as further develop into spondylolisthesis in certain cases, which may require surgical treatment [1, 13]. Therefore, the prompt detection of lumbar instability is crucial to preventing disease progression or inhibiting adverse effects. Appropriate conservative treatment, such as exercise stabilization, which focuses on deep trunk muscle training, can improve or delay the development of lumbar instability [14,15,16,17]. In order to identify patients who can benefit from specific therapy, clinical decision-making is based on the accuracy of clinical examinations [13, 18, 19].

Flexion-extension X-ray is used to identify lumbar instability [1, 19]. However, it can only detect a loss of integrity in the passive subsystem, which is characterized by the excessive movement of one vertebra on another [19]. Additional limitations of X-ray-based diagnosis include the administration cost, accessibility, time cost and radiation exposure [13, 20]. A variety of clinical tests have been introduced to diagnose lumbar instability. Previous studies have investigated the diagnostic accuracy of several of these tests by comparing them to X-rays [7, 19, 21,22,23,24]. Treatment-based classification has been used to identify patients likely to benefit from stabilization exercises [25]. Previous studies have reported that the accuracy among tests varied widely, with sensitivity values of 5-84% and specificity values of 3-100% [7, 21,22,23,24]. Therefore, drawing any conclusions about the superiority of one test over another is difficult. To the best of our knowledge, diagnostic accuracy has so far been reported for 14 lumbar instability tests in separate studies with conflicting results [7, 21,22,23,24,25]. However, in a clinical setting, the physical therapist cannot perform 14 clinical tests, due to time constraints. Therefore, in order to improve the diagnostic process, the tests that are better able to identify lumbar instability and are suitable for the average clinical setting need to be determined. This study intends to investigate the predictive probability of the 14 instability tests to assess which tests are most suitable.

Two previous studies have reported the use of multivariate regression analysis in clinical examinations for the diagnosis of lumbar instability [7, 25]. The first study reported hypermobility in the passive accessory intervertebral movements test and a lumbar flexion range of > 53°. These two tests exhibited a high specificity of 98.0% and a positive likelihood ratio (+LR) of 12.8 [7]. The second study reported a specificity of 86.0% and a + LR of 4.0 when at least three of the following criteria were met: prone instability test, positive aberrant motion test, average straight leg raise (SLR) of > 91° and age of < 40 years [25].

A study by Areeudomwong et al. [9] reported a combination of four tests for classifying lumbar instability as follows: apprehension sign, instability catch sign, painful catch sign and prone instability test. When at least 3/4 of these tests were positive, a sensitivity of 47.8% and specificity of 91.7% were recorded [9].

However, due to the limited evidence available and the fact that previous research is based on patients from hospital settings with a narrow age range, such as 45-67 years [21], 56-80 years [23], 43-68 years [24] and 41-59 years [9], the generalizability of these results to people with CLBP may be limited. Calculating measures of effect from predicted probabilities following logistic regression is an appropriate method to infer the overall source population from which the study sample was drawn [26]; however, this has not been done to date.

The purpose of the present study was to examine the relationship between 14 clinical tests, obtained from prior studies [7, 21,22,23,24,25] and X-ray findings for patients with CLBP in community-based health settings, in order to establish the probability of existing lumbar instability across a wide age range (20–60 years). This could inform treatment decision-making without having to rely on radiography, as access to X-rays may be limited. In addition, this test can provide supporting information to justify the referral of patients to X-ray services for further examination.

Materials and methods

Methods

The study protocol for human research was approved by The Human Research Ethics Committee of Khon Kaen University, Thailand according to the declaration of Helsinki (HE 602379). The study was prospectively registered at Thai Clinical Trials Registry (TCTR 20180820001).

Participants

According to Long [27], and Voorhis and Morgan [28], a minimum of 10 participants per parameter is a sufficient number for a logistic regression model. As the current study included 14 clinical tests, the sample size target was 140 CLBP participants aged 20-60 years with or without pain radiation into the lower extremities that lasted > 3 months.

Potential participants were recruited via posters and social media advertisements in a community-based setting. The selection of participants was undertaken using a convenience sampling approach. The exclusion criteria included the following; contraindication to X-ray assessment (e.g., pregnancy), previous lumbar surgery, serious spinal pathology (e.g., cauda equina syndrome, malignancy, vertebral fracture and infection), scoliosis, neurological deficit and spondylolisthesis [12, 29].

Procedure

Prior to the main data collection, 16 participants with CLBP were assessed by a physical therapist who conducted the 14 clinical assessments to evaluate intra-rater reliability. The main study participants were assessed at 2 sessions.

During the first session, participants signed the consent form and the investigators collected their demographic data [age, sex, Roland Morris Disability Questionnaire (RMDQ) [30], body mass index and pain information]. Participants were asked about pain duration, pain radiation, whether they were currently undergoing a pain episode, and the average pain score in the last 24 h; 14 clinical assessments were then conducted (Additional file 1).

During the second session, participants were evaluated by an orthopaedic surgeon who ordered an X-ray assessment. Six views were used for plain radiographs; anteroposterior, lateral, two oblique, lateral flexion, and lateral extension with participants positioned in side-lying. The X-ray procedure was completed by a radiologist. The lateral flexion-extension radiographs were then inspected for lumbar instability by a trained observer.

X-ray measurement technique

All X-ray images for each participant were read by a trained observer who was blinded to the clinical test results. Imaging-related findings have been previously used to confirm the presence of lumbar instability [7, 12, 21,22,23,24]. The amount of sagittal plane translation and rotation occurring at individual spinal motion segments between L1-2 and L5-S1 was calculated from the X-ray films (Fig. 1) [12].

Fig. 1
figure 1

Measurement technique of lumbar instability [12]. Angulation: Two straight lines are draw along the inferior endplate of the upper vertebra and the superior endplate of the lower vertebra. The intersection of these two lines is angulation in flexion (Ɵ−) and in extension (Ɵ+). The difference of intervertebral angles between Ɵ− and Ɵ+ is amount of rotational instability. Translation: The straight line is drawn bisect the angulation in flexion (Ɵ−) and in extension (Ɵ+). The difference between the two distances from flexion (A) and extension (B) is amount of translation

The reference value of lumbar instability was defined as a translation of > 4.5 mm at L1-2 to L5-S1 and rotation of > 15° at L1-2, L2-3 and L3-4, of > 20° at L4-5, and of > 25° at L5-S1 [31]. The participants was considered to have lumbar instability when (i) two segments exhibited rotation or translation instability, or when (ii) one segment exhibited both translation and rotation instability [7, 12].

Data analysis

Descriptive statistics were calculated and sequestered into groups of participants with and without a diagnosis of lumbar instability, as diagnosed using X-ray. Continuous variables were compared using independent t-tests and categorical variables using Pearson’s χ2 tests. A significance level of P < 0.05 was used for all variables.

The reliability of X-rays and clinical examination variables was examined. Kappa coefficients were used for dichotomous variables and intraclass correlation coefficients (ICC) (3, 1) were used for continuous variables.

Univariate and multivariate logistic regression were used to analyse the predictive test of lumbar instability. The clinical tests that reached a P < 0.2 in the univariate analysis were considered to be associated with lumbar instability and were entered into the first model of multivariate regression analysis. P < 0.2 was selected in order to prevent missing any clinical tests that might be associated with lumbar instability [32, 33].

Backward stepwise elimination was used to build the model. During each of the backward stepwise techniques, pseudo-R-squared and goodness of fit test [Akaike information criterion (AIC), Bayes information criterion and area under the curve (AUC)] were conducted to compare the performance of each model. The model with the lowest AIC value was considered to be the best one [34]. Moreover, P < 0.05 was considered significant in the final model, and the variables retained were used to develop the probability to diagnose existing lumbar instability. Data analysis was conducted using STATA 10.0 (StataCorp LP; College Station, TX, USA).

Results

A total of 140 participants with CLBP were included in the present study; a STARD flow chart can be seen in Fig. 2.

Fig. 2
figure 2

STARD flow diagram

The patients’ demographic characteristics are described in Table 1; of the 140 participants, 12.86% had lumbar instability and 87.14% did not. The majority of variables were not different between the two groups. Only the RMDQ was significantly (P = 0.04) higher in the lumbar instability group. The mean difference in the RMDQ score was 2.58, which was less than the minimal clinical important difference of 3.5 [35].

Table 1 Demographic characteristics of the 140 participants with and without lumbar instability

A total of 18 (12.86%) participants had lumbar instability. Their average age was 37.0 ± 12.32 years (range, 20-53 years), with 13 women and 5 men. When classified into age groups, 6 (33%) were aged 20-29 years, 4 (22%) 30-39 years, 2 (11%) 40-49 years and 6 (33%) 50-59 years.

Among of the 47 segments, the most commonly recorded levels of instability were L4-5 (n = 20; 42.55% of segments), L5-S1 (n = 13; 27.66% of segments), L2-3 (n = 7; 14.89% of segments), L3-4 (n = 6; 12.77% of segments) and L1-2 (n = 1; 2.13% of segments).

Sagittal rotation and translation were compared between participants with and without lumbar instability (Fig. 3). Rotation instability was significantly greater at the L2-3, L3-4 and L4-5 levels (P < 0.05) in participants with lumbar instability. For translation, this was significantly greater at L4-5 and L5-S1 levels (P < 0.05) in the lumbar instability group.

Fig. 3
figure 3

Comparison of sagittal rotation (a) and tanslation (b) in participant with and without lumbar instability

The ICC of the X-ray measurement technique was 0.83 (95% CI: 0.46-0.96) for rotation and 0.93 (95% CI: 0.74-0.98) for translation, suggesting a good measurement consistency. The Kappa coefficient of the 14 clinical tests ranged from moderate to excellent (Table 2). Three tests demonstrated moderate reliability [‘passive physiological intervertebral movements (PPIVMs) (flexion)’, ‘passive lumbar extension test’ and ‘aberrant motion test’]. Four tests demonstrated good reliability [‘passive accessory intervertebral movements’ (PAIVMs), ‘painful catch sign’, ‘posterior shear test’ and ‘interspinous gap change’]. The ‘total trunk extension’, ‘lumbar flexion’, ‘Beighton’s scale’, ‘PPIVMs (extension)’, ‘prone instability test’, ‘sit to stand’ and ‘average SLR’ tests exhibited excellent reliability [36, 37].

Table 2 Reliability coefficients of 14 clinical examinations (n = 16)

The univariate regression analyses results are presented in Table 3. The interspinous gap change, PAIVMs, PPIVMs (flexion), PPIVMs (extension), painful catch sign and posterior shear tests reached a P < 0.2, which suggested a good to excellent reliability (Table 2).

Table 3 Univariate analyses

Six tests were therefore selected for the initial model of multivariate logistic regression. The backward stepwise technique was used to eliminate one clinical test per model. Pseudo-R-squared and four types of goodness of fit test were performed for each model (Table 4). The final model underwent the interspinous gap change, PAIVMs and posterior shear tests, since they had the lowest AIC and a good AUC. Moreover, the Hosmer-Lemeshow test reached a P = 0.33, which suggested that the model fit the data reasonably well [38].

Table 4 The characteristic of each model during backward stepwise technique

To confirm the combination of the three clinical tests as the final model, multivariate analysis was performed with P < 0.05 (Table 5).

Table 5 Multivariate analyses

Based on the final model of the multivariate logistic regression analysis, the probability of having lumbar instability can be calculated as \(\mathrm{Prob}\left(\mathrm{lumbar}\ \mathrm{instability}=1\right)=\frac{1}{1+{\mathrm{e}}^{-\left(-5.37+1.75\left(\mathrm{X}1\right)+2.63\left(\mathrm{X}2\right)+1.69\left(\mathrm{X}3\right)\right)}}\). The X1, X2 and X3 were replaced with 0 (negative result) and 1 (positive result) in the interspinous gap change, PAIVMs and posterior shear test. When the three tests were positive, the predictive model produced a 67% probability of patients with CLBP having lumbar instability. At this predictive threshold, sensitivity, specificity, +LR, and -LR were 5.56% (95% CI: 0.14-27.30), 99.18% (95% CI: 95.5-100), 6.78 (95% CI: 0.44-104) and 0.95 (95% CI: 0.85-1.07), respectively.

Discussion

To the best of our knowledge, this was the first study to investigate the predictive probability of clinical tests in patients with lumbar instability. When used in combination, a positive result from three clinical tests (interspinous gap change, PAIVMs and posterior shear tests) indicated a probability of 67% for the presence of lumbar instability in patients.

Study participants with lumbar instability were similar to clinical populations in that they were mostly middle-aged females with instability at the L4-5 level [7, 21,22,23,24]. However, when considering the age group of patients with lumbar instability, a similar number of patients with lumbar instability were aged 20-29 and 50-59 years. This result suggested that physical therapists should also look out for lumbar instability in young patients with CLBP.

In the present study, the percentage (12.86%) of CLBP patients with lumbar instability in the study population was lower than previously reported (57%) [7]. This may have been due to the wide age range (20-60 years) of participants in this, compared to previous, studies, since lumbar instability has been found to be more prevalent in individuals aged > 40 years [7, 21,22,23,24]. In addition, the lumbar instability criteria in the present study were more comprehensive than those of earlier studies, in an attempt to minimize the number of false-positive X-rays reported in earlier studies [7]. Finally, this study included individuals with CLBP drawn from a community sample, as opposed to the hospital-based samples of previous studies [7, 21,22,23,24].

The present study reported that patients with lumbar instability typically had a longer duration of symptoms and a higher frequency of pain radiation, compared with those without lumbar instability. However, whilst there was a statistical difference in the RMDQ between the groups, this was less than the minimal clinical important difference. The disability score of participants with lumbar instability was higher in this study than that in earlier studies [7, 23]. As reported by previous studies, instability was more frequently observed at the L4-5 level, which was due to the orientation of the zygapophyseal joint being inclined in the sagittal plane [21, 24].

In the present study, a full flexion-extension X-ray in a side-lying position was used to avoid the influence of muscle bracing and aggravation of the patient’s pain during movement while standing [12, 39,40,41]. These postures produced a significantly higher rotation (at the L2-3, L3-4 and L4-5 levels) and translation (at the L4-5 and L5-S1 levels) in participants with lumbar instability, compared with those without lumbar instability. These results highlighted the possibility that excessive lumbar movement was not only induced in standing and seated flexion-extension, but also in lateral side-lying flexion-extension, which was consistent with previous findings [12, 39,40,41].

Regression analysis showed that the three clinical tests in the final model fit the data well and had a satisfactory reliability range (from good to moderate). These findings confirm that these three tests related to test the passive stability subsystem. It was shown herein that, when all three tests were positive, the probability of having lumbar instability was 67%, with the sensitivity, specificity, +LR and -LR at 5.56, 99.18%, 6.78 and 0.95, respectively. Thus, the combination of these three tests can predict lumbar instability with a high specificity (99%) and a moderate +LR (6.78) [42]. Furthermore, the final model had an AUC of 0.78, which indicated an adequate discriminative ability between patients with CLBP who have and do not have lumbar instability [38].

A high sensitivity (82.2%), moderate specificity (60.7%), and low +LR (2.1) and -LR (0.3) have been reported for the interspinous gap change test, which was developed by Ahn and Jung [24]. The interspinous gap change test was undertaken in a standing position with lumbar spine flexion-extension performed passively through the hip joint. Excessive movements at the end of lumbar spine flexion-extension were due to passive subsystem dysfunction, leading to an inability to control spine movement within the normal range.

PAIVMs are commonly utilized when physical therapists identify movement abnormalities in the lumbar spine, be that joint hyper- or hypomobility [22]. This technique has been assessed during the absence of muscle activation, with the passive stability of the lumbar spine being the target for the test [43]. In the present study, increasing movement was observed at the degenerative region, suggesting that the restraining structures cannot limit the displacement of that lumbar segment. Abbott et al. [22] reported that PAIVMs had a high specificity (89%) and low sensitivity (29%), which was consistent with the results of Fritz et al. [7], who reported a specificity of 81% and sensitivity of 46%.

Fritz et al. (2005) reported that the posterior shear test has a low diagnostic accuracy [7], which was inconsistent with the present findings. Although both studies used the same test protocol, it is unclear why the result was different. One possible reason for this could be a variation in the force applied by the examiner to the participant’s abdomen [7]. The examiner of the current study may have applied greater force compared to the examiner used in the study by Fritz et al. [7], leading to a positive posterior shear test result in the present study.

The three predictive tests in this study had a higher specificity when used as indicative tests of passive subsystem dysfunction, compared with previous studies [7, 22, 24]. Furthermore, to the best of our knowledge, the present study was the first to use predictive probability, AIC and AUC to support the test results. These tests could provide valuable information for physical therapists during the clinical assessment of patients with CLPB suspected of having lumbar instability. However, while the combination of the three tests exhibited a satisfactory reliability and high specificity, which would enable the physical therapist to identify patients who are very likely to have lumbar instability, their low sensitivity may not help rule out the diagnosis of lumbar instability.

Several clinical tests, such as aberrant motion, sit to stand, lumbar flexion and prone instability tests, were not found to be associated with instability, as expected. As all the tests were active movement tests, it can be speculated that, when there is passive subsystem dysfunction, the remaining subsystems (active and neural control) provide a compensatory change, thus influencing spinal stability [3, 44]. Therefore, patients may not exhibit instability signs during these tests.

The findings of the present study can prove useful for clinicians. However, the study was not without its limitations. First, the prevalence of lumbar instability was smaller than expected. Although, the sample size was calculated using the rule of thumb, had a power of 0.98 and was considered acceptable [45] a sample size that includes a higher percentage of participants with lumbar instability is recommended in further research. Secondly, pain in full flexion-extension may have led to a lower amount of translation and rotation instability than the actual amount experienced by the patients, although their position was adjusted by the radiologist. Thirdly, the current study design may not be recommended for the establishment of predictive tests; a longitudinal study design may instead help obtain more accurate results.

Conclusion

To the best of our knowledge, this was the first study that presented the probability of the three tests combination to predict lumbar instability in community-based patients with CLBP across a wide age range. Three clinical tests that assess the passive stability subsystem were found to predict lumbar instability with a satisfactory reliability. These tests were the interspinous gap change, PAIVMs and posterior shear test. When patients with CLBP have positive results on these three tests, there is a 67% probability that they suffer from lumbar instability.

Availability of data and materials

The data will be available for anyone who wishes to access them for any purpose. The data will be accessible from immediately following publication to 6 months after publication, and contact should be made via the Corresponding author rungthiprt@gmail.com.

Abbreviations

CLBP:

Chronic low back pain

RMDQ:

Roland Morris Disability Questionnaire

ICC:

Intraclass correlation coefficients

-LR:

Negative likelihood ratio

+LR:

Positive likelihood ratio

AIC:

Akaike information criterion

BIC:

Bayes information criterion

AUC:

Area under the curve

PAIVMs:

Passive accessory intervertebral movement tests

PPIVMs:

Passive physiological intervertebral movement tests

SLR:

Straight leg raise

References

  1. Leone A, Guglielmi G, Cassar-Pullicio VN, et al. Lumbar intervertebral instability: a review. Radiology. 2007;245(1):62–77.

    Article  PubMed  Google Scholar 

  2. Izzo R, Guarnieri G, Guglielmi G, et al. Biomechanics of the spine. Part I: spinal stability. Eur J Radiol. 2013;82:127–38.

    Article  PubMed  Google Scholar 

  3. Panjabi MM. Clinical spinal instability and low back pain. J Electromyogr Kinesiol. 2003;13(4):371–9.

    Article  PubMed  Google Scholar 

  4. Dupuis PR, Yong-Hing K, Cassidy JD, Kilkaldy-Willis WH. Radiologic diagnosis of degenerative lumbar instability spinal instability. Spine. 1985;10(3):262–76.

    Article  CAS  PubMed  Google Scholar 

  5. Cook C, Brismee JM, Sizer PS. Subjective and objective descriptions of clinical lumbar spine instability: a Delphi study. Man Ther. 2006;11:11–21.

    Article  PubMed  Google Scholar 

  6. Iguchi T, Kanemura A, Kasahara K, et al. Age distribution of three radiologic factors for lumbar instability: propable aging process of the instability with disc degeneration. Spine (Phila Pa 1976). 2003;28:2628–33.

    Article  Google Scholar 

  7. Fritz J, Piva SR, Childa JD. Accuracy of the clinical examination to predict radiographic instability of the lumbar spine. Eur Spine J. 2005;14(8):743–50.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Puntumetakul R, Yodchaisarn W, Emasithi A, Keawduangdee P, Chatchawan U, Yamauchi J. Prevalence and individual risk factors associated with clinical lumbar instability in rice farmers with low back pain. Patient Prefer Adherence. 2015;9:1–7.

    PubMed  Google Scholar 

  9. Areeudomwong P, Jirarattanaphochai K, Ruanjai T, Buttagat V. Clinical utility of a cluster of tests as a diagnostic support tool for clinical lumbar instability. Musculoskelet Sci Pract. 2020;50:102224.

    Article  PubMed  Google Scholar 

  10. Araujo A, Costa L, Oliveira C, et al. Measurement properties of the Brazilian-Portuguese version of the lumbar spine instability questionnaire. Spine. 2016;42:810–4.

    Article  Google Scholar 

  11. Saragiotto BT, Maher CG, New CH, et al. Clinimetric testing of the lumbar spine instability questionnaire. J Orthop Sports Phys Ther. 2018;22:1–24.

    Google Scholar 

  12. Chatprem T, Puntumetakul R, Boucaut R, Wanpen S, Chatchawan U. A screening tool for patients with lumbar instability: a criteria-related validity of Thai version. Spine. 2020;45(21):E1131–8.

    Article  Google Scholar 

  13. Alqarni AM, Schneiders AG, Hendrick PA. Clinical test to diagnose lumbar instability: a systematic review. J Orthop Sports Phys Ther. 2011;41(3):130–40.

    Article  PubMed  Google Scholar 

  14. Kumar SP. Efficacy of segmental stabilization exercise for lumbar segmental instability in patients with mechanical low back pain: a randomized placebo-controlled crossover study. N Am J Med Sci. 2011;3:456–61.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Puntumetakul R, Areeudomwong P, Emasithi A, et al. Effect of 10-week core stabilization exercise training and detraining on pain-related outcomes in patients with clinical lumbar instability. Patient Prefer Adherence. 2013;7:1189–99.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Javadian Y, Behtash H, Akbari M, et al. The effects of stabilizing exercises on pain and disability of patients with lumbar segmental instability. J Back Musculoskelet Rehabil. 2012;25:149–55.

    Article  PubMed  Google Scholar 

  17. Javadian Y, Akbari M, Talebi G, et al. Influence of core stability exercise on lumbar vertebral instability in patients presented with chronic low back pain: a randomized clinical trial. Caspian J Intern Med. 2015;6:98–102.

    PubMed  PubMed Central  Google Scholar 

  18. Fritz J, Wainner R. Examining diagnostic tests: an evidence-based perspective. Phys Ther. 2001;81(9):1546–64.

    Article  CAS  PubMed  Google Scholar 

  19. Ferrari S, Manni T, Bonetti F, et al. A literature review of clinical tests for lumbar instability in low back pain: validity and applicability in clinical practice. Chiropr Man Therap. 2015;23(14):1–12.

    Google Scholar 

  20. Mülller-Schwefe G, Morlion B, Ahlbeck K, et al. Treatment for chronic low back pain: the focus should changes to multimodal management that reflects the underlying pain mechanisms. Curr Med Res Opin. 2017;33:1199–210.

    Article  Google Scholar 

  21. Maigne JY, Lapeyre E, Morvan G, et al. Pain immediately upon sitting down and relieved by standing up is often associated with radiologic lumbar instability or marked anterior loss of disc space. Spine. 2003;28(12):1327–34.

    Article  PubMed  Google Scholar 

  22. Abbott JH, McCane B, Herbison P, et al. Lumbar segmental instability: a criterion-related validity study of manual therapy assessment. BMC Musculoskelet Disord. 2005;6:56.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Kasai Y, Morishita K, Kawakita E, et al. A new evaluation method for lumbar spinal instability: passive lumbar extension test. Phys Ther. 2006;86:1661–7.

    Article  PubMed  Google Scholar 

  24. Ahn K, Jhun H-J. New physical examination tests for lumbar spondylolisthesis and instability: low midline sill sign and interspinous gap change during lumbar flexion-extension motion. BMC Musculoskelet Disord. 2015;16:97.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Hicks GE, Fritz JM, Delitto A, McGill SM. Preliminary development of a clinical prediction rule for determining which patients with low back pain will respond to a stabilization exercise program. Arch Phys Med Rehabil. 2005;86(9):1753–62.

    Article  PubMed  Google Scholar 

  26. Muller CJ, MacLehose RF. Estimating predicted probabilities from logistic regression: different methods correspond to different target populations. Int J Epidemiol. 2014;43(3):962–70.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Long SJ. Regression models for categorical and limited dependent variables. California: SAGE Publications, Inc.; 1997.

    Google Scholar 

  28. van Voorhis CW, Morgan BL. Statistical rules of thumb: what we don't want to forget about sample sizes. Psi Chi J. 2001;6(4):139–41.

    Article  Google Scholar 

  29. Cohen SP, Argoff CE, Carragee E. Management of low back pain. BMJ. 2009;338:100–6.

    Google Scholar 

  30. Jirarattanaphochai K, Sae-Jung S, Sumananont C, Saengnipanthkul S. Reliability of the Roland - Morris disability questionnaire (Thai version) for the evaluation of low back pain patients. J Med Assoc Thail. 2005;88(3):407–11.

    Google Scholar 

  31. White AA, Panjabi MM. Clinical biomechanics of the spine. 2nd ed. Philadelphia: Lippincott Company; 1990.

    Google Scholar 

  32. Marrone G, Abdul-Rahman L, de Coninck Zaake, et al. Predictors of contraceptive use among female adolescents in Ghana. Afr J Reprod Health. 2014;18(1):102–9.

    PubMed  Google Scholar 

  33. Sae-Jung S, Wongba N, Leurmprasert K. Predictive factors for neurological deficit in patients with spinal tuberculosis. J Orthop Surg. 2019;27(3):1–7.

    Article  Google Scholar 

  34. Burnham KP, Anderson DR. Model selection and multimodel inference: a practical information-theoretic approach. 2nd ed. New York: Springer-Verlag; 1998.

    Book  Google Scholar 

  35. Ostelo RW, de Vet HC. Clinically important outcomes in low back pain. Best Pract Res Clin Rheumatol. 2005;19(4):593–607.

    Article  PubMed  Google Scholar 

  36. Jewell D. Guide to evidence-based physical therapist practice. 2nd ed. Sudbury: Jones & Bartlett Learning; 2011.

    Google Scholar 

  37. Portney LG. Foundations of clinical research: applications to evidence-based practice. 4th ed. Philadelphia: F.A. David; 2020.

    Google Scholar 

  38. Hosmer DW, Lemshom S. Applied logistic regression. 2nd ed. New York: Wiley; 2000.

    Book  Google Scholar 

  39. Wood KB, Popp CA, Tranfeldt EE, et al. Radiographic evaluation of instability in spondylolisthesis. Spine. 1994;19:1697–703.

    Article  CAS  PubMed  Google Scholar 

  40. Landi A, Gregori F, Marotta N, et al. Hidden spondylolisthesis: unrecognized cause of low back pain? Prospective study about the use of dynamic projections in standing and recumbent position for the individuation of lumbar instability. Neuroradiology. 2015;57:58.

    Article  Google Scholar 

  41. Puntumetakul R, Saiklang P, Tapanya W, et al. The effects of core stabilization exercise with the abdominal drawing-in maneuver technique versus general strengthening exercise on lumbar segmental motion in patients with clinical lumbar instability: a randomized controlled trial with 12-month follow-up. Int J Environ Res Public Health. 2021;18:7811.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Kent P, Hancock M. Interpretation of dichotomous outcome: sensitivity, specificity, likelihood ratios, and pre-test probability. J Physiother. 2016;62(4):231–3.

    Article  PubMed  Google Scholar 

  43. Kulig K, Landel R, Powers CM. Assessment of lumbar spine kinematics using dynamic MRI: a proposed mechanism of sagittal plane motion induced by manual posterior-to-anterior mobilization. J Ortho Sports Phys Ther. 2004;34(2):57–64.

    Article  Google Scholar 

  44. Hicks GE, Fritz J, Delitto A, et al. Interrater reliability of clinical examination measurement for identification of lumbar segmental instability. Arch Phys Rehabil. 2003;84:1858–64.

    Article  Google Scholar 

  45. Norton BJ, Strube MJ. Understanding statistical power. J Orthop Sports Phys Ther. 2001;31(6):307–15.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This work was supported by the Royal Golden Jubilee (RGJ) Ph.D. Program, the Thailand Research Fund (TRF) number PHD/0193/2557, and the research center in Back, Neck, Other Joint Pain and Human performance (BNOJPH), Khon Kaen University, Khon Kaen, Thailand. Many thanks to Dr. Jitjira Chaiyarit, Department of Statistics, Faculty of Science, Khon Kaen University, for providing statistic support.

Funding

This work was supported by the Royal Golden Jubilee (RGJ) Ph.D. Program, the Thailand Research Fund (TRF) number PHD/0193/2557.

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Contributions

TC, RP, JK contributed to study design, data collection and data analysis, and drafted the manuscript; JS, GY contributed to review and editing the manuscript. All authors approved the final version of the manuscript and approved to be responsible for all aspects of the work.

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Correspondence to Rungthip Puntumetakul.

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Ethics approval and consent to participate

The Human Research Ethics Committee of Khon Kaen University, Thailand approved the study protocol in human research based on the declaration of Helsinki (HE 602379). The study was prospectively registered at Thai Clinical Trials Registry (TCTR 20180820001). Inclusion participants were provided with an explanation about the objectives and procedures of the study, and they were asked to sign an informed consent form prior to commencing the study.

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Not applicable.

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The authors declare that there is no completing interests.

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Supplementary Information

Additional file 1.

Methods of the 14 clinical examination.

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Chatprem, T., Puntumetakul, R., Kanpittaya, J. et al. A diagnostic tool for people with lumbar instability: a criterion-related validity study. BMC Musculoskelet Disord 22, 976 (2021). https://doi.org/10.1186/s12891-021-04854-w

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