- Research article
- Open Access
- Open Peer Review
The Mini-BESTest - a clinically reproducible tool for balance evaluations in mild to moderate Parkinson’s disease?
© Löfgren et al.; licensee BioMed Central Ltd. 2014
- Received: 15 April 2014
- Accepted: 1 December 2014
- Published: 12 December 2014
The Mini-BESTest is a clinical balance test that has shown a high sensitivity in detecting balance impairments in elderly with Parkinson's disease (PD). However, its reproducibility between different raters and between test occasions has yet to be investigated in a clinical context. Moreover, no one has investigated the reproducibility of the Mini-BESTest's subcomponents (i.e. anticipatory postural adjustments; postural responses; sensory orientation and dynamic gait).
We aimed to investigate the inter-rater and test-retest reproducibility (reliability as well as agreement) of the Mini-BESTest, as well as its subcomponents, in elderly with mild to moderate PD, performed under conditions assimilating clinical practice.
This was an observational measurement study with a test-retest design.
Twenty-seven individuals with idiopathic PD (66 - 80 years, mean age: 73; Hoehn & Yahr: 2-3; 1-15 years since diagnosis) were included. Two test administrators, having different experiences with the Mini-BESTest, administered the test individually, in separate rooms in a hospital setting. For the test-retest assessment, all participants returned 7 days after the first test session to perform the Mini-BESTest under similar conditions. Intra-class correlation coefficients (ICC2.1), standard error of measurement (SEMagreement), and smallest real difference (SRD) were analyzed.
The Mini-BESTest showed good reliability for both inter-rater and test-retest reproducibility (ICC = 0.72 and 0.80). Regarding agreement, the measurement error (SRD) was found to be 4.1 points (accounting for 15% of the maximal total score) for inter-rater reproducibility and 3.4 points (12% of the maximal total score) for test-retest reproducibility. The investigation of the Mini-BESTest's subcomponents showed a similar pattern for both inter-rater and test-retest reproducibility, where postural responses had the largest proportional measurement error, and sensory orientation showed the highest agreement.
Our findings indicate that the Mini-BESTest is able to distinguish between individuals with mild to moderate PD; however, when used in clinical balance assessments, the large measurement error needs to be accounted for.
- Measurement error
- Balance evaluation systems test
- Smallest real difference
Parkinson’s disease (PD), with a prevalence of more than 4 million people worldwide  and 22,000 in Sweden , is the second most common neurodegenerative disease. The incidence of PD, most common after the age of 60 years , rises with age and is expected to grow rapidly in the coming years . As the disease progresses, impaired balance control becomes one of the main features, interfering with physical independence  and quality of life ,. Out of the four cardinal symptoms in PD (tremor, bradykinesia, rigidity and postural instability), all but tremor are related to impaired balance control ,. Balance control in PD, being negatively affected from the early stages of the disease, includes impairments of postural responses as well as with turning and gait, and is also related to an increased risk of falling . It is therefore vital for a balance test to identify the array of problems that may occur in an individual with PD.
In order to help clinicians identify the specific balance problems, the Balance Evaluation Systems Test (BESTest)  was developed, addressing a variety of components influencing balance control. However, being very comprehensive, it has been regarded as too time consuming. Instead, this led to the development of the shortened, more clinically applicable version; the Mini-BESTest . This test addresses subcomponents of balance control, such as anticipatory postural adjustments, postural responses, sensory orientation and dynamic gait, and has been found to be sensitive in disclosing balance impairments among individuals with PD .
Reproducibility concerns the degree to which repeated measurements in study objects provide similar results, and can be divided into parameters of reliability or agreement . Whereas reliability measures aim to distinguish study objects from each other despite measurement errors, measures of agreement assesses the absolute measurement error of a test (i.e., the exact measurement error presented in the same units as the investigated item) ,. When investigating the reproducibility of a clinical test, there are various aspects to take into consideration. Sources of error for a test may depend upon the test administrator, the tested subject, the instrumentation and/or biological variability, as well as of the circumstances under which the test takes place ,. To gain fully accountable information regarding the reliability of a test, it is therefore important to take all possible sources of error into account. However, the prevailing approach for reproducibility investigations tend to be to use one person to act as a test administrator, being responsible for test instructions and the safety of the patient, and one or more other persons that observe and rate the test performance (by using the test instructions regarding how to grade the test performance). Although such an observational approach investigates the reproducibility of the test itself (by testing the actual grading scale), it lacks ecological validity because such conditions do not assimilate clinical practice. Indeed, the assessment of balance performance in clinical practice is a rather complex situation, with the clinician generally being responsible for giving the patients clear and concise instructions, as well as for the adequate interpretation (rating) of the test performance and the safety of the patient. Such a situation is also dependent on the relation between the clinician and the patient, that is, whether or not the patient trusts the clinician enough to perform challenging tasks adequately.
Previous studies have used the observational approach of investigating inter-rater reproducibility of the Mini-BESTest ,-, whereas others have used video recordings to rate the test retrospectively -. Such approaches differ from clinical test situations, making it difficult to generalize the results derived from these studies to clinical practice. Moreover, at times different physical therapists (with varied experience) may assess the balance abilities of a single patient before and after a rehabilitation period or at different stages in the health care system. Therefore, it may be important also to investigate the reproducibility of clinical tests that are performed by clinicians with different experience.
Recent studies have found the Mini-BESTest to be highly reproducible ,,,, but only one study focused on individuals with PD exclusively . In addition, the majority of these studies have reported their results only in form of the reliability parameter intra-class correlation (ICC). From a clinical perspective, this may be problematic, as the ICC score is a relative measure of reproducibility, thereby depending on the variance between subjects (i.e., the ICC score will be higher if there is much variability between subjects even if the variability between tests is high, and vice versa) ,. Therefore, the ICC score preferably should be complemented with measures of agreement (i.e., the exact number of points that are likely to reflect the measurement error), such as the standard error of measurement (SEM)  and the smallest real difference (SRD) . The SEM estimates an exact score that reflects the within subject error variance, and can be presented as SEMagreement (including systematic differences) or SEMconsistency (excluding systematic differences) . When the SEM is known, the SRD (reflecting the exact measurement error in a single individual) can be calculated .
Finally, as the reproducibility of the assessment may vary between different areas of balance control, it might also be of significance to investigate the reproducibility of each of the Mini-BESTest’s subcomponents. Our aim was therefore to investigate, in a clinical context, the inter-rater and test-retest reproducibility of the Mini-BESTest and its subcomponents in elderly with mild-to-moderate PD.
This study was designed as an observational measurement study with a test-retest design.
The Regional Board of Ethics in Stockholm (Dnr:2009/819-32, 2010/1472-32 and 2012/1829-32) provided their ethical approval of the study.
The participants were recruited from a balance intervention study (BETA-PD trial ) and provided their written informed consent to participate. However, none of the participants took part in any kind of physical intervention during the time of this study.
Inclusion criteria were a clinical diagnosis of “idiopathic” PD , Hoehn and Yahr stages 2 and 3, and ≥ 60 years of age. Participants were excluded if they had a diagnosis of other existing neurological disorders and/or medical conditions affecting balance control.
Participant demographics (n = 27)
Body mass index (weight/length2)
Time since diagnosis (years)
UPDRS motor score
Summary of the subcomponents and the items of the Mini-BESTest 1
Anticipatory postural adjustments 2
Sensory orientation 2
- Sit to stand
- Stance on firm surface; eyes open
- Rise to toes
- Stance on foam surface; eyes closed
- Stand on one leg (right and left)4
- Stance on incline surface, eyes closed
Postural responses 2
Dynamic gait 3
- Compensatory stepping correction; forward
- Change in gait speed
- Compensatory stepping correction; backward
- Walk with head turns; horizontal
- Compensatory stepping correction; lateral (right and left)4
- Walk with pivot turns
- Step over obstacles
- Timed up & go with dual-task
To investigate inter-rater reproducibility, two physical therapists with different experiences of the Mini-BESTest administered and rated the test performance on the same day at Karolinska University Hospital, Stockholm. The more-experienced rater (rater A) had administered and rated the Mini-BESTest more than 100 times, whereas the less-experienced rater (rater B) had administered the test approximately ten times before this study started. To synchronize their assessment of the Mini-BESTest, the two raters met prior to the study on two occasions to discuss the principles of the test, and to practice its administration and rating. However, during and after the test sessions the raters were blinded to each other’s ratings.
Participants were briefly interviewed, using a standardized protocol, regarding current health status including years since diagnosis. Disease severity was measured with the Unified Parkinson’s Disease Rating Scale (UPDRS) , and cognitive function was assessed with the MMSE . Subsequently, the participants performed the Mini-BESTest with each of the two test administrators, who were situated in separate rooms. Randomization decided which administrator to start with. The test procedure took approximately one hour to complete.
For test-retest reproducibility, the more experienced rater (rater A) reassessed the participants seven days later. At the second test session, rater A performed a brief interview, including questions regarding pain, medication, activity, falls, and other possible incidents that might have influenced their balance performance since the previous session. Following this, the participants performed the Mini-BESTest at the same location and time of the day as they had performed the test the previous week.
Statistical analyses were performed with SPSS (version 22, SPSS Inc., Chicago, IL). Cronbach’s alpha was used to assess the internal consistency, where values of at least 0.7 were considered acceptable . Reliability was investigated by means of ICC2.1 where one-way repeated measures analysis of variance (ANOVA) were used to calculate agreement between raters (inter-rater reproducibility) and test sessions (test-retest reproducibility), regarding the total score of the Mini-BESTest as well as its subcomponents. To categorize the level of ICC agreement, we used Altman’s classification: < 0.20 = poor; 0.21–0.40 = fair, 0.41–0.60 = moderate, 0.61–0.80 = good, 0.81–1.0 = very good .
For parameters of agreement, first SEMagreement was calculated as follows: SEM = √within subject error variance . Following this, the SRD was calculated with a 95% Confidence Interval (CI), resulting in the following formula: SRD = 1.96 × √2 × SEM . Moreover, to evaluate the proportion of the measurement error, we calculated the SRD% by dividing the SRD with the maximal total score of the Mini-BESTest (28 points). Similarly, the SRD of each subcomponent was divided with its maximal total score (6 or 10 points). To analyze systematic changes of the mean between testers and test sessions, we used Bland-Altman plots .
All participants completed both test sessions. None of the participants changed their PD medication between the test sessions, nor did they report that any forms of adverse events or change of health status had occurred.
Inter-rater and test-retest reproducibility of the Mini-BESTest and its subcomponents
Mini-BESTest, total score
Anticipatory postural adjustments
Mini-BESTest, total score
Anticipatory postural adjustments
The participants’ mean total score of the Mini-BESTest was found to be 20.2 points for test session one and 20.5 for test session two (Table 3). The Mini-BESTest showed good reliability (ICC = 0.80) and acceptable internal consistency (Cronbach’s alpha = 0.88). Our findings on agreement showed a measurement error of 3.4 points (12% of the maximal total score). The Bland-Altman graph (Figure 1B) showed that, apart from one outlier, no heteroscedasticity was observed. Regarding the agreement of the Mini-BESTest’s subcomponents, we found the measurement error to be highest for the postural responses (27% of the maximal subcomponent score). Conversely, the measurement error was lowest for sensory orientation (13% of the maximal subcomponent score).
This is the first study to use a methodology similar to clinical practice to investigate the reproducibility of the Mini-BESTest, as well as its subcomponents, in PD. We found good reliability  (ICC > 0.70), as well as acceptable internal consistency  (Cronbach’s alpha = 0.87 and 0.88, respectively), for both inter-rater and test-retest reproducibility. However, the agreement was considered low  with the measurement error accounting for, respectively, 15% (4.1 points) and 12% (3.4 points) of the maximal total score.
Seemingly, the reliability of both inter-rater and test-retest reproducibility in this study was good. Nevertheless, these results may seem low compared to prior studies of the Mini-BESTest, with inter-rater ICC scores ranging from 0.91 to 0.99 ,,, and where test-retest scores have ranged from 0.88 to 0.97 ,,,. However, it is difficult to compare directly our results on inter-rater reproducibility with previous studies because either our methodology (with two independent raters) or the participants differs. Indeed, whereas our methodology is comparable to the study of Tsang et al.,  they investigated individuals with chronic stroke. Considering the prevalence of fluctuations of both motor  and non-motor  symptoms in PD, this makes a direct comparison rather faulty. Leddy et al.  on the other hand, studying exclusively elderly with PD, used only one person to administrate the test, whereas three observers rated the test performance. We consider this to be a method that tests the reproducibility of the rating scale of the Mini-BESTest, rather than its reproducibility from a clinical perspective. Moreover, because ICC values are influenced by variability , it is possible that the reasonably low degree of variability in this study (including only participants at Hoehn & Yahr stages 2 and 3, and with the range of Mini-BESTest scores accounting for approximately 40% of the total test score) affected the ICC values negatively.
Hitherto, no previous studies have reported the inter-rater or test-retest agreement of the Mini-BESTest in PD. However, in individuals with mild-to-moderate stroke, Tsang et al.  found the measurement error to be 3 points (11% of the maximal total score) with a test-retest design, which was similar to what we found. Moreover, our results of test-retest agreement are also comparable to those found by Steffen et al.  on the Bergs balance scale in PD. Whereas they found the measurement error to be 5 points out of 56 (9% of the maximal test score), our results of 3.4 points out of 28 (12% of the maximal test score) are just slightly higher. Seemingly, the aforementioned studies (well-designed by appearance and performed in different contexts), similar to ours, have found the measurement error to account for approximately 10% of the total score. Measurement errors of that size, requiring changes of a magnitude that is rare to achieve -, are bound to make it difficult for clinicians to rely on their results with confidence (thereby limiting the instruments clinical value). However, it might be relevant to highlight that these results have been calculated with the prevailing and rather strict formula containing 95% confidence , (meaning that one can be 95% certain that the results are correct). One might consider if it could be of higher clinical value to calculate the measurement error with 80-90% confidence instead , something likely to result in a more manageable measurement error that can be relied upon with 80-90% certainty.
The analysis of the subcomponents of the Mini-BESTest showed that sensory orientation (consisting of only stationary exercises) had the highest agreement, both regarding inter-rater and test-retest reproducibility. Accordingly, the more dynamic subcomponent of postural responses had the lowest agreement. These results were in accordance with those found by Tsang et al. , where items associated with postural responses showed the lowest agreement. This is not surprising because the reactive postural responses subcomponent includes asking persons, possibly frightened of falling, to lean their bodyweight into the hands of the test administrator, who also needs to be consistent regarding how far to lean the persons before suddenly releasing the support. Such a task seems likely to be more challenging than simply to assess the time a person is able to stand on a foam surface with his or her eyes closed. One might argue that these kinds of challenging, nevertheless important, items may be likely to require skilled and well-trained raters.
At inter-rater reproducibility, a systematic bias occurred between the raters, revealing the less experienced rater to score the subjects higher (Figure 1). However, the difference in results between raters (SRD = 4.1) was only marginally larger than between a single rater at two separate occasions (SRD = 3.4). This may indicate that both administrators had a similar understanding of how to administer the test, and that it is quite user-friendly regardless of experience. On the other hand, it might also have been due to the two training occasions that had taken place prior to the data sampling, which in case may emphasize the importance of the preparations before using a test, whether for research purposes or clinical practice. In addition, the results also indicate that the Mini-BESTest consists of items that are difficult, yet important, to assess consistently in elderly with mild-to-moderate PD. Nevertheless, our results suggest that the Mini-BESTest is better suited to distinguish between individuals, rather than to achieve high agreement between test occasions in this population. Future studies, preferably on a more heterogeneous sample, need to investigate whether this may be due to the fluctuations of symptoms in PD , (something that might make this population difficult to assess reliably) or whether measures can be taken to increase the agreement of the Mini-BESTest (such as clearer instructions and increments).
This study has several limitations. First of all, our participants can be considered as a convenience sample, representing only elderly with mild-to-moderate PD who were interested in participating in a balance intervention, therefore our findings can be generalized only to this specific population. In addition, because the total Mini-BESTest scores in this study ranged from 15 to 25 points, we have investigated only this particular interval of the test. Although most training interventions in research ,,, as well as in the clinic, tend to address individuals at the mild-to-moderate stage of the disease, clinical practice also includes treating individuals at more advanced stages of the disease. Moreover, our methodology of using raters with different experience was (although relevant with regard to clinical practice) rather strict- hence it is possible that the results would have been different if both raters had had similar experience. Furthermore, it is possible that the less-experienced test administrator experienced a learning effect during the course of data collection, a form of bias that also might have occurred with the participants as well as with the experienced test administrator at the test-retest assessments (that occurred 7 days after the initial assessments). However, we found no signs of this in our data.
The importance for clinicians to be aware of the agreement of any clinical tool cannot be overestimated. Given the subjective aspects of any test, which include giving instructions and rating performance in general, it is important to know to what extent the outcome may depend upon a measurement error rather than on the actual test performance. This is even more critical in such a demanding task as evaluating an individual’s balance performance, particularly when considering its complex nature. Given the fall-prone nature of a population such as those with PD, where balance problems are all too frequent, this may be of particular value.
Some of the major challenges in obtaining reliable results from many balance tests lie in giving the patients clear and concise instructions while simultaneously ensuring that they will not fall and, at the same time, acknowledging their test performance with an adequate rating. This study has added important information regarding the reproducibility of the Mini-BESTest in elderly with mild-to-moderate PD assessed with a methodology assimilating clinical practice. As we investigated the SRD, these results can be used to evaluate individual treatment. Moreover, these results can also be applied to a group level, (by dividing the SRD found here, with the squared root of the number of participants investigated) . Furthermore, this study also highlighted which subcomponents of the Mini-BESTest were the most difficult to assess consistently, indicating what aspects of the Mini-BESTest test might be beneficial to practice extra carefully prior to balance assessments in those with PD. Moreover, these results may also serve as an indicator of which subcomponents may need to be refined with regard to instructions to the patient as well as further clarifications of how the rating ought to be performed, in order to limit the subjective character of the test to as large an extent as possible. With such measures, we believe that there is great potential to enhance the clinical utility of such a promising test as the Mini-BESTest.
The Mini-BESTest showed good inter-rater and test-retest reproducibility regarding reliability. However, regarding agreement, the measurement error was considered high, with postural responses being the subcomponent with the lowest agreement. This indicates that the Mini-BESTest is able to distinguish between individuals with mild to moderate PD; however, when used in clinical balance assessments, the large measurement error needs to be accounted for.
The authors would like to thank Lisbet Broman for assistance with maneuvering the statistical software program (SPSS). This work was supported by the Swedish Research Council, the Karolinska Institutet, the Gun and Bertil Stohnes Foundation, NEURO Sweden, and the Swedish Parkinson Foundation.
- Dorsey ER, Constantinescu R, Thompson JP, Biglan KM, Holloway RG, Kieburtz K, Marshall FJ, Ravina BM, Schifitto G, Siderowf A, Tanner CM: Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030. Neurol. 2007, 68: 384-386. 10.1212/01.wnl.0000247740.47667.03.View ArticleGoogle Scholar
- Lökk J, Borg S, Svensson J, Persson U, Ljunggren G: Drug and treatment costs in Parkinson's disease patients in Sweden. Acta Neurol Scand. 2012, 125: 142-147. 10.1111/j.1600-0404.2011.01517.x.View ArticlePubMedGoogle Scholar
- Van Den Eeden SK, Tanner CM, Bernstein AL, Fross RD, Leimpeter A, Bloch DA, Nelson LM: Incidence of Parkinson's disease: variation by age, gender, and race/ethnicity. Am J Epidemiol. 2003, 157: 1015-1022. 10.1093/aje/kwg068.View ArticlePubMedGoogle Scholar
- Kim SD, Allen NE, Canning CG, Fung VS: Postural instability in patients with Parkinson's disease. Epidemiology, pathophysiology and management. CNS Drugs. 2013, 27: 97-112. 10.1007/s40263-012-0012-3.View ArticlePubMedGoogle Scholar
- Jankovic J, McDermott M, Carter J, Gauthier S, Goetz C, Golbe L, Huber S, Koller W, Olanow C, Shoulson I, Stern M, Tanner C, Weiner W, the Parkinson Study Group: Variable expression of Parkinson's disease: a base-line analysis of the DATATOP cohort. The Parkinson Study Group. Neurology. 1990, 40: 1529-1534. 10.1212/WNL.40.10.1529.View ArticlePubMedGoogle Scholar
- Schrag A, Jahanshahi M, Quinn N: What contributes to quality of life in patients with Parkinson's disease?. J Neurol Neurosurg Psychiatry. 2000, 69: 308-312. 10.1136/jnnp.69.3.308.View ArticlePubMedPubMed CentralGoogle Scholar
- Franzén E, Paquette C, Gurfinkel V, Horak F: Light and heavy touch reduces postural sway and modifies axial tone in Parkinson's disease. Neurorehabil Neural Repair. 2012, 26: 1007-1014. 10.1177/1545968312437942.View ArticlePubMedPubMed CentralGoogle Scholar
- Horak FB, Wrisley DM, Frank J: The balance evaluation systems test (BESTest) to differentiate balance deficits. Phys Ther. 2009, 89: 484-498. 10.2522/ptj.20080071.View ArticlePubMedPubMed CentralGoogle Scholar
- Franchignoni F, Horak F, Godi M, Nardone A, Giordano A: Using psychometric techniques to improve the balance evaluation systems test: the mini-BESTest. J Rehabil Med. 2010, 42: 323-331. 10.2340/16501977-0537.View ArticlePubMedPubMed CentralGoogle Scholar
- King LA, Priest KC, Salarian A, Pierce D, Horak FB: Comparing the mini-BESTest with the berg balance scale to evaluate balance disorders in Parkinson's disease. Parkinsons Dis. 2012, 2012: 375419-PubMedGoogle Scholar
- de Vet HC, Terwee CB, Knol DL, Bouter LM: When to use agreement versus reliability measures. J Clin Epidemiol. 2006, 59: 1033-1039. 10.1016/j.jclinepi.2005.10.015.View ArticlePubMedGoogle Scholar
- Stratford P: Reliability: consistency or differentiating among subjects?. Phys Ther. 1989, 69: 299-300.PubMedGoogle Scholar
- Weir JP: Quantifying test-retest reliability using the intraclass correlation coefficient and the SEM. J Strength Cond Res National Strength Cond Assoc. 2005, 19: 231-240.Google Scholar
- Leddy AL, Crowner BE, Earhart GM: Utility of the Mini-BESTest, BESTest, and BESTest sections for balance assessments in individuals with Parkinson disease. J Neurol Physical Therapy JNPT. 2011, 35: 90-97. 10.1097/NPT.0b013e31821a620c.View ArticleGoogle Scholar
- Padgett PK, Jacobs JV, Kasser SL: Is the BESTest at its best? A suggested brief version based on interrater reliability, validity, internal consistency, and theoretical construct. Phys Ther. 2012, 92: 1197-1207. 10.2522/ptj.20120056.View ArticlePubMedGoogle Scholar
- Leddy AL, Crowner BE, Earhart GM: Functional gait assessment and balance evaluation system test: reliability, validity, sensitivity, and specificity for identifying individuals with Parkinson disease who fall. Phys Ther. 2011, 91: 102-113. 10.2522/ptj.20100113.View ArticlePubMedPubMed CentralGoogle Scholar
- Jonsdottir J, Cattaneo D: Reliability and validity of the dynamic gait index in persons with chronic stroke. Arch Phys Med Rehabil. 2007, 88: 1410-1415. 10.1016/j.apmr.2007.08.109.View ArticlePubMedGoogle Scholar
- Godi M, Franchignoni F, Caligari M, Giordano A, Turcato AM, Nardone A: Comparison of reliability, validity, and responsiveness of the mini-BESTest and Berg Balance Scale in patients with balance disorders. Phys Ther. 2013, 93: 158-167. 10.2522/ptj.20120171.View ArticlePubMedGoogle Scholar
- Wong CK: Interrater reliability of the Berg Balance Scale when used by clinicians of various experience levels to assess people with lower limb amputations. Phys Ther. 2014, 94: 371-378. 10.2522/ptj.20130182.View ArticlePubMedGoogle Scholar
- Faria CD, Teixeira-Salmela LF, Nadeau S: Clinical testing of an innovative tool for the assessment of biomechanical strategies: the Timed "Up and Go" Assessment of Biomechanical Strategies (TUG-ABS) for individuals with stroke. J Rehabil Med. 2013, 45: 241-247. 10.2340/16501977-1106.View ArticlePubMedGoogle Scholar
- McConvey J, Bennett SE: Reliability of the dynamic gait index in individuals with multiple sclerosis. Arch Phys Med Rehabil. 2005, 86: 130-133. 10.1016/j.apmr.2003.11.033.View ArticlePubMedGoogle Scholar
- Tsang CS, Liao LR, Chung RC, Pang MY: Psychometric properties of the mini-balance evaluation systems test (mini-BESTest) in community-dwelling individuals with chronic stroke. Phys Ther. 2013, 93: 1102-1115. 10.2522/ptj.20120454.View ArticlePubMedGoogle Scholar
- Looney MA: When Is the Intraclass Correlation Coefficient Misleading?. Meas Phys Educ Exerc Sci. 2000, 4: 73-78. 10.1207/S15327841Mpee0402_3.View ArticleGoogle Scholar
- Beckerman H, Roebroeck ME, Lankhorst GJ, Becher JG, Bezemer PD, Verbeek AL: Smallest real difference, a link between reproducibility and responsiveness. Q Life Res. 2001, 10: 571-578. 10.1023/A:1013138911638.View ArticleGoogle Scholar
- Conradsson D, Löfgren N, Ståhle A, Hagströmer M, Franzén E: A novel conceptual framework for balance training in Parkinson's disease-study protocol for a randomised controlled trial. BMC Neurol. 2012, 12: 111-10.1186/1471-2377-12-111.View ArticlePubMedPubMed CentralGoogle Scholar
- Hughes AJ, Daniel SE, Kilford L, Lees AJ: Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry. 1992, 55: 181-184. 10.1136/jnnp.55.3.181.View ArticlePubMedPubMed CentralGoogle Scholar
- Folstein MF, Folstein SE, McHugh PR: "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975, 12: 189-198. 10.1016/0022-3956(75)90026-6.View ArticlePubMedGoogle Scholar
- King L, Horak F: On the mini-BESTest: scoring and the reporting of total scores. Phys Ther. 2013, 93: 571-575. 10.2522/ptj.2013.93.4.571.View ArticlePubMedGoogle Scholar
- Movement Disorder Society Task Force on Rating Scales for Parkinson's D: The unified Parkinson's disease rating scale (UPDRS): status and recommendations. Move Disord Off J Move Disord Soc. 2003, 18: 738-750. 10.1002/mds.10473.View ArticleGoogle Scholar
- Cronbach LJ, Warrington WG: Time-limit tests: estimating their reliability and degree of speeding. Psychometrika. 1951, 16: 167-188. 10.1007/BF02289113.View ArticlePubMedGoogle Scholar
- Altman DG: Practical statistics for medical research. 1991, Chapman & Hall/CRC, LondonGoogle Scholar
- Terwee CB, Bot SD, de Boer MR, van der Windt DA, Knol DL, Dekker J, Bouter LM, de Vet HC: Quality criteria were proposed for measurement properties of health status questionnaires. J Clin Epidemiol. 2007, 60: 34-42. 10.1016/j.jclinepi.2006.03.012.View ArticlePubMedGoogle Scholar
- Bland JM, Altman DG: Statistical methods for assessing agreement between two methods of clinical measurement. Lancet. 1986, 1: 307-310. 10.1016/S0140-6736(86)90837-8.View ArticlePubMedGoogle Scholar
- Smidt N, van der Windt DA, Assendelft WJ, Mourits AJ, Deville WL, de Winter AF, Bouter LM: Interobserver reproducibility of the assessment of severity of complaints, grip strength, and pressure pain threshold in patients with lateral epicondylitis. Arch Phys Med Rehabil. 2002, 83: 1145-1150. 10.1053/apmr.2002.33728.View ArticlePubMedGoogle Scholar
- Ahlskog JE, Muenter MD: Frequency of levodopa-related dyskinesias and motor fluctuations as estimated from the cumulative literature. Move Disord. 2001, 16: 448-458. 10.1002/mds.1090.View ArticleGoogle Scholar
- Storch A, Schneider CB, Wolz M, Sturwald Y, Nebe A, Odin P, Mahler A, Fuchs G, Jost WH, Chaudhuri KR, Koch R, Reichmann H, Ebersbach G: Nonmotor fluctuations in Parkinson disease: severity and correlation with motor complications. Neurology. 2013, 80: 800-809. 10.1212/WNL.0b013e318285c0ed.View ArticlePubMedGoogle Scholar
- Steffen T, Seney M: Test-retest reliability and minimal detectable change on balance and ambulation tests, the 36-item short-form health survey, and the unified Parkinson disease rating scale in people with parkinsonism. Phys Ther. 2008, 88: 733-746. 10.2522/ptj.20070214.View ArticlePubMedGoogle Scholar
- Smania N, Corato E, Tinazzi M, Stanzani C, Fiaschi A, Girardi P, Gandolfi M: Effect of balance training on postural instability in patients with idiopathic Parkinson's disease. Neurorehabil Neural Repair. 2010, 24: 826-834. 10.1177/1545968310376057.View ArticlePubMedGoogle Scholar
- Tarakci E, Yeldan I, Huseyinsinoglu BE, Zenginler Y, Eraksoy M: Group exercise training for balance, functional status, spasticity, fatigue and quality of life in multiple sclerosis: a randomized controlled trial. Clin Rehabil. 2013, 27: 813-822. 10.1177/0269215513481047.View ArticlePubMedGoogle Scholar
- Harro CC, Shoemaker MJ, Frey OJ, Gamble AC, Harring KB, Karl KL, McDonald JD, Murray CJ, Tomassi EM, Van Dyke JM, VanHaistma RJ: The effects of speed-dependent treadmill training and rhythmic auditory-cued overground walking on gait function and fall risk in individuals with idiopathic Parkinson's disease: a randomized controlled trial. NeuroRehabilitation. 2014, 34: 557-572.PubMedGoogle Scholar
- Tveter AT, Dagfinrud H, Moseng T, Holm I: Measuring health-related physical fitness in physiotherapy practice: reliability, validity, and feasibility of clinical field tests and a patient-reported measure. J Orthop Sports Physical Ther. 2014, 44: 206-216. 10.2519/jospt.2014.5042.View ArticleGoogle Scholar
- Frazzitta G, Pezzoli G, Bertotti G, Maestri R: Asymmetry and freezing of gait in parkinsonian patients. J Neurol. 2013, 260: 71-76. 10.1007/s00415-012-6585-4.View ArticlePubMedGoogle Scholar
- Yogev-Seligmann G, Giladi N, Brozgol M, Hausdorff JM: A training program to improve gait while dual tasking in patients with Parkinson's disease: a pilot study. Arch Phys Med Rehabil. 2012, 93: 176-181. 10.1016/j.apmr.2011.06.005.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.