Development and validation of a novel questionnaire for self-determination of the range of motion of wrist and elbow
© The Author(s). 2016
Received: 7 April 2016
Accepted: 8 July 2016
Published: 26 July 2016
The aim of this study was to develop and validate a novel self-administered questionnaire for assessing the patient’s own range of motion (ROM) of the wrist and the elbow.
In a prospective clinical study from January 2015 to June 2015, 101 consecutive patients were evaluated with a novel, self-administered, diagram-based, wrist motion assessment score (W-MAS) and elbow motion assessment score (E-MAS). The questionnaire was statistically evaluated for test-retest reliability, patient-physician agreement, comparison with healthy population, and influence of covariates (age, gender, affected side and involvement in workers’ compensation cases).
Assessment of patient-physician agreement demonstrated almost perfect agreement (k > 0.80) with regard to six out of eight items. There was substantial agreement with regard to two items: elbow extension (k = 0.76) and pronation (k = 0.75). The assessment of the test-retest reliability revealed at least substantial agreement (k = 0.70). The questionnaire revealed a high discriminative power when comparing the healthy population with the study group (p = 0.007 or lower for every item). Age, gender, affected side and involvement in workers’ compensation cases did not in general significantly influence the patient-physician agreement for the questionnaire.
The W-MAS and E-MAS are valid and reliable self-administered questionnaires that provide a high level of patient-physician agreement for the assessments of wrist and elbow ROM.
Level of evidence: Diagnostic study, Level II
KeywordsSelf-assessment Measurement tool Validity Reliability Range of motion Wrist Elbow Questionnaire
Assessing the patient’s outcome and satisfaction is important in modern orthopedic practice [1–3]. Using questionnaires to evaluate patients with wrist and elbow disorders is widespread and has been shown to be valid and reproducible [4–9]. Self-reported outcome measures allow outcomes to be assessed from the patient’s perspective and do not require time in clinic or medical staff for data collection.
Common self-administered questionnaires for the determination of hand- and upper limp specific results of the wrist (e.g. patient-rated wrist evaluation, PRWE ) and of the elbow (e.g. The American Shoulder and Elbow Surgeons-Elbow, ASES-E ) enable the patient to assess the functional impairment of the joint, but they do not formally assess the range of motion, and patients have to attend clinic for this to be measured . Therefore important data regarding the ROM would be lost in patients who are unable or unwilling to come to the outpatient clinic at the regular follow-up or for clinical research.
To our knowledge no validated self-assessment questionnaire for the ROM of the wrist or the elbow exists, which compares the agreement of the patient’s outcome with the examination by a physician.
Therefore, the aim of the current study was to develop a self-administered, diagram-based wrist motion assessment score (W-MAS) and elbow motion assessment score (E-MAS) to enable the patients to assess their own ROM of the wrist and the elbow. We further evaluated validity and reliability of this novel questionnaire with respect to the accuracy of self-determination of the wrist and elbow ROM.
In this prospective, single-center study the novel questionnaire was evaluated in patients with elbow or wrist disorders. Before development of this novel questionnaire a PubMed search was performed to identify the currently available self-administered questionnaires for the wrist and elbow joints.
PubMed was searched in May 2016 for elbow- and wrist-specific MeSH-terms (‘elbow’ or ‘wrist’ in combination with ‘scoring system’, ‘outcome assessment’, ‘elbow disorder’, ‘wrist disorder’, ‘questionnaire’, ‘instrument’ and ‘clinical evaluation’), with no limit regarding the year of publication.
Patient-administered questionnaires for the wrist and the elbow
Self-assessment of ROM
Patient-physician validated ROM
Disabilities of the Arm, Shoulder and Hand (DASH)
Beaton et al. 
Patient-Rated Elbow Evaluation (PREE)
MacDermid et al. 
American Shoulder and Elbow Surgeons-Elbow Score (ASES-E)
King et al. 
Broberg and Morrey rating system (BMS)
Broberg et al. 
Elbow Self-Assessment Score (ESAS)
Beirer et al. 
Oxford Elbow Score (OES)
Dawson et al. 
Liverpool Elbow Score (LES)
Sathyamoorthy et al. 
Patient-Rated Tennis Elbow Evaluation Questionnaire (PRTEE)
Vincent et al. 
Ewald scoring system
Khalfayan et al. 
Patient-Rated Wrist Evaluation (PRWE)
MacDermid et al. 
Michigan Hand Outcomes Questionnaire (MHOQ)
Chung et al. 
Musculoskeletal Functional Assessment (MFA)
Engelberg et al. 
Modern Activity Subjective Survey of 2007 (MASS07)
Alexander et al. 
Levine Questionnaire (LQ)
Levine et al. 
Mayo Wrist Score
Cooney et al. 
Cooney and Bussey Score
Cooney et al. 
Munich Wrist Questionnaire
Beirer et al. 
The extension and flexion of the elbow and the radial and ulnar deviation of the wrist were imaged with increments of 10°. Forearm supination and pronation as well as the extension and flexion of the wrist were imaged with an increment of 20°. These increments have been chosen to improve reproducibility without loss of information. For the assessment of the ROM, photographs were taken of a volunteer with an unimpaired wrist and elbow function. The joint position was measured and the volunteer was asked to hold the position briefly for the photograph. Additionally, the correct joint angle was then controlled with an electronic measurement device of Microsoft Word™ to ensure an accurate joint position on each image (Additional file 1: E-MAS, Additional file 2: W-MAS).
Finally, the E-MAS consists of 15 images for the extension (seven items, E-Ext) and flexion (eight items, E-Flex) of the elbow and ten images for supination (six items, Sup) and pronation (five items, Pro) of the forearm. The W-MAS consists of nine images addressing the extension (five items, W-Ext) and flexion (four items, W-Flex) of the wrist and six images addressing the radial- (three items, Rad) and ulnar deviation (four items, Uln).
Supination and pronation was performed with 90° of elbow flexion and the upper arm adjacent to the torso. To standardize forearm supination and pronation without rotation of the shoulder a short instructive direction was set in front of the related images. The objectivity of application and data interpretation (content validity) is guaranteed by the questionnaire-format with a clear answer form (possible-not possible) [11, 12].
Prior to a physical examination, the patient was asked to fill out the questionnaire. According to the directions on the questionnaire, patients were asked to check whether they are able to achieve the movements on each photograph for the wrist and the elbow on both sides. After completion of the questionnaire, the actual elbow and wrist ROM of both sides was measured by a single examiner [MS] using a standard 12-inch goniometer, regardless of whether the wrist and/or the elbow were the affected joint. The examiner was blinded to the self-reported ROM.
For assessment of the test-retest reliability the questionnaire was sent to the patients after an average of 65 (SD 21) days after the visit to clinic to prevent recall bias. Additionally, the patients were asked if there had been a change in the motion of any involved joint, and they were excluded from the assessment of test re-test-reliability in the case of a positive answer.
Between January 2015 and July 2015, 101 consecutive patients suffering from disorders of the wrist and/or elbow were recruited at our outpatient clinic for participation in this study. These patients were identified from a consecutive list of patients scheduled for a follow-up visit as a prospective cohort. The inclusion criteria were age over 18 and disorder of the wrist and/or the elbow on one side. A subset of 58 patients (those, who denied having an altered ROM at the time of re-test) was re-assessed for evaluating the test-retest reliability.
Another 30 healthy people were recruited as a control group to test if the questionnaire can distinguish between patients with and without disorders of the wrist or elbow. The inclusion criteria for the control group were age over 18 and unimpaired function of the upper extremity. Exclusion criteria for control group and the study group were cognitive diseases, psychiatric diseases, communication problems or dyslexia.
Descriptive statistics (mean, standard deviation, median, interquartile range, absolute and relative frequencies) were calculated to characterize the study population. The W-MAS and E-MAS were validated according to the proposed quality criteria for measurement properties of health status questionnaires of Terwee et al. . The statistical evaluation included the assessment of (1) test–retest reliability, (2) agreement analysis (criterion validity and construct validity with Spearman correlation of at least 0.7), (3) comparison with healthy population (responsiveness) and (4) influence of covariates (age, gender, affected side and involvement in workers’ compensation cases). Floor and ceiling effects and interpretability were considered to be not relevant for the validation of these questionnaires as no mean score can be achieved.
The self-assessments by patients and the assessments by physicians are both represented by ordinal variables (ROM categorized into 4 to 8 groups). In the case of a missing item, only this specific motion pattern could not be evaluated.
The test-retest reliability defines the degree of agreement of repeated measurements in the same subjects measured to assess the repeatability and reproducibility of an instrument. The time period between the measurements should be long enough to avoid learning and memory effects, but at the same time short enough to ensure consistency of the clinical symptoms . Our target was to perform retests 2 months after baseline assessment. According to literature the time interval should be at least 2 weeks to prevent recall bias .
Reliability between the repeated measurements was assessed using Spearman’s rank correlation and Kendall’s Tau b correlation coefficient. To assess the agreement, Cohen’s kappa and the probability of exact agreement (number of test-retest agreements/n, expressed as percentage) were derived.
An agreement analysis assesses the extent to which a new instrument relates to the true value or to a gold standard value. In the context of assessing the ROM, industrial robotic devices and optical motion analysis can be considered as the gold standard [13, 14]. For practical reasons physician ratings were chosen as the reference in the current study. The Spearman rank correlation was used to evaluate the relation between patients’ and physicians’ response. A positive rating for the agreement analysis was assumed when the Spearman correlation was at least 0.7 . To assess the agreement, the probability of exact and approximate agreement (expressed as percentage) and Cohen’s kappa were calculated.
Classification of three subgroups of severity of disorder for every item of the E-MAS and the W-MAS
Elbow (in degrees)
Wrist (in degrees)
Exact agreement was defined as those cases in which physician and patient chose an identical response. Approximate agreement was defined as agreement within one grade, in a positive or negative direction.
Comparison with healthy population
To assess the extent to which the questionnaires could distinguish healthy persons from persons with wrist or elbow disorder, Mann-Whitney U-tests were performed to compare the scoring.
Influence of covariates
The influence of age (in decades), gender, affected side (dominant or non-dominant upper limb) and involvement in workers’ compensation cases on the patient-physician agreement was analyzed using univariable logistic regression.
For agreement measures of categorical data, the benchmarks as described by Landis and Koch where used: 0.00 to 0.20, 0.21 to 0.40, 0.41 to 0.60, 0.61 to 0.80, and 0.81 to 1.00 indicate poor, fair, moderate, substantial, and almost perfect agreement, respectively . The agreement should be at least 0.70 to be adequate .
Benchmarks for the Spearman rank correlation are not consistent in the literature. We used 0.00 to 0.20, 0.21 to 0.50, 0.51 to 0.80, and 0.81 to 1.0 indicating no, weak, moderate, and strong relationship, respectively.
A p-value < 0.05 is considered as statistically significant in a descriptive manner. Statistical analysis was performed using SPSS (version 21.0 for Windows).
Distribution of injury pattern
No. patients (%)
Complex elbow dislocation
Radial head fracture
Distal radius fracture
Simple elbow dislocation
Distal humerus fracture
Monteggia like lesion
Humeral shaft fracture
Proximal ulnar fracture
Forearm shaft fracture
Arthritis of the elbow
Osteochondritis dissecans Capitellum humeri
Loose bodies elbow
A subgroup of 58 patients (57.4 %) from the study population was evaluated for test-retest reliability. Mean age of this subgroup was 56.7 years (range 37 to 81, SD 11.7), 31 (53.4 %) were male and 27 (46.6 %) were female. Another 30 healthy participants were recruited as a control group, mean age was 24.9 years (range 20 to 61, SD 11.4), ten (33.3 %) were male and 20 (66.6 %) were female. None of the 131 patients found any of the given instructions difficult to understand or to follow. The questionnaire took a maximum of 5 min for patients to complete.
Statistics for test-retest reliability for the different parts of the questionnaire, n = 58
n = 58
Kendall-Tau-b (95 %-CI)
Spearman’s rank correlation coefficient (95 %-CI)
Cohen’s kappa (95 %-CI)
Exact agreement (in %)
Statistics for patient-physician agreement for the different parts of the questionnaire, n = 101
n = 101
Kendall-Tau-b (95 %-CI)
Spearman’s rank correlation coefficient (95 %-CI)
Cohen’s kappa (95 %-CI)
Exact agreement (in %)
In the case of disagreement between the physician and patient responses, patients tended to err toward underestimating their ROM, meaning that the patient rated the ROM worse than the physician did. In 2–12.9 % patients tended to err towards underestimating their ROM and in 1 to 5 % patients tended to err towards overestimating their ROM.
Comparison with healthy population
Comparison of study population with healthy population for discriminative power for the different parts of the questionnaire
Elbow disorder (n = 79)
Healthy population (n = 30)
Elbow; median (IQR) [in degree]
Wrist disorder (n = 22)
Healthy population (n = 30)
Wrist; median (IQR) [in degree]
Influence of basic demographic data
Logistic regression analysis showed a significant effect of age on the ability to accurately assess elbow extension (p = 0.034). Younger patients were reliably able to identify elbow extension using the questionnaire, whereas elderly patients made significantly more errors. In all other items age did not affect the ability to achieve exact agreement with the questionnaire (p >0.05) and the OR was between 0.639 and 1.254.
No statistically significant association between ability to accurately assess wrist or elbow ROM and gender (p >0.05) or involvement of the dominant side (p >0.05) was observed.
Involvement with workers’ compensation cases significantly affected the ability to accurately assess the pronation (p = 0.039). All other items were not significantly influenced by the involvement with workers’ compensation (p >0.05).
Detailed analyses demonstrated that patients who were involved in workers’ compensation cases (n = 42, 41.6 %) tended to err towards underestimating their ROM in 27 of 43 cases (62.8 %).
In the present study the development and validation of a novel self-administered questionnaire for assessing the patient’s own range of motion of the wrist (W-MAS) and the elbow (E-MAS) are described. This study revealed substantial to almost perfect patient-physician agreement for the self-assessment of the wrist and elbow ROM. Evaluation of patient-physician correlation demonstrated almost perfect agreement (k >0.80) with regard to six of the eight items and two items (elbow extension and pronation) showed substantial agreement with k >0.70. In the case of mismatch between patient and physician, patients tended to err towards underestimating their ROM (53 of 78 cases; 68.9 %). In case of severe restriction of ROM patients tended to miss exact agreement in 23.5 to 50 % in five of eight items.
The assessment of the test–retest reliability was found to be almost perfect with Cohen’s kappa of k > 0.80 for all eight items. The questionnaire revealed a high discriminative power when the healthy population was compared with the study group (p = 0.007 or smaller for all items).
Logistic regression analysis suggested that increasing age impairs the ability to accurately assess elbow extension (p = 0.034). Involvement with workers’ compensation cases also appeared to influence the ability to accurately assess the pronation (p = 0.039).
For all other items, age and involvement in workers’ compensation cases did not significantly influence the validity of the questionnaire. Gender (male vs. female) and affected side (dominant vs. non-dominant) did also not significantly influence the validity of the questionnaire. The W-MAS and the E-MAS are the first questionnaires to validate the patient-physician agreement for ROM of the wrist and the elbow. According to the proposed quality criteria for measurement properties of health status questionnaires of Terwee et al. both questionnaires, the W-MAS and E-MAS are fully validated .
Smith et al. and Carter et al. examined the agreement between physician and patient-derived values for the shoulder ROM. They concluded, that patients are able to accurately assess their own active shoulder ROM with the help of a diagram-based questionnaire, which is comparable to the results of the current study [10, 18].
Given the number of available wrist and elbow questionnaires, is there a need for a novel self-administered score of the elbow and the wrist? In current medical care, self-administered questionnaires are useful for the assessment of patient care and for recording outcomes in research [2, 19]. Physicians can benefit from mail-in questionnaires or internet-based reporting sites and they can use such a tool to track a patient’s objective progress over time. In the same way, once a patient has been formally discharged from regular care, patient-administered questionnaires can be completed and returned via the postal service, e-mail, self-reporting website or even a smartphone app. This approach can facilitate long-term follow-up of postoperative patients for clinical trials by use of the objective criterion, ROM. According to our literature search, most available self-administered questionnaires for the wrist and the elbow do not assess ROM. Three questionnaires were identified with self-assessment of ROM, but these were not validated for patient-physician agreement. Therefore, important data regarding the ROM would be lost in patients who are unable or unwilling to come to the outpatient clinic at the regular follow-up.
Another possible advantage of self-administered questionnaires for determining ROM is the fact that the physician’s influence on the data obtained is minimized. Concerns and priorities of the surgeon may differ from those of the patient . On the other hand, self-assessment of objective and subjective criteria may contain some bias . In this study, basic demographic data like age, gender or involvement in workers’ compensation showed (except for 2 items) no significant influence on the validity and reliability of the questionnaire.
Self-administered questionnaires have some limitations. Patient-physician agreement in the assessments of the range of motion depends on the ability of the patient to understand the images given. The motion patterns given in this study are simple compared to other joints like the shoulder. All participants in the study and control group were asked about the feasibility of the questionnaire. None of the patients had any problems following the instructions and completing the questionnaire. In the current study, patients with communication problems or dyslexia were excluded, as they would not be able to provide useful information for the study.
There are certain weaknesses inherent to this study. The assessment of ROM by physician is usually represented by a continuous variable. In the current study, the assessments by physicians and the patients are both represented by ordinal variables due to practicability and comparability. As with any patient-reported outcomes survey, some patients are not able to complete the questionnaire. An inability to complete the questionnaire should alert clinicians that these patients might need to be carefully monitored between office visits or after formally discharge from care. In case of major restriction of ROM a higher percentage of disagreement between the physician and patient was found. Those patients also may require more specialized follow-up in certain settings.
This study is limited by the heterogeneity of the included injury patterns, as the majority of patients had restriction of ROM due to traumatic elbow disorders. Further study may be needed to have this questionnaire generalizable to other elbow and wrist complaints.
This novel, patient-administered questionnaire provides a high level of patient-physician agreement for assessing the range of motion of the wrist (W-MAS) and the elbow (E-MAS). Based on the present data, both questionnaires are quick, simple to answer, and fully validated, and can be a helpful addition to subjective self-assessment questionnaires of the wrist and the elbow. In addition with other self-assessment scores of the upper limb, these questionnaires can provide helpful information regarding ROM of wrist and elbow to obtain higher follow-up rates.
ASES-E, The American Shoulder and Elbow Surgeons-Elbow; DRUJ, distal radioulnar joint; E-Ext, elbow extension; E-Flex, elbow flexion; E-MAS, elbow-motion assessment score; Pro, pronation; PRUJ, proximal radioulnar joint; PRWE, patient-rated wrist evaluation; Rad, radial deviation; ROM, range of motion; Sup, supination; Uln, ulnar deviationW-Ext, wrist extension; W-Flex, wrist flexion; W-MAS, wrist-motion assessment score
We acknowledge the financial support by Deutsche Forschungsgemeinschaft and Ruprecht-Karls-Universität Heidelberg within the funding programme “Open Access Publishing”.
This study is supported by Deutsche Forschungsgemeinschaft and Ruprecht-Karls-Universität Heidelberg within the funding programme “Open Access Publishing”.
Availability of data and materials
Data are available on request from the corresponding author.
MS and TG were involved with the design of the study, statistical analysis and manuscript preparation. SS was involved with the data interpretation, statistical analysis and manuscript preparation. HK, SA, SSF and PAG assisted with the data interpretation and manuscript preparation. All authors read and approved the final manuscript.
TG is senior consultants at the BG Trauma Center Ludwigshafen. PAG is the Medical Director of the BG Trauma Center Ludwigshafen.
The authors declare that they have no competing interests.
Consent for publication
The person that is imaged on the questionnaires gave written informed consent for publication.
Ethics approval and consent to participate
The study was approved by the local ethics committee of the board of Medical Profession of Rhineland-Palatinate in Mainz (No. 837.268.15/10036). Written informed consent was obtained from all patients participating in the study.
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