Abstract
Background:
The Victorian Institute of Sport Assessment-Patella (VISA-P) questionnaire is a widely accepted instrument for measuring the severity of symptoms and pain in patients having sustained patellar tendinopathy.
Purpose:
To adapt the VISA-P questionnaire cross-culturally to a traditional Chinese version (VISA-P-Ch) and validate its psychometric properties.
Study Design:
Cohort study (diagnosis); Level of evidence, 3.
Methods:
The VISA-P questionnaire was adapted to a traditional Chinese version following international recommended guidelines, including translation, synthesis, back translation, revision by expert committee, pretesting, and validation. The psychometric properties were tested in 15 healthy controls and 15 participants with patellar tendinopathy. Face validity was judged by the authors and participants. Known-groups validity was tested by comparing the VISA-P-Ch scores between symptomatic and asymptomatic participants using an independent t test. Concurrent validity was determined by comparing the Blazina classification of the participants against VISA-P-Ch scores using the Spearman correlation coefficient. Test-retest reliability was assessed by calculating the intraclass correlation coefficient (ICC) following a 24- to 48-hour interval. Internal consistency was determined by the Cronbach alpha.
Results:
The expert committee and participants reported good face validity of the VISA-P-Ch. Significantly higher scores were found in the control group than in the patellar tendinopathy group (98.47 ± 3.04 vs 65 ± 11.9; P < .001). Concurrent validity showed a high correlation between VISA-P-Ch and the Blazina classification system (r = -0.899; P < .01). The test-retest reliability was excellent (ICC = 0.964). Internal consistency was found to be good for both the first and second assessments (Cronbach α = 0.834 and 0.851).
Conclusion:
The VISA-P-Ch was proven to be a reliable and valid questionnaire with similar psychometric properties as the original VISA-P.
Keywords: VISA-P-Ch, patellar tendinopathy, reliability, validity
Patellar tendinopathy is the most common overuse injury in sports, especially for sports that require repeated jumping and landing. 15 High demand for knee extensor mechanism during jumping and landing leads to the cumulative repetitive microtraumas of the patellar tendon, which subsequently causes tenderness during sports at the insertion of the patellar tendon.3,10,20,26 Particularly high prevalence of patellar tendinopathy has been found in sports characterized by high demands of leg power and speed, such as volleyball (45%) and basketball (32%). 15
Due to the high prevalence of patellar tendinopathy, early diagnosis and treatment are important for athletes so as to avoid interruption to sports activity and performance. Whereas imaging may assist in the differential diagnosis of other anterior knee pain sources, the poor correlation between ultrasound and clinical symptoms, 14 combined with the high cost and limited accessibility of magnetic resonance imaging (MRI), the diagnosis of patellar tendinopathy remains largely clinical. 6 This highlights the need and importance of a questionnaire-based index of severity to identify relevant symptoms in patients suspected of having patellar tendinopathy.
The Victorian Institute of Sport Assessment-Patella (VISA-P) questionnaire was developed in 1998 and has repeatedly proved reliable in assessing and quantifying severity of patellar tendinopathy. 22 It has also been applied to assess results after treatment. 9 As the only disease-specific scale for patellar tendinopathy, VISA-P is a widely accepted and valid tool for the assessment of patellar tendinopathy, and it has been adapted for Swedish, Italian, Dutch, German, Spanish, Brazilian, Korean, Turkish, French, Greek, Kannada, and simplified Chinese populations in the past few years. ** However, there is currently no traditional Chinese version of the VISA-P (VISA-P-Ch) available for use.
Given the efficacy of the VISA-P in clinical assessment of patellar tendinopathy, we aimed to validate the VISA-P-Ch to broaden the use of this tool for this specific population. We hypothesized that the VISA-P-Ch would be a valid and reliable instrument for the Chinese population specifically.
Methods
The study protocol was approved by our institutional review board, and all participants provided written informed consent. The study participants were administrated the VISA-P-Ch twice within a 24- to 48-hour time interval. All data acquisition and procedures were conducted by the same investigator (F.-Y.S.) to standardize the procedure. The investigator obtained the demographic data from the participants, evaluated the participants according to the Blazina classification system (1, pain only after sports; 2, pain only at the beginning of sports; 3, constant pain at rest and with activity; 4, patellar tendon rupture), and obtained the first score of the VISA-P-Ch. The score of the second evaluation was obtained via return mail from participants. There was no loss to follow-up between the first and second evaluations.
Participants
A total sample of 30 participants was divided into 2 groups according to their self-reported symptoms during functional activities. The patellar tendinopathy group was defined by the presence of pain at the patellar tendon during functional activities such as jumping, squatting, and landing for >3 months in the past year. The participants were classified into the asymptomatic group if they reported to have never been diagnosed with patellar tendinopathy and there was no pain on the anterior part of the knee. Participants who had other conditions, such as lower extremities fracture; a history of surgery; pain in joints other than the knee; or rheumatic, systematic, and neurological diseases, or who could not understand Chinese were excluded.
Description of VISA-P Questionnaire
The VISA-P is scored from 0 to 100, with a lower score indicating more severe symptoms of patellar tendinopathy. There are a total of 8 questions; the score for each of the first 7 items ranges from 0 to 10 points. The eighth question is divided into 3 parts (8a, 8b, and 8c) for different conditions and scores independently. Of the 8 questions, 6 rate the degree of symptoms in daily living and simple functional tests. The remaining 2 questions concern ability in sports participation (Appendix Figure A1).
Translation Procedure
Initial Translation
The forward translation is the initial step for translating the questionnaire from English to traditional Chinese. This step was performed independently by 2 bilingual speakers (Y.-L.L., C.-Y.C.) whose native language is traditional Chinese. Both translators were professors of physical therapy with extensive knowledge of the English language and the context of VISA-P.
Synthesis
After the initial translation, the 2 translators, as well as members of the research team, held a meeting to achieve an initial translation consensus and synthesized a pretesting of the VISA-P-Ch.
Backward Translation
The backward translation was performed independently by 2 native English speakers who were fluent in Chinese. One was a professor of physical therapy and the other was a medical student, and both were blinded to the original VISA-P. (A.C., B.Y.-T.H.)
Expert Committee Meeting
An expert committee consisted of 2 native traditional Chinese speakers and 2 native English speakers (Y.-L.L., C.-Y.C., A.C., B.Y.-T.H.) met to review the traditional Chinese version of the VISA-P and to achieve consensus on each item within the questionnaire; 3 members were professors of physical therapy, while 1 was a medical student. All committee members had comprehensive knowledge of sports orthopaedics.
All the translators and research team then met to consider and discuss all of the versions of the questionnaires until a general consensus was reached to produce a provisional VISA-P-Ch that is semantically, idiomatically, conceptually, and experimentally equivalent to the original VISA-P.
Pretesting
The provisional traditional VISA-P-Ch was administered to 8 asymptomatic participants (3 men and 5 women). After completing the questionnaire, each participant was interviewed regarding linguistic understanding, fluency, and expression relevance to the Chinese culture of each item. The test of the provisional version revealed that the term “full weightbearing” in Chinese was hard to understand, there was no specific term for the word “lunge” in Chinese, and the symbol “±” in the sentence was confusing for participants. Thus, the committee agreed to add an explanation after the word “full weightbearing” in Chinese and an illustration for “lunge” as well as exchange the “±” for “and/or.”
The final version of the VISA-P-Ch was then administered for psychometric evaluation to determine its validity and reliability.
Validity Testing
Face Validity
Face validity was assessed by showing the questionnaire to authors and participants to determine whether they perceived the items to be appropriate and relevant.
Concurrent Validity
Concurrent validity was determined by the correlation between Blazina classification measures and the scores of VISA-P-Ch. The Blazina classification measures the impact of pain in functional activities for patellar tendinopathy, which has been used in the research and development of Greek, German, and Kannada versions of the VISA-P and has been proven to be highly correlated with the VISA-P questionnaire.
Known-Groups Validity
Known-groups validity was assessed by the comparing the VISA-P-Ch scores between symptomatic and asymptomatic groups.
Test-Retest Reliability
The test-retest reliability determines the consistency of an instrument in measuring the performance of a group of subjects over a period. For this analysis, the interval between the 2 evaluations was set to 24 to 48 hours to minimize a change in disease status but long enough to avoid recall of responses.
Internal Consistency
The internal consistency indicates the homogeneity between different items in the same measurement tool that propose to measure the same construct produce similar scores. Internal consistency of the VISA-P-Ch was evaluated by determining the Cronbach alpha coefficient (α).
Statistical Analyses
Differences in demographic data between the patellar tendinopathy group and healthy group were compared using an independent t test. Concurrent validity was established by the Spearman rank correlation between VISA-P-Ch scores and Blazina classification. Known-groups validity was obtained through comparing the VISA-P-Ch score between groups using 1-way analysis of variance. Test-retest reliability was conducted by intraclass correlation coefficient (ICC) to compare VISA-P-Ch scores between the 2 evaluation timepoints. ICC values were interpreted as poor if <0.5, moderate if between 0.5 and 0.75, good if between 0.75 and 0.9, and excellent if >0.9. 12 Internal consistency of the total VISA-P-Ch score was assessed using the Cronbach alpha. Standard error of measurement (SEM) was calculated to indicate the absolute reliability of the measure. The minimal detectable change was calculated to represent the minimum amount of change that can be interpreted as a real change and not attributed simply to measurement error. The level for statistical significance was set at P < .05.
Results
The characteristics of the participants are presented in Table 1. The training frequency was significantly higher in the patellar tendinopathy group (2.81 ± 1.99 vs 11.71 ± 11.03 hours per week; P = .008). The VISA-P-Ch score was 98.5 ± 0.8 for the control group and 65.0 ± 3.1 for participants with patellar tendinopathy.
Table 1.
Characteristics of Participants a
| Patellar Tendinopathy (n = 15) | Control (n = 15) | |
|---|---|---|
| Age, y | 26 ± 6.15 | 24 ± 1.36 |
| BMI, kg/m2 | 24.21 ± 5.54 | 22.33 ± 3.37 |
| Training frequency, hours per week* | 11.71 ± 11.03 | 2.81 ± 1.99 |
Data presented as mean ± SD. BMI, body mass index.
Statistically significant difference between groups (P < .01).
Validity
The face validity of the VISA-P-Ch questionnaire was judged as good by the expert committee. Known-groups validity was demonstrated by significantly lower VISA-P-Ch scores in the patellar tendinopathy group compared with the control group (P < .001) (Table 2). Concurrent validity was demonstrated by the significantly high correlation between VISA-P-Ch scores and Blazina classification in all participants (r = -0.899; P < .001) (Table 2).
Table 2.
Concurrent Validity and Known-Groups Validity a
| Patellar Tendinopathy) | Control | Known-Groups Validity | |
|---|---|---|---|
| First VISA-P-Ch score | 65 ± 11.9 | 98.47 ± 3.04 | -0.899 |
| Blazina classification | 2.03 ± 0.44 | 1 ± 0 | |
| Concurrent Validity (Spearman r)* | -0.899 | ||
Data presented as mean ± SD. VISA-P-Ch, traditional Chinese version of the Victorian Institute of Sport Assessment-Patella.
Statistically significant (P < .001).
Test-Retest Reliability
The results of reliability testing are presented in Tables 3 and 4. The ICC for the VISA-P-Ch was 0.964 overall, with ICCs of 0.86 (95% CI, 0.59-0.95) in the symptomatic group and 0.78 (95% CI, 0.46-0.92) in the control group, indicating good reliability. 12 The SEM was 1.43 for the control group and 4.85 for the patellar tendinopathy group. The minimal detectable change for test-retest reliability was 3.98 for the control group and 13.45 for the patellar tendinopathy group (Table 3). Internal consistency was found to be good for both assessment points (α = 0.834 and 0.851, respectively) (Table 4).
Table 3.
Test-Retest Reliability of VISA-P-Ch a
| Patellar Tendinopathy | Control | |
|---|---|---|
| VISA-P-Ch score | ||
| First assessment | 65 ± 11.9 | 98.47 ± 3.04 |
| Second assessment | 61.7 ± 14.3 | 98.4 ± 3.14 |
| ICC (95% CI) | 0.864 (0.591-0.946) | 0.784 (0.463-0.922) |
| SEM | 4.85 | 1.44 |
| MDC95 | 13.45 | 3.98 |
Data are presented as mean ± SD unless otherwise indicated. CI, confidence interval; ICC, intraclass correlation coefficient; MDC95, minimal detectable change; SEM, standard error of measurement; VISA-P-Ch, traditional Chinese version of the Victorian Institute of Sport Assessment-Patella.
Table 4.
Internal Consistency of the VISA-P-Ch a
| VISA-P-Ch Item | Cronbach α if Item Deleted | |
|---|---|---|
| First VISA-P-Ch Score | Second VISA-P-Ch Score | |
| 1 | 0.829 | 0.831 |
| 2 | 0.812 | 0.827 |
| 3 | 0.812 | 0.827 |
| 4 | 0.787 | 0.818 |
| 5 | 0.815 | 0.815 |
| 6 | 0.783 | 0.820 |
| 7 | 0.821 | 0.850 |
| 8 | 0.876 | 0.907 |
| Cronbach α | 0.834 | 0.851 |
VISA-P-Ch, traditional Chinese version of the Victorian Institute of Sport Assessment-Patella.
Discussion
The major finding of this work indicates that the VISA-P questionnaire was successfully translated and adapted into traditional Chinese, with results showing that the translated version was a reliable and valid tool with which to assess the symptoms of patellar tendinopathy in the Chinese population in this study.
During the pretest period, we consulted 8 participants about the VISA-P-Ch questionnaire, with some misunderstanding and confusion reported for question 4 regarding the words “full weightbearing” and “lunge.” As there is no specific word for “lunge” in Chinese, an illustration of the action to explain what it means was added. We also added a word in Chinese to have a better explanation of “full weightbearing.” The symbol “±” in question 7 also caused confusion as some of the participants could not comprehend its meaning; therefore, “±” was replaced with “and/or” for easier understanding. No other misunderstanding of the questions was reported. The rest of the translation and cross-cultural adaptation, as well as the evaluation of the psychometric properties, was conducted successfully according to guidelines recommended by Beaton et al 2 for the intended Chinese-speaking population.
Known-groups validity was demonstrated by a significant difference in VISA-P-Ch scores between groups where the scores of the symptomatic group were significantly lower than the control group. This result was consistent with the original version and other translated versions of the VISA-P. ††
The concurrent validity of the VISA-P-Ch was demonstrated by a high correlation between the VISA-P-Ch scores and the Blazina classification of participants in this study. This was similar to results reported previously for the German, Greek, and Kannada adaptations of the VISA-P.1,13,16 Although the Blazina classification has been questioned for having only 4 categories for grading the severity level of patellar tendinopathy, it is a disease-specific scale and has been used as a standard for comparing with the VISA-P questionnaire. 4
Test-retest reliability of VISA-P-Ch scores was excellent as a whole (ICC = 0.96), with ICCs of 0.78 in the control group and 0.86 in the symptomatic group. It is acknowledged that the ICC value of the control group was lower than the value of all participants. This might be due to a small within-subject variance in the control group. Nevertheless, the level of measurement reliability for the control group was in the range of good test-retest reliability (ICC > 0.75).
To assess test-retest reliability, a 24- to 48-hour time interval between first and second evaluation was chosen to avoid significant changes in the clinical status of participants. According to a study published by Marx et al, the recommended time interval for test-retest reliability between evaluations was 2 days to 2 weeks. 18 In the French-speaking translation of the VISA-P, a 30-minute time interval was chosen to evaluate test-retest reliability, and showed good reliability (ICC = 0.99). However, the authors also recommended longer time intervals to avoid recall effects. 11 In contrast, a 2.5-week interval was used in the Dutch version of the adaptation and the reliability was still found to be good (ICC = 0.74). Regardless of the varied range of time intervals chosen for the different translated versions of the VISA-P (30 minutes, 2 hours, 24 hours, 1 week, 2 weeks), test-retest reliability has all been reported to be good or excellent (ICC = 0.74-0.99). ‡‡ The consistency of the results showed that the VISA-P questionnaire, including our translated VISA-P-Ch, is a stable and reproducible instrument that can be administered over a period.
The internal consistency of the VISA-P-Ch was 0.83 to 0.85 in this study, which is within the range recommended by Terwee et al 21 (0.7-0.95). The internal consistency of the VISA-P has been validated in other language adaptations of the VISA-P questionnaire, with Cronbach alpha ranging between 0.73 and 0.98, indicating the high degree of homogeneity among items in the questionnaire and no redundant items.1,8,11,13,16,17,23,24
Limitations
There are limitations to our study. The present study was conducted with a limited number of participants in a specific area, which may increase the risk of type 2 error and limit the generalizability of the results. The eligibility of the symptomatic group relied heavily on self-reported signs and symptoms. Given the heterogeneity of patellar tendinopathy, the inclusion of Doppler ultrasound or MRI scans to obtain images of the patellar tendon would have helped to better confirm participant eligibility.
Conclusion
The VISA-P-Ch was proven to be a reliable and valid questionnaire with similar psychometric properties as the original VISA-P questionnaire and can be used in the Chinese-speaking population to assess the severity of symptoms associated with patellar tendinopathy.
Acknowledgments
The authors deeply appreciate all the participants who contributed to this study. The authors also express their sincere gratitude to the Musculoskeletal and Sports Science Laboratory at the National Yang-Ming Chiao-Tung University for its valuable support.
Appendix
Figure A1.
Left, final version of VISA-P-Ch. Right, original VISA-P. VISA-P, Victorian Institute of Sport Assessment-Patella; VISA-P-Ch, traditional Chinese version of the VISA-P.
Final revision submitted August 10, 2023; accepted November 9, 2023.
The authors have declared that there are no conflicts of interest in the authorship and publication of this contribution. AOSSM checks author disclosures against the Open Payments Database (OPD). AOSSM has not conducted an independent investigation on the OPD and disclaims any liability or responsibility relating thereto.
Ethical approval for this study was obtained from the National Yang Ming Chiao Tung University (ref No. YM109067F).
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