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Original Research
DOI: 10.1016/j.bjpt.2018.08.011
Can muscle weakness and disability influence the relationship between pain catastrophizing and pain worsening in patients with knee osteoarthritis? A cross-sectional study
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Ryo Tanakaa,b,
Corresponding author
ryotana@hiroshima-u.ac.jp

Corresponding author. Current address: 1-7-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8521, Japan.
, Kenta Hirohamac, Junya Ozawab
a Graduate School of Integrated Arts and Sciences, Hiroshima University, Hiroshima, Japan
b Department of Rehabilitation, Hiroshima International University, Hiroshima, Japan
c Department of Rehabilitation, Sakamidorii Hospital, Hiroshima, Japan
Highlights

  • We studied the likely mediator between pain catastrophizing and pain worsening.

  • This relationship was mediated by disability and muscle weakness.

  • Cognitive intervention for disability and muscle strengthening may be effective for relieving pain.

This item has received
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Received 01 May 2018, Accepted 13 August 2018
Article information
Abstract
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Figures (2)
Tables (3)
Table 1. The characteristics of participants.
Table 2. Summary measures.
Table 3. Result of correlation analysis.
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Abstract
Objective

To verify if the relationship between pain catastrophizing and pain worsening would be mediated by muscle weakness and disability in patients with symptomatic knee osteoarthritis.

Methods

This was a cross-sectional study in a hospital out-patient setting. Convenience sampling was used with a total of 50 participants with symptomatic knee osteoarthritis. Pain and the activities of daily livings (ADL) were assessed using the Knee Injury and Osteoarthritis Outcome Score (KOOS) subscale. Pain catastrophizing was assessed using the Coping Strategy Questionnaire (CSQ) subscale. Muscle strength of knee extension and 30-s chair stand test (30CST) were also assessed. Path analysis was performed to test the hypothetical model. Goodness of fit of models were assessed by using statistical parameters such as the chi-square value, goodness of fit index (GFI), adjusted goodness of fit index (AGFI), comparative fit index (CFI), and root mean square error of approximation (RMSEA).

Results

The chi-square values were not significant (chi-square=0.283, p=0.594), and the indices of goodness of fit were high, implying a valid model (GFI=1.000; AGFI=0.997; CFI=1.000; RMSEA=0.000). Pain was influenced significantly by muscle strength and ADL; muscle strength was influenced significantly by ADL via 30CST; ADL was influenced by pain catastrophizing.

Conclusion

The relationship between pain catastrophizing with pain worsening are mediated by muscle weakness and disability.

Keywords:
Knee osteoarthritis
Fear-avoidance model
Pain catastrophizing
Muscle weakness
Disability
Full Text
Introduction

Osteoarthritis (OA) is one of the most frequent painful musculoskeletal disorder encountered in the clinic.1 In people with knee OA, pain generally improves with exercise2,3 and/or physical therapy interventions such as hydrotherapy.4 Unfortunately, some people see little to no improvement in pain, whereas others experience chronic pain.5 Cognitive factors seem to be related to chronic pain perception.6 In particular, pain catastrophizing is associated with increasing pain.7 Pain catastrophizing is defined as to the tendency to focus on and magnify pain sensations and to feel helpless in the face of pain.8 However, the reasons for the increasing pain due to pain catastrophizing in people with knee OA have not been fully elucidated.

The fear-avoidance model may help explain chronic pain9–12 and describe how individuals develop chronic musculoskeletal pain as a result of fear-based avoidance behaviors.13,14 Based on this model, pain catastrophizing directly causes pain-related fear.15 People with pain-related fear tend to have a worse performance in activities of daily living,16 which results from avoidance.17 In addition, pain-related fear also leads to muscle weakness,18 which causes disability.19 Lastly, muscular weakness and low physical activity in turn is usually associated with pain worsening.20,21 These findings explain how pain catastrophizing and increased pain would be mediated by muscle weakness and disability in these patients. Pain catastrophizing influences disability and pain in individuals with knee OA.22,23 This has led to the hypothesis that pain worsening in people with knee OA is attributed to pain catastrophizing via muscle weakness and disability.

In patients with early knee OA, decreased muscle strength is associated with an increase in activity limitations.19 Avoidance of activity leads to muscle strength deterioration and consequently to more activity limitations in patients with knee and hip OA.24 However, there is no study showing that the relationship between pain catastrophizing and increased pain would be mediated by muscle weakness and disability. If this model can be shown to apply to patients with symptomatic knee OA, then cognitive intervention focused on muscle weakness and disability may be recommended for these patients. Adding cognitive intervention to exercise can improve functional status more than exercise or cognitive interventions alone.25 Combining exercise and cognitive intervention is expected to suppress pain worsening by improving muscle weakness and reducing disability in individuals with knee OA. The objective of this study was to test the hypothesis that the pain catastrophizing can influence pain intensity via muscular weakness and disability in patients with symptomatic knee OA.

MethodsDesign

This was a cross-sectional study. This study was approved by the ethics committees of the two hospitals where participants were recruited, which were the Sakamidirii Hospital and the Midorii Orthopedic, and the Oasahurusato Hospital, Hiroshima, Japan. The study was carried out in a hospital out-patient setting.

Participants

The inclusion criteria were knee pain and meeting at least three out of six of the following criteria26: age >50 years, morning stiffness <30min, crepitus, bone tenderness, bone enlargement, and no palpable warmth. The exclusion criteria were as follows: (1) presence of articular rheumatism, (2) total arthroplasty, or (3) inability to complete questionnaires independently due to cognitive impairment (e.g. dementia). Convenience sampling was used. The staff of the rehabilitation departments of the two hospitals who were working as physical therapist recruited potential participants and collected data between April 2014 and February 2015. All study participants provided written informed consent. The participants did not receive any compensation for their participation.

Sample size

According to Kline,27 an adequate sample size should always be ten times the number of the parameters in path analysis. As there were five parameters included in the hypothetical models (described below), at least 50 recruited subjects were needed.

MeasuresPain catastrophizing

Pain catastrophizing was assessed using the Coping Strategy Questionnaire (CSQ) subscale developed by Rosenstiel and Keefe.28 The CSQ has been commonly used as an evaluation tool in knee OA research.7 The CSQ is comprised of six subscales evaluating cognitive strategies related to pain (ignoring the pain, reinterpretation of the pain, diverting attention, coping self-statements, catastrophizing, and praying/hoping) and two subscales evaluating behavioral strategies (increasing activity levels and increasing pain behaviors). Of these, subscale for measuring catastrophizing was used in this study. The Japanese version of the CSQ by Ootake and Shimai29 that has its reliability validated was used. The pain catastrophizing subscale consists of two items measured with a numerical rating scale ranging from 0 (never do that) to 6 (always do that) to indicate how frequently these strategies are used to cope with pain.

Muscle strength

Maximal voluntary isometric strength of the bilateral leg during knee extension was measured using a hand-held dynamometer (MT-100, SAKAI Medical Company, Japan). For knee extension, subjects sat in an armless chair and flexed the knee 90°. One end of the strap loop was placed on the shank just above the right lateral malleolus and the other end around the rear leg of the chair. The sole of the foot was about 1cm above the floor. Participants were encouraged to extend their knee joint as much as possible. The same measurement was performed for their bilateral knee joint. The muscle strength recorded was divided by the body weight. Hand-held dynamometry has good to excellent reliability and is valid for most measures of isometric lower limb strength.30

The 30-s chair stand test

The 30-s chair stand test (30CST) was measured to quantify the extent of disability, which result is mainly influenced by impairment of muscle functions in the lower extremity. In the International Classification of Functioning, disability and health (ICF),31 functional ability is included in category of “activity”. Negative condition of the activity referred to an activity limitation that is equivalent to disability in the International Classification of Impairment, Disabilities, and Handicap (ICIDH) model. Accordingly, functional limitation was addressed as a disability (activity limitation) in this study. 30CST was developed originally by Jones et al.32 The participant was seated in the middle of the chair, back straight; feet approximately shoulder width apart and placed on the floor at an angle slightly back from the knees, with one foot slightly in front of the other to help maintain balance. Arms were crossed at the wrists and held against the chest. At the signal “go,” the participant rose to a full stand (body erect and straight) and then returned back to the initial seated position. The participant was encouraged to complete as many full stands as possible within 30s. The participant was instructed to fully sit between each stand. The score was the total number of stands within 30s (more than halfway up at the end of 30s counted as a full stand). Incorrectly executed stands were not counted. Excellent test-retest reliability of 30CST has been confirmed in people with hip and knee OA.33 Criterion validity of 30CST was demonstrated by using the data of the leg press performance32 and the hip and knee isokinetic strength.34

ADL

Another measure used to quantify the extent of disability apart from 30CST was ADL assessment using the ADL subscale of the questionnaire Knee Injury and Osteoarthritis Outcome Score (KOOS).35 The KOOS was developed to assess the patient's opinion on their knee and its associated problems. It holds 42 items in five separately scored subscales: “symptoms”, “pain”, “ADL”, “sport and recreation”, and “quality of life”. A Likert scale was used and items had five possible answer options scored from 0 (no problems) to 4 (extreme problems). According to the KOOS scoring instructions, the KOOS ADL score was transformed to a 0–100 scale, with zero representing extreme knee problems and 100 representing no knee problems. Excellent test-retest reliability of KOOS ADL has been confirmed in people with knee OA.36 The Japanese version of the KOOS by Nakamura et al. that was determined to be both reliable and validity37 was used.

Pain

Pain intensity was assessed using the KOOS pain subscale. Similar to the KOOS ADL score, the Japanese version of the KOOS37 was used. Nine items of the Japanese version for scoring pain were the same as the original version. The KOOS pain score was transformed to a 0–100 scale.

Blinding

In order to reduce the measurement bias, the first author who ideated the study hypothesis did not engage in the recruitment of study subjects and data collection. Hospital staff who collected the data and participants were not informed of the study hypothesis until study completion.

Analysis

Quantitative variables in this study were included in the hypothetical fear-avoidance model as follows: Pain would be influenced by muscle strength, 30CST, and the ADL; muscle strength would be influenced by the ADL via 30CST because muscle weakness are caused by decrease in activity in general; muscle strength, 30CST, and the ADL were influenced by pain catastrophizing. The fitness of the hypothetical model was compared with the alternative model that reverses these causal relations.

The model was tested using the following procedure: first, in order to minimize the variables included in the path analysis, the principal component analysis was performed and the muscle strength data was summarized into one variable. Next, to determine which relationships between variables should be assumed, correlation analysis was performed. Relationships with a p-value ≤0.10 were left in the hypothetical model. Finally, a path analysis was performed to confirm the fitness of both the hypothetical and alternative model. The goodness of fit of the models was assessed by using statistical parameters such as the chi-square value, goodness of fit index (GFI), adjusted goodness of fit index (AGFI), comparative fit index (CFI), root mean square error of approximation (RMSEA), and Akaike's Information Criterion (AIC). A low chi-square value relative to the degrees of freedom with an insignificant p-value (p>0.05), GFI>0.95, AGFI>0.95, CFI>0.95, or RMSEA<0.06 indicated a good model fit.38 AIC was used to compare the hypothetical model with the alternative model where a higher AIC indicated a better overall fitness of the model. If there were subjects with missing data, Little's test was performed to determine whether data was missing completely at random (MCAR), which tests the null hypothesis that the missing data were MCAR.39 A p-value of less than .05 usually indicates that the missing data are not MCAR (i.e., is either missing at random or non-ignorable). In the case of MCAR, Full-Information Maximum Likelihood (FIML) using the expectation-maximization (EM) algorithm was applied to impute estimated data. Statistical analyses were performed using IBM SPSS statistics 22 and IBM SPSS Missing Values (IBM SPSS, Tokyo, Japan) and AMOS 16.0.1.40

Results

A total of 50 subjects participated in our study (Table 1). One participant had missing data for both KOOS pain and KOOS ADL score. Little's test was performed to check whether the missing values occurred at random. We did not reject the null hypothesis that the data were MCAR (p=0.840). Thus, we estimated the value for missing data using the EM algorithm.

Table 1.

The characteristics of participants.

Number50 
Age (year)74.0±10.4 
Gender (female number)37 
Height (average±standard deviation, cm)152.2±7.7 
Body weight (average±standard deviation, kg)54.8±9.0 
The Kellgren–Lawrence grade
23 
12 
Unknowna 
Osteoarthritis  Spine  20 
  Hip 
Complication  Diabetes 
(number)  Hypertension  21 
  Renal failure 
  Cerebral Vascular Disorder 
  Gastrointestinal bleeding 
a

The term “unknown” refers to the people who did not undergo radiographical evaluation.

Summary measures and the results of correlation analysis are shown in Tables 2 and 3, respectively. The p-value of correlation coefficient between muscle strength and pain catastrophizing was larger than 0.10. Furthermore, the p-value of correlation coefficient between pain catastrophizing and pain was smaller than 0.10. From these results, a relationship between muscle strength and pain catastrophizing was excluded from both the hypothetical and alternative model. Moreover, a direct causal relationship between pain catastrophizing and pain was added to these models.

Table 2.

Summary measures.

  Average (standard deviation) 
Pain catastrophizing (0–12)  5.1 (3.0) 
Muscle strength: right (N/kg)  137.9 (72.7) 
Muscle strength: left (N/kg)  135.2 (80.9) 
30CST (times/30s)  11.3 (3.9) 
ADL (0–100)  69.0 (17.7) 
Pain (0–100)  58.9 (19.3) 

ADL, activities of daily livings; 30CST, 30-s chair stand test.

Table 3.

Result of correlation analysis.

  Pain catastrophizing  Muscle strength  30CST  ADL 
Pain catastrophizing         
Muscle strength  −0.142 (0.326)       
30CST  −0.287 (0.044)  0.378 (0.007)     
ADL  −0.440 (0.001)  0.314 (0.026)  0.475 (0.000)   
Pain  −0.242 (0.091)  0.398 (0.004)  0.298 (0.035)  0.815 (0.000) 

Value represents the Pearson's correlation coefficient. Figure between brackets indicates p values.

ADL, activities of daily livings; 30CST, 30-s chair stand test.

The results of path analyses for the hypothetical model are shown in Fig. 1. The chi-square values were not significant (chi-square=0.283, p=0.594), and the indices of goodness of fit were high, implying that the model was validated (GFI=1.000, AGFI=0.997; CFI=1.000, RMSEA=0.000, AIC=28.028). This result did not change significantly even if a subject with missing values was excluded from this path analysis (GFI=1.000, AGFI=0.995, CFI=1.000, RMSEA=0.000, AIC=28.038). Results of this analysis showed that pain was influenced significantly by muscle strength and the ADL; muscle strength was influenced significantly by the ADL via 30CST; and the ADL was influenced by pain catastrophizing. Overall, these results were concordant with the hypothesis that pain intensity was influenced by pain catastrophizing via muscle weakness and disability.

Figure 1.
(0.1MB).

Results of path analysis for the hypothetical model.

The results of path analyses for the alternative model are shown in Fig. 2. There was good fitness of this model (chi-square=0.115, p=0.735, GFI=0.999, AGFI=0.986, CFI=1.000, RMSEA=0.000, AIC=28.115), but the AIC was lower than the hypothetical model.

Figure 2.
(0.1MB).

Results of path analysis for the alternative model.

Discussion

This study focuses on the reasons behind increased pain in people with symptomatic knee OA. We referred to the fear-avoidance model and hypothesized that the relationship between pain catastrophizing and increased pain would be mediated by muscle weakness and disability in patients with symptomatic knee OA. Results of our path analysis supported this hypothesis.

It is known that pain worsening may be caused by loss of the descending pain inhibitory mechanisms in knee OA.41 While lower levels of vigorous and total physical activity inactivates the descending pain inhibitory mechanisms,42 severe pain catastrophizing increased disability22 or muscle weakness via pain-related fear.43 Muscle weakness causes joint instability that promotes an inflammatory intraarticular milieu.44 Our results showing that increased pain was influenced by catastrophizing, weakness, and functional changes may reflect these mechanisms.

Our simplified model showed a significant causal relationship between muscle strength and pain. This result agrees with the high-quality evidence reported in the Cochrane database that muscle strengthening exercises reduced pain.2 Furthermore, our results showed that pain was influenced by the ADL that was emphasized by pain catastrophizing. A randomized placebo-controlled clinical trial reported that cognitive intervention decreased clinical pain in knee OA.45 Our results and the results of this trial suggest that cognitive factors and muscle strength could be an intervention target to reduce pain intensity. Our model could be a rationale for cognitive intervention for pain catastrophizing and muscle strengthening exercises to relieve pain for patients with chronic knee OA.

There are several studies46,47 that have tried to validate the fear-avoidance model. These studies addressed mainly psychological factors such as depressive symptoms, fear-avoidance beliefs, pain-related fear, and pain anxiety. However, they did not focus on factors related to disuse or disability, which is a concept included in the fear-avoidance model. Furthermore, the above studies46,47 collected mainly subjective data using questionnaires that should be carefully examined for psychological bias. In contrast, our study collected objective data of muscle strength using a hand-held dynamometer and 30CST, respectively. We also subsequently validated our results by showing the goodness-of-fit of the model to data, and the significant relationships between each variable supported the hypothesis. Thus, our results are valuable findings that support the validity of the fear-avoidance model, at least in part, in patients with knee OA.

Cognitive intervention can change self-efficacy for managing pain,48 as well as pain catastrophizing. Greater self-efficacy was associated with lower levels of pain and disability.49 These findings support the effectiveness of cognitive intervention in decreasing disability via increasing self-efficacy. In addition, our results from path analysis showed a significant relationship between pain intensity and muscle weakness. It is suggested that pain could also be improved by muscle strengthening without improving ADL level. Several completed randomized controlled trials have supported this effect.2 Thus, cognitive intervention for disability, and muscle strengthening may be valuable tools for pain relief.

There are three limitations in this study. First, this study design was cross-sectional and cannot conclude strict causal relationship. As the fear-avoidance model includes a time course, a longitudinal study design is needed to confirm model validity. Our findings suggesting the validity of this model should be reexamined by a longitudinal study in future. A second limitation is negativity bias, where the convenience sampling used in this study might influence our results. For example, people with negative emotions such as anxiety may produce negative responses. If the ratio of those having such negative emotions in the sample population was larger compared to the target population of knee OA, negative responses might strengthen the correlations among pain catastrophizing, the ADL, and pain that were subjectively scored. The possibility of an overestimate for relationships among these variables should be considered. A third limitation is measurement bias. Muscle weakness was quantified using a hand-held dynamometer, while disability was quantified using 30CST and KOOS ADL. Results using another measurement tool are unknown. In order to reexamine and generalize our finding, future studies should include other measurement tools as indices of muscle weakness and disability.

Conclusion

Pain intensity was influenced by pain catastrophizing via muscle weakness and disability. Cognitive intervention for disability and muscle strengthening may be valuable tools for pain relief.

Funding

This study was funded by the Ministry of Education, Culture, Sports, Science and Technology [Grant-in-Aid for Young Scientists (B)].

Conflicts of interest

The authors declare no conflicts of interest.

References
[1]
L. Sharma,D. Kapoor,S. Issa
Epidemiology of osteoarthritis: an update
Curr Opin Rheumatol, 18 (2006), pp. 147-156 http://dx.doi.org/10.1097/01.bor.0000209426.84775.f8
[2]
M. Fransen,S. McConnell,A.R. Harmer,M. Van der Esch,M. Simic,K.L. Bennell
Exercise for osteoarthritis of the knee
Cochrane Database Syst Rev, 1 (2015), pp. CD004376 http://dx.doi.org/10.1002/14651858.CD004376.pub3
[3]
T. Umehara,R. Tanaka
Effective exercise intervention period for improving body function or activity in patients with knee osteoarthritis undergoing total knee arthroplasty: a systematic review and meta-analysis
Braz J Phys Ther, 22 (2018), pp. 265-275 http://dx.doi.org/10.1016/j.bjpt.2017.10.005
[4]
J.M. Dias,L. Cisneros,R. Dias
Hydrotherapy improves pain and function in older women with knee osteoarthritis: a randomized controlled trial
Braz J Phys Ther, 21 (2017), pp. 449-456 http://dx.doi.org/10.1016/j.bjpt.2017.06.012
[5]
N. Gnanadesigan,R.L. Smith
Knee pain: osteoarthritis or anserine bursitis?
J Am Med Dir Assoc, 4 (2003), pp. 164-166 http://dx.doi.org/10.1097/01.JAM.0000064461.69195.58
[6]
D.M. Urquhart,P.P. Phyomaung,J. Dubowitz
Are cognitive and behavioural factors associated with knee pain? A systematic review
Semin Arthritis Rheum, 44 (2015), pp. 445-455 http://dx.doi.org/10.1016/j.semarthrit.2014.07.005
[7]
R. Tanaka,K. Minamiarita,N. Kito
Are psychological, factors associated with pain worsening in individuals with knee osteoarthritis? A systematic review
J Nov Physiother, 5 (2015), pp. 268
[8]
M.J. Sullivan,B. Thorn,J.A. Haythornthwaite
Theoretical perspectives on the relation between catastrophizing and pain
Clin J Pain, 17 (2001), pp. 52-64
[9]
K. Vangronsveld,M. Peters,M. Goossens,S. Linton,J. Vlaeyen
Applying the fear-avoidance model to the chronic whiplash syndrome
[10]
M.J. Alappattu,M.D. Bishop
Psychological factors in chronic pelvic pain in women: relevance and application of the fear-avoidance model of pain
Phys Ther, 91 (2011), pp. 1542-1550 http://dx.doi.org/10.2522/ptj.20100368
[11]
G. Crombez,C. Eccleston,S. Van Damme,J.W. Vlaeyen,P. Karoly
Fear-avoidance model of chronic pain: the next generation
Clin J Pain, 28 (2012), pp. 475-483 http://dx.doi.org/10.1097/AJP.0b013e3182385392
[12]
G.J. Asmundson,M. Noel,M. Petter,H.A. Parkerson
Pediatric fear-avoidance model of chronic pain: foundation, application and future directions
Pain Res Manag, 17 (2012), pp. 397-405
[13]
J.W. Vlaeyen,S.J. Linton
Fear-avoidance and its consequences in chronic musculoskeletal pain: a state of the art
Pain, 85 (2000), pp. 317-332
[14]
M. Leeuw,M.E. Goossens,S.J. Linton,G. Crombez,K. Boersma,J.W. Vlaeyen
The fear-avoidance model of musculoskeletal pain: current state of scientific evidence
J Behav Med, 30 (2007), pp. 77-94 http://dx.doi.org/10.1007/s10865-006-9085-0
[15]
M. Leeuw,R.M. Houben,R. Severeijns,H.S. Picavet,E.G. Schouten,J.W. Vlaeyen
Pain-related fear in low back pain: a prospective study in the general population
[16]
P.H. Heuts,J.W. Vlaeyen,J. Roelofs
Pain-related fear and daily functioning in patients with osteoarthritis
[17]
A.L. Martin,E. Halket,G.J. Asmundson,D.B. Flora,J. Katz
Posttraumatic stress symptoms and the diathesis-stress model of chronic pain and disability in patients undergoing major surgery
Clin J Pain, 26 (2010), pp. 518-527 http://dx.doi.org/10.1097/AJP.0b013e3181e15b98
[18]
J.S. Thomas,C.R. France,D. Sha,N.V. Wiele
The influence of pain-related fear on peak muscle activity and force generation during maximal isometric trunk exertions
Spine (Phila Pa 1976), 33 (2008), pp. E342-E348
[19]
M. van der Esch,J.F. Holla,M. van der Leeden
Decrease of muscle strength is associated with increase of activity limitations in early knee osteoarthritis: 3-year results from the cohort hip and cohort knee study
Arch Phys Med Rehabil, 95 (2014), pp. 1962-1968 http://dx.doi.org/10.1016/j.apmr.2014.06.007
[20]
K.F. Reid,L.L. Price,W.F. Harvey
Muscle power is an independent determinant of pain and quality of life in knee osteoarthritis
Arthritis Rheumatol, 67 (2015), pp. 3166-3173 http://dx.doi.org/10.1002/art.39336
[21]
R.Z. Pinto,P.H. Ferreira,A. Kongsted,M.L. Ferreira,C.G. Maher,P. Kent
Self-reported moderate-to-vigorous leisure time physical activity predicts less pain and disability over 12 months in chronic and persistent low back pain
[22]
T.J. Somers,F.J. Keefe,J.J. Pells
Pain catastrophizing and pain-related fear in osteoarthritis patients: relationships to pain and disability
J Pain Symptom Manag, 37 (2009), pp. 863-872
[23]
F.J. Keefe,J.C. Lefebvre,J.R. Egert,G. Affleck,M.J. Sullivan,D.S. Caldwell
The relationship of gender to pain, pain behavior, and disability in osteoarthritis patients: the role of catastrophizing
Pain, 87 (2000), pp. 325-334
[24]
M.F. Pisters,C. Veenhof,G.M. van Dijk,J. Dekker,C.S. Group
Avoidance of activity and limitations in activities in patients with osteoarthritis of the hip or knee: a 5 year follow-up study on the mediating role of reduced muscle strength
Osteoarthr Cartil, 22 (2014), pp. 171-177 http://dx.doi.org/10.1016/j.joca.2013.12.007
[25]
K.L. Bennell,Y. Ahamed,G. Jull
Physical therapist-delivered pain coping skills training and exercise for knee osteoarthritis: randomized controlled trial
Arthritis Care Res (Hoboken), 68 (2016), pp. 590-602
[26]
R. Altman,E. Asch,D. Bloch
Development of criteria for the classification and reporting of osteoarthritis. Classification of osteoarthritis of the knee. Diagnostic and Therapeutic Criteria Committee of the American Rheumatism Association
Arthritis Rheum, 29 (1986), pp. 1039-1049
[27]
R. Kline
Principles and Practice of Structural Equation Modeling
Guilford Press, (1998)
[28]
A.K. Rosenstiel,F.J. Keefe
The use of coping strategies in chronic low back pain patients: relationship to patient characteristics and current adjustment
Pain, 17 (1983), pp. 33-44
[29]
K. Ootake,S. Shimai
Pain experiences and coping strategies
Joseigakuhyoron (Women's studies forum), 16 (2002), pp. 143-157
[in Japanese]
[30]
B.F. Mentiplay,L.G. Perraton,K.J. Bower
Assessment of lower limb muscle strength and power using hand-held and fixed dynamometry: a reliability and validity study
[31]
World Health Organization
International Classification of Functioning, Disability and Health: ICF
World Health Organization, (2001)
[32]
C.J. Jones,R.E. Rikli,W.C. Beam
A 30-s chair-stand test as a measure of lower body strength in community-residing older adults
Res Q Exerc Sport, 70 (1999), pp. 113-119 http://dx.doi.org/10.1080/02701367.1999.10608028
[33]
S. Gill,H. McBurney
Reliability of performance-based measures in people awaiting joint replacement surgery of the hip or knee
Physiother Res Int, 13 (2008), pp. 141-152 http://dx.doi.org/10.1002/pri.411
[34]
E.K. McCarthy,M.A. Horvat,P.A. Holtsberg,J.M. Wisenbaker
Repeated chair stands as a measure of lower limb strength in sexagenarian women
J Gerontol A Biol Sci Med Sci, 59 (2004), pp. 1207-1212
[35]
E.M. Roos,S. Toksvig-Larsen
Knee injury and Osteoarthritis Outcome Score (KOOS) – validation and comparison to the WOMAC in total knee replacement
Health Qual Life Outcomes, 1 (2003), pp. 17 http://dx.doi.org/10.1186/1477-7525-1-17
[36]
F. Xie,S.C. Li,E.M. Roos
Cross-cultural adaptation and validation of Singapore English and Chinese versions of the Knee injury and Osteoarthritis Outcome Score (KOOS) in Asians with knee osteoarthritis in Singapore
Osteoarthr Cartil, 14 (2006), pp. 1098-1103 http://dx.doi.org/10.1016/j.joca.2006.05.005
[37]
N. Nakamura,R. Takeuchi,T. Sawaguchi,H. Ishikawa,T. Saito,S. Goldhahn
Cross-cultural adaptation and validation of the Japanese Knee Injury and Osteoarthritis Outcome Score (KOOS)
J Orthop Sci, 16 (2011), pp. 516-523 http://dx.doi.org/10.1007/s00776-011-0112-9
[38]
D. Hooper,J. Coughlan,M. Mullen
Structural equation modelling: guidelines for determining model fit
Electron J Bus Res Methods, 6 (2008), pp. 53-60
[39]
R. Little
A test of missing completely at random for multivariate data with missing values
J Am Stat Assoc, 83 (1988), pp. 1198-1202
[40]
J. Arbuckle
Amos 16.0 User's Guide [Computer software]
Spring House: Amos Development Corporation, (2007)
[41]
E. Lluch Girbes,J. Nijs,R. Torres-Cueco,C. Lopez Cubas
Pain treatment for patients with osteoarthritis and central sensitization
Phys Ther, 93 (2013), pp. 842-851 http://dx.doi.org/10.2522/ptj.20120253
[42]
K.M. Naugle,J.L. Riley 3rd.
Self-reported physical activity predicts pain inhibitory and facilitatory function
Med Sci Sports Exerc, 46 (2014), pp. 622-629 http://dx.doi.org/10.1249/MSS.0b013e3182a69cf1
[43]
S.M. Al-Obaidi,R.M. Nelson,S. Al-Awadhi,N. Al-Shuwaie
The role of anticipation and fear of pain in the persistence of avoidance behavior in patients with chronic low back pain
Spine (Phila Pa 1976), 25 (2000), pp. 1126-1131
[44]
C. Egloff,D.A. Hart,C. Hewitt,P. Vavken,V. Valderrabano,W. Herzog
Joint instability leads to long-term alterations to knee synovium and osteoarthritis in a rabbit model
Osteoarthr Cartil, 24 (2016), pp. 1054-1060 http://dx.doi.org/10.1016/j.joca.2016.01.341
[45]
M.T. Smith,P.H. Finan,L.F. Buenaver
Cognitive-behavioral therapy for insomnia in knee osteoarthritis: a randomized, double-blind, active placebo-controlled clinical trial
Arthritis Rheumatol, 67 (2015), pp. 1221-1233 http://dx.doi.org/10.1002/art.39048
[46]
W.S. Wong,H.M. Lam,P.P. Chen
The fear-avoidance model of chronic pain: assessing the role of neuroticism and negative affect in pain catastrophizing using structural equation modeling
Int J Behav Med, 22 (2015), pp. 118-131 http://dx.doi.org/10.1007/s12529-014-9413-7
[47]
B. Seekatz,K. Meng,J. Bengel,H. Faller
Is there a role of depressive symptoms in the fear-avoidance model? A structural equation approach
Psychol Health Med, 21 (2016), pp. 663-674 http://dx.doi.org/10.1080/13548506.2015.1111392
[48]
J.A. Turner,S. Holtzman,L. Mancl
Mediators, moderators, and predictors of therapeutic change in cognitive-behavioral therapy for chronic pain
[49]
H. Brister,J.A. Turner,L.A. Aaron,L. Mancl
Self-efficacy is associated with pain, functioning, and coping in patients with chronic temporomandibular disorder pain
J Orofac Pain, 20 (2006), pp. 115-124
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Brazilian Journal of Physical Therapy

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