This item is the archived peer-reviewed author-version of:

Clinimetric properties of illness perception questionnaire revised (IPQ-R) and brief

illness perception questionnaire (Brief IPQ) in patients with musculoskeletal
disorders : a systematic review

Reference:
Leysen Marijke, Nijs Jo, Meeus Mira, Van Wilgen C. Paul, Struyf Filip, Vermandel Alexandra, Kuppens An,
Roussel Nathalie.- Clinimetric properties of illness perception questionnaire revised (IPQ-R) and brief illness
perception questionnaire (Brief IPQ) in patients with musculoskeletal disorders : a systematic review
Manual therapy / Manipulation Association of Chartered Physiotherapists - ISSN 1356-689X - (2014), p. 1-35
DOI: http://dx.doi.org/doi:10.1016/j.math.2014.05.001

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Accepted Manuscript

Clinimetric properties of illness perception questionnaire revised (IPQ-R) and brief

illness perception questionnaire (Brief IPQ) in patients with musculoskeletal disorders:
A systematic review

Marijke Leysen , Jo Nijs , Mira Meeus , C. Paul van Wilgen , Filip Struyf , Alexandra
Vermandel , Kevin Kuppens , Nathalie Roussel
PII: S1356-689X(14)00084-8
DOI: 10.1016/j.math.2014.05.001
Reference: YMATH 1566

To appear in: Manual Therapy

Received Date: 19 December 2013

Revised Date: 4 April 2014
Accepted Date: 6 May 2014

Please cite this article as: Leysen M, Nijs J, Meeus M, Paul van Wilgen C, Struyf F, Vermandel A,
Kuppens K, Roussel N, Clinimetric properties of illness perception questionnaire revised (IPQ-R) and
brief illness perception questionnaire (Brief IPQ) in patients with musculoskeletal disorders: A systematic
review, Manual Therapy (2014), doi: 10.1016/j.math.2014.05.001.

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 ACCEPTED MANUSCRIPT
Clinimetric properties of illness perception questionnaire

revised (IPQ-R) and brief illness perception questionnaire

(Brief IPQ) in patients with musculoskeletal disorders: A

systematic review

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Marijke Leysen ab, Jo Nijs bce, Mira Meeus abg, C. Paul van Wilgen bd, Filip Struyf abc,

Alexandra Vermandel af, Kevin Kuppens abc, Nathalie Roussel abc

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a
Rehabilitation Sciences and Physiotherapy (REVAKI), Faculty of Medicine and Health Sciences, University of

Antwerp, Antwerp, Belgium

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b
Pain in Motion Research Group (www.paininmotion.be)
c
Departments of Human Physiology and Physiotherapy, Faculty of Physical Education and Physiotherapy, Vrije
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Universiteit Brussel, Belgium

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Transcare, Transdisciplinary Pain Management Centre, the Netherlands.
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Department of Physical Medicine and Physiotherapy, University Hospital Brussels, Belgium
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Department of Urology, University Hospital Antwerp, Belgium
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Ghent University Hospital (6K3) (REVAKI), Faculty of Medicine, Ghent University
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Corresponding author: Nathalie Roussel;

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Address of correspondence and reprints requests to Nathalie Roussel, Universiteit Antwerpen, Campus Drie
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Eiken D.S.121, Universiteitsplein 1, 2610 Wilrijk, Belgium (e-mail: [email protected]; phone:

+3232652859; website: www.paininmotion.be

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1 ABSTRACT

2 Several questionnaires are available to evaluate illness perceptions in patients, such as the

3 illness perception questionnaire revised (IPQ-R) and the brief version (Brief IPQ). This

4 study aims to systematically review the literature concerning the clinimetric properties of

5 the IPQ-R and the Brief IPQ in patients with musculoskeletal pain. The electronic

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6 databases Web of Sciences and Pubmed were searched. Studies were included when the

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7 clinimetric properties of the IPQ-R or Brief IPQ were assessed in adults with

8 musculoskeletal pain. Methodological quality was determined using the COSMIN

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9 checklist. Eight articles were included and evaluated. The methodological quality was

10 good for 3 COSMIN boxes, fair for 11 and poor for 3 boxes. None of the articles obtained

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an excellent methodological score. The results of this review suggest that the IPQ-R is a
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12 reliable questionnaire, except for illness coherence. Internal consistency is good, except for
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13 the causal domain. The IPQ-R has good construct validity, but the factor structure is

14 unstable. Hence, the IPQ-R appears to be a useful instrument for assessing illness
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15 perceptions, but care must be taken when generalizing the results of adapted versions of
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16 the questionnaires. The Brief IPQ shows moderate overall test-retest reliability. No articles

17 examining the validity of the Brief IPQ were found. Further research should therefore
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18 focus on the content and criterion validity of the IPQ-R and the clinimetric properties of

19 the Brief IPQ.

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20

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24 Key Words: musculoskeletal pain (MeSH), epidemiologic methods (MeSH),

25 Questionnaires (MeSH), Perception (MeSH)

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1 INTRODUCTION

2 Recent guidelines advise health care personal to evaluate and treat patients with

3 musculoskeletal pain from a biopsychosocial perspective (Airaksinen et al., 2006; Tulder

4 et al., 2006). In both medical and psychological literature, Leventhal’s Common Sense

5 Model (CSM) is often used as a theoretical framework for the evaluation and treatment of

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6 patients (Leventhal et al., 2003). According to this model, patients develop cognitions

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7 about their illness, based on former experiences, interpretation of symptoms and provided

8 information. These cognitions are often referred to as illness perceptions.

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10 These illness perceptions have been studied in several pathologies such as cardiovascular

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disorders (Schoormans et al., 2013), respiratory disorders (Kaptein et al., 2011) and
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12 musculoskeletal disorders e.g. fibromyalgia (van Wilgen et al., 2008), sports injuries (van
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13 Wilgen et al., 2010; Larmer et al., 2011), low back pain (Foster et al., 2008; van Wilgen et

14 al., 2012), chronic fatigue syndrome and rheumatoid arthritis (Moss-Morris & Chalder,
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15 2003). Especially when there is no clear diagnosis (e.g. no bodily cause of pain or
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16 medically unexplained symptoms), patients form their own interpretation of symptoms to

17 explain the disorder. Illness perceptions will determine the patient’s coping strategy.
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18 (Sumathipala et al., 2008). Some patients will typically develop negative beliefs about their

19 illness (Stenner et al., 2000). These negative illness perceptions can include believing that
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20 the problem will last long, relating all symptoms to their illness or having weak beliefs

21 about self-control and low confidence in performing activities despite their pain (Foster et

22 al., 2008). In a large prospective study with acute, sub-acute and chronic low back pain

23 patients, negative illness perceptions were better predictors of disability at 6 months than

24 fear avoidance, catastrophizing or depression (Foster et al., 2008; Foster et al., 2010). In

25 chronic pain patients, negative illness perceptions are associated with maladaptive illness
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26 behaviour, dysfunction, poor treatment adherence and treatment outcome (Spinhoven et al.,

27 2004; Edwards et al., 2006).

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29 In order to evaluate illness perceptions, the Illness Perceptions Questionnaire (IPQ)

30 (Weinman et al., 1996) was developed. Subsequent to publication of the IPQ, further

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31 evolvement of the tool was undertaken, leading to the creation of the IPQ-Revised (IPQ-R)

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32 (Moss-Morris et al., 2002). The IPQ-R measures 9 dimensions of illness perceptions and

33 consists of 3 domains. In the first domain, called illness identity, the perceived symptoms

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34 and their possible relation to the illness are evaluated. The second domain, the beliefs

35 domain, covers 7 dimensions: the acute/chronic timeline as well as the cyclical character of

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the illness represent the first and second dimension. Consequences, as the third dimension,
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37 include perceived short- and long-term effects on physical, psychological and social
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38 functioning. Controllability and curability refers to the extent to which a condition is

39 perceived to be controllable or curable, while emotional representations, the sixth

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40 dimension, represent the emotions experienced as a result of their illness. Finally, illness
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41 coherence reflects an individual’s understanding of their condition. For each dimension,

42 responders rate their level of agreement on a five-point Likert scale, ranging from ‘strongly
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43 disagree’ to ‘strongly agree’. The third domain lists 18 possible causes to which

44 individuals attribute their condition, the degree to which individuals perceive themselves as
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45 responsible for the illness, as well as the responsibility individuals take for curing

46 themselves. Again, patients rate their level of agreement on a five-point Likert scale,

47 ranging from ‘strongly disagree’ to ‘strongly agree’ (Hill et al., 2007).

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49 In 2006 Broadbent et al. constructed a briefer version from the IPQ-R, which is referred to

50 as the Brief IPQ (Broadbent et al., 2006). The aim was to construct a very short and simple
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51 measure of illness perceptions for clinical use and to provide an alternative for the 5-point

52 Likert scale approach. The Brief IPQ is an eight-item instrument that measures the

53 cognitive perceptions with respect to an illness on an ordinal scale (0–10). Eight areas are

54 examined: consequences (item 1), timeline (item 2), personal control (item 3), treatment

55 control (item 4), identity for describing the condition and symptoms (item 5), coherence

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56 (item 7), and concern and emotions (items 6 and 8). The maximal score on the Brief IPQ is

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57 80, where higher scores reflect more negative perceptions.

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59 Since the IPQ, IPQ-R and Brief IPQ are general questionnaires, researchers are allowed to

60 substitute the term ‘illness’ with the name of the condition they are investigating

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(Weinman et al., 1996; Hill et al., 2007). Moreover, researchers should feel free to modify
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62 the causal and identity scales in order to suit particular illnesses, cultural settings or
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63 populations (Moss-Morris et al., 2002).

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65 Because illness perceptions are measured in a variety of disorders, the questionnaires can
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66 be adapted in function of each condition, such as fibromyalgia (Van Wilgen et al., 2008)

67 and hand injury (Chan et al., 2009). However, information regarding the clinimetric
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68 properties of the (adapted versions of the) IPQ-R and Brief IPQ is lacking. The clinimetric

69 approach is directed at the development of instruments to measure multiple constructs with

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70 a single index (Fayers & Hand, 2002), which is often the case in clinical practice (Vet et

71 al., 2003). It is associated with rating scales that are used to describe or measure

72 symptoms, physical signs and other distinctly clinical phenomena (Feinstein, 1983; 1987).

73 A summary of the quality of the studies that have investigated IPQ-R or Brief IPQ will

74 give perspective on how these articles can assist in directing approaches in clinical

75 practice. Therefore, the aim of the present literature overview was to systematically review
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76 the clinimetric properties of the IPQ-R and the Brief IPQ in patients with musculoskeletal

77 disorders.

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79 METHODS

80 Search strategy

81 Full details of the search strategy can be found in the addendum. In brief, alongside

82 adherence to the PRISMA guidelines, the PICOS model was used to list three groups of

83 keywords: (P) patients with musculoskeletal pain, (I) IPQ-R or Brief IPQ and (O)

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84 clinimetric properties. No limits were added.

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86 Methodological quality of the included articles

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87 The methodological quality of the included articles was reviewed using the COSMIN

88 checklist with 4-point rating scale, representing excellent, good, fair and poor

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methodological quality (Mokkink et al., 2010a). The COSMIN checklist is a standardized
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90 tool for assessing the methodological quality of studies on measurement properties. It
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91 contains a generalizability box and 9 separate boxes, each dealing with one measurement

92 property, with 5-18 items per box about the design and statistical methods. This
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93 incorporates potential bias of individual studies. Two researchers independently scored the
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94 selected studies. After reviewing the articles, the results of both researchers were compared

95 and differences were discussed until consensus was obtained. Subsequently, a

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96 methodological quality score per box is obtained by taking the lowest rating of any item in

97 a box (Terwee et al., 2012). The results were evaluated using the quality criteria for
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98 measurement properties of health status questionnaires described by Terwee et al. (Terwee

99 et al., 2007).

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101 Outcome measurements

102 For the purpose of this study reliability was analysed in terms of internal consistency and

103 test-retest reliability (Lohr et al., 1996). Internal consistency is a measure of the extent to
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104 which items in a subscale are correlated, thus measuring the same concept (Terwee et al.,

105 2007). To express the internal consistency of the different items in the domains of the IPQ-

106 R, Cronbach’s alphas can be calculated. A Cronbach’s alpha above 0.80 is considered to be

107 acceptable (Dijkers et al., 2002). Reproducibility or test–retest reliability over a period of

108 time can be calculated using an intraclass correlation coefficient (ICC), a weighted kappa

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109 or Pearson correlation. To interpret the kappa statistics, values above 0.60 are considered

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110 substantial agreement (Landis & Koch, 1977). For ICC, the threshold value of 0.75 for

111 good reliability was used (Portney & Watkins, 2000). For Pearson's correlations, critical

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112 values are subject to the number of correlated items (Fisher & Yates, 1974; Portney &

113 Watkins, 2000).

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115 Validity will be presented as construct-, content- and criterion-related validity (Lohr et al.,
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116 1996; Mokkink et al., 2010b). Construct validity refers to the ability of an instrument to

117 measure a concept or construct. Convergence, discrimination, factor analysis, hypothesis

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118 testing and known groups method are procedures to gather information about the construct
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119 (Portney & Watkins, 2000). According to the COSMIN taxonomy, construct validity is

120 divided into hypotheses testing, structural validity and cross-cultural validity (Mokkink et
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121 al., 2010b). Content validity is the degree to which the content of an instrument is an

122 adequate reflection of the construct to be measured (Mokkink et al., 2010b). Concurrent
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123 validity is an aspect of criterion validity and measures the agreement between the results

124 obtained by the IPQ-R and the results obtained by another instrument within the same

125 population at the same time.

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126 RESULTS

127 Search strategy

128 The initial search strategy identified 75 unique abstracts from the PubMed and Web of

129 Science databases. Two articles were included by hand search. Based on the inclusion criteria,

130 65 abstracts were excluded. Figure 1 presents a flowchart of the search strategy. A detailed

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131 overview of the included articles is presented in Table 1. The full text version of all papers

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132 that met the inclusion criteria was retrieved for quality assessment and data extraction.

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134 Eight studies were included (Table 1) and scored for their methodological quality (Table 2).

135 The methodological quality of the different items of the studies varied from good (van

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Ittersum et al., 2009; Nicholls et al., 2013) to fair (Moss-Morris et al., 2002; van Wilgen et al.,
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137 2008; Chan et al., 2009; Glattacker et al., 2009; Albert et al., 2013; Hallegraeff et al., 2013) to
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138 poor (Chan et al., 2009; Hallegraeff et al., 2013).

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140 Seven studies analysed the clinimetric properties of the IPQ-R (Moss-Morris et al., 2002; van
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141 Wilgen et al., 2008; Chan et al., 2009; Glattacker et al., 2009; van Ittersum et al., 2009; Albert

142 et al., 2013; Nicholls et al., 2013). Only one study administered the Brief IPQ (Hallegraeff et
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143 al., 2013). To target a specific patient population, the IPQ-R was adapted in each article.

144 These changes are presented in table 3.

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146 Methodological quality of the included articles

147 The assessment of methodological quality of the included articles is shown in Table 2.

148 Agreement between the two researchers was 83%. Consensus was obtained on all items. The

149 answers on the generalizability box of the COSMIN checklist of each article are presented in

150 Table 1. The items with poor methodological quality will not be further discussed.
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151

152 Reliability

153 The Pearson correlations for test-retest reliability varied between 0.50 and 0.87 for the beliefs

154 domain, except for cyclical timeline, where a lower correlation was observed (0.35). For

155 illness identity and the causal domain, the correlations varied between 0.24-0.57 and 0.53-

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156 0.85, respectively (Table 4). The ICC varied between 0.55 and 0.87 (Glattacker et al., 2009).

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157 The test-retest reliability of the Brief IPQ over a one-week period was acceptable (ICC 0.72,

158 95% CI:0.53-0.82) (Hallegraeff et al., 2013).

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160 Internal consistency of the beliefs domain of the IPQ-R among different patient populations

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was satisfactory, ranging between 0.51 and 0.87 (table 4). Of the sub-domains within the
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162 causal domain, only psychological attributions presented an alpha ≥0.82. The sub-domain
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163 ‘accident or chance’ showed a very low internal consistency. No studies examined the internal

164 consistency of the Brief IPQ.

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166 The measurement error was evaluated in the Brief IPQ only (Hallegraeff et al., 2013). Limits

167 of agreement ranged from -25.3 to 17.1. No systematic trend was visible in the Bland-Altman
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168 plot. The standard error of the mean was 1.17 and the smallest detectable change was 42,

169 compared to a maximum score of 80 (Hallegraeff et al., 2013).

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170

171 Validity

172 Three articles tested different hypotheses on the construct validity of the IPQ-R (van Wilgen

173 et al., 2008; Chan et al., 2009; Albert et al., 2013) (table 5).

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175 Three studies established structural validity of the IPQ-R as an aspect of construct validity

176 (Moss-Morris et al., 2002; van Ittersum et al., 2009; Nicholls et al., 2013). Moss-Morris et al.

177 used an independent samples t-test to explore known group validity within acute versus

178 chronic patients (Moss-Morris et al., 2002). Chronic pain patients were significantly different

179 from acute patients on all dimensions of the IPQ-R (p<.001), except for risk factor attributions

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180 (p<.01).

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181 Two studies performed a factor analysis: one study used both an exploratory and confirmatory

182 factor analysis (Nicholls et al., 2013) while the other used confirmatory factor analysis only

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183 (van Ittersum et al., 2009). Results are presented in table 6.

184 No studies assessed the validity of the Brief IPQ.

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186 DISCUSSION

187 The results of this review suggest that the IPQ-R is a reliable questionnaire, except for the

188 illness coherence, with good internal consistency, except for the causal domain. The IPQ-R

189 demonstrates good construct validity, but the factor structure is unstable. The Brief IPQ shows

190 moderate overall test-retest reliability. There is a lack of articles studying the validity of the

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191 Brief IPQ used in musculoskeletal conditions.

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193 Methodological quality of the included articles

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194 The methodological quality of the different items of the included studies ranged from poor

195 (N=3) to good (N=3). Methodological problems included an insufficient sample size,

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selection bias (e.g. convenience sampling), lack of description of handling with missing data
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197 or the lack of a priori formulated hypotheses. The items with poor methodological quality
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198 were eliminated from this literature review, since the precision of the results in these articles

199 is doubtful. None of the selected articles obtained an excellent methodological score,
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200 implying that all included studies had methodological flaws.

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202 Test-retest reliability

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203 The results of the present study suggest that test-retest reliability of the IPQ-R and Brief IPQ

204 is acceptable in the observed patient populations. Two out of three articles only calculated
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205 Pearson correlations (Moss-Morris et al., 2002; van Wilgen et al., 2008). Pearson correlation

206 coefficients are less accurate to measure reliability than ICC, because systematic differences

207 are not taken into account (Streiner & Norman, 2003). The moderate ICC in one study

208 evaluating orthopaedic patients (Glattacker et al., 2009) suggests that further research is

209 necessary to improve the test-retest reliability.

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210 To measure test-retest reliability, it is important to ensure the stability of the illness

211 perceptions of the patients within the time frame. Therefore, it must be questioned whether

212 illness perceptions remain stable over time if symptoms are fluctuating. The differences in

213 test-retest reliability across studies might be explained by the time interval between the

214 consecutive measurements, which was much longer (6 months) in the study by Moss-Morris

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215 et al. (2002) compared to the 3 weeks (van Wilgen et al., 2008) or 4 days-time interval

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216 (Glattacker et al., 2009) in other studies.

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218 The single study examining test-retest reliability of the Brief IPQ (Hallegraeff et al., 2013)

219 suggests an acceptable test-retest reliability. In that study, the smallest detectable change was

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42, which means that a change in the Brief IPQ overall score must exceed a value of 42 in
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221 order to reflect a true difference between test and retest scores. With a maximum overall score
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222 of 80, it can be suggested that the Brief IPQ is not suitable for detecting real individual

223 changes. However, it can also be questioned if an overall score can be calculated in the Brief
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224 IPQ, for each question measures a different dimension of illness perceptions.
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226 Internal consistency

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227 The Cronbach's alphas for the beliefs domain of the IPQ-R showed good internal consistency

228 (0.75-0.82). Two studies had lower scores on some of the subscales (van Wilgen et al., 2008;
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229 Albert et al., 2013). This may be related to the smaller sample size in comparison to the third

230 study (van Ittersum et al., 2009). The latter had a good methodological quality. Furthermore,

231 Albert et al. created a virtually new questionnaire by adding 26 items to the beliefs domain,

232 making it hazardous to compare.

233 Illness identity consists of disparate symptoms, such as pain, fatigue, nausea and stiff joints.

234 Some symptoms may be more relevant to particular illnesses than other symptoms (e.g. stiff
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235 joints is common for fibromyalgia, but less common for low back pain (van Wilgen et al.,

236 2008; van Ittersum et al., 2009; van Wilgen et al., 2012)). Therefore, the internal consistency

237 of this scale is less relevant than in the other subscales. Symptoms and their frequency are

238 presented as a checklist, therefore they are not supposed to measure a certain construct.

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240 Within the causal domain, internal consistency is very good for the psychological attribution

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241 (0.82-0.90). The Cronbach's alphas for the other subscales in the causal domain are moderate

242 (0.47-0.62), except for accident or chance, which are very low (0.00-0.14). By analogy with

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243 symptoms, causes can be very diverse between different pathologies. Again, some causes may

244 be more relevant to particular illnesses than other (e.g. 'hereditary' is often cited as a cause in

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fibromyalgia, whereas it is not mentioned frequently by patients with low back pain (van
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246 Ittersum et al., 2009; van Wilgen et al., 2012)). This is supported by the unstable factor
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247 structure of the causal domain (Nicholls et al., 2013). It is suggested that a satisfactory factor

248 solution could be found if the list of causal items is sufficiently modified to relate more
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249 clearly to musculoskeletal pain patients, by removing items or including new items (Nicholls
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250 et al., 2013).

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252 Construct validity

253 The significant differences in test results between acute and chronic patients on all dimensions
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254 reflect clear known group validity (Moss-Morris et al., 2002). In patients with fibromyalgia,

255 catastrophizing showed a negative relationship with illness coherence and a positive

256 association with emotional representations and cyclical timeline (van Wilgen et al., 2008),

257 suggesting that patients who do not have a clear understanding of their situation have the

258 tendency to catastrophize. This indicates that education and information play a key role in the

259 treatment process.

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260

261 However, pain intensity proves to be unrelated to the subscales of the IPQ-R in patients with

262 musculoskeletal disorders which are absent from work (Albert et al., 2013). In this particular

263 patient population, pain intensity might be of less importance compared to functional

264 limitations. This is reflected in the fact that a high illness identity endorsed by participants is

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265 more strongly associated with psychological distress than with pain intensity (Albert et al.,

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266 2013).

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268 Structural validity of the IPQ-R was assessed in two articles with good methodological quality

269 (van Ittersum et al., 2009; Nicholls et al., 2013). The factor structure of the beliefs domain as

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suggested in the original IPQ-R (Moss-Morris et al., 2002) could not be completely affirmed,
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271 nor could the causal domain. The factor structure of the original IPQ-R was calculated in 711
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272 patients with a variety of disorders, such as rheumatoid arthritis, type II diabetes, asthma,

273 chronic pain, acute pain, multiple sclerosis, myocardial infarction and HIV (Moss-Morris et
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274 al., 2002). Comparison of the clinimetric properties of the questionnaires should ideally be
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275 calculated in a homogeneous patient group. For the causal domain, this may be even more

276 important, as attributions are probably disease specific. Another potential reason why the
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277 seven-factor model of the beliefs domain does not generally provide a good fit could be

278 related to the presentation of the items. A mixture of positively and negatively worded items
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279 may confuse some respondents. There is some evidence that positively worded items are more

280 highly correlated with each other than negatively worded items, and vice-versa (Nicholls et

281 al., 2013).

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283 There is a lack of studies with good methodological quality examining the measurement error

284 and predictive validity of the IPQ-R. This would favour the use of this type of questionnaires
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285 in clinical practice. Furthermore, no studies with good methodological quality examined the

286 criterion validity or content validity of the IPQ-R. Concerning the Brief IPQ, only one article

287 met the inclusion criteria (Hallegraeff et al., 2013). This suggests the need of future research

288 to study the clinimetric properties of the Brief IPQ within musculoskeletal patients more

289 closely.

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291 Study limitations

292 Since the aim of present study was to identify clinimetric properties of the IPQ-R or Brief IPQ

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293 within musculoskeletal patients, the results of this review are only applicable to the included

294 populations. Furthermore, it is uncertain whether clinimetric qualities of translated versions

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can be generalized to the original version. The results of the present study are therefore only
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296 applicable to the questionnaire and language used in a particular study (table 1). It has to be
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297 noted that none of the included articles had an excellent score on the COSMIN checklist for

298 methodological quality. Therefore the results of the articles should not be rejected, but one
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299 must be attentive to the interpretation. As the first and third domain (i.e. illness identity and
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300 causal domain) are adjustable by researchers, care must be taken when comparing or

301 generalizing the results of adapted questionnaires. In the last question of the IPQ-R, patients
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302 are asked to describe the three most important causes for their illness. With this open-ended

303 format, a wealth of information is obtained from the patients, but due to the design it is very
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304 difficult to objectify, measure or compare these results. Nevertheless, the latter is very

305 interesting for clinical practice, given the fact that negative illness perceptions influence

306 behaviour (Leventhal et al., 2003) and predict disability in low back pain patients (Foster et

307 al., 2008; Foster et al., 2010).

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309 Conclusion
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310 The results of the present systematic review confirm that the IPQ-R is an appropriate

311 instrument to explore illness beliefs in patients with musculoskeletal disorders. Since the

312 questionnaire can be adapted to target a specific patient population, the factor structure

313 remains a delicate issue. Further research should be conducted to optimise the clinimetric

314 properties of the Brief IPQ in patients with musculoskeletal disorders.

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317 REFERENCES

318 Airaksinen, O, Brox, J, Cedraschi, C, Hildebrandt, J, Klaber-Moffett, J, Kovacs, F, Mannion,

319 A, Reis, S, Staal, J, Ursin, H, Zanoli, G. Chapter 4: European guidelines for the
320 management of chronic nonspecific low back pain Eur Spine J. 2006; (15): Suppl
321 2:S192-300.
322 Albert, V, Coutu, MF, Durand, MJ. Internal consistency and construct validity of the Revised
323 Illness Perception Questionnaire adapted for work disability following a
324 musculoskeletal disorder. Disabil Rehabil 2013; 35(7): 557-65.

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325 Broadbent, E, Petrie, KJ, Main, J, Weinman, J. The brief illness perception questionnaire. J
326 Psychosom Res 2006; 60(6): 631-7.
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335 325-32.
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341 Feinstein, AR. Clinimetrics New Haven, Connecticut: Yale University Press, 1987;
342 Fisher, RA, Yates, F. Statistical tables for biological, agricultural and medical research, 6th
343 revised and enlarged ed. UK: Longman, 1974;
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344 Foster, NE, Bishop, A, Thomas, E, Main, C, Horne, R, Weinman, J, Hay, E. Illness
345 perceptions of low back pain patients in primary care: what are they, do they change
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347 Foster, NE, Thomas, E, Bishop, A, Dunn, KM, Main, CJ. Distinctiveness of psychological
348 obstacles to recovery in low back pain patients in primary care. Pain 2010; 148(3):
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349 398-406.
350 Glattacker, M, Bengel, J, W.H., J. German version of the Illness perception questionnaire-
351 revised. Zeitschrift für Gesundheitspsychologie 2009; 17(4): 158-169.
352 Hallegraeff, JM, van der Schans, CP, Krijnen, WP, de Greef, MH. Measurement of acute
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353 nonspecific low back pain perception in primary care physical therapy: reliability and
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356 Hill, S, Dziedzic, K, Thomas, E, Baker, SR, Croft, P. The illness perceptions associated with
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359 (Oxford) 2007; 46(6): 944-51.
360 Kaptein, AA, Yamaoka, K, Snoei, L, Kobayashi, K, Uchida, Y, van der Kloot, WA, Tabei, T,
361 Kleijn, WC, Koster, M, Wijnands, G, Kaajan, H, Tran, T, Inoue, K, van Klink, R, van
362 Dooren-Coppens, E, Dik, H, Hayashi, F, Willems, L, Annema-Schmidt, D, Annema,
363 J, van der Maat, B, van Kralingen, K, Meirink, C, Ogoshi, K, Aaronson, N, Nortier, H,
364 Rabe, K. Illness perceptions and quality of life in Japanese and Dutch patients with
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367 Biometrics 1977; 33(1): 159-74.
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371 Leventhal, H, Brissette, I, Leventhal, E. The common-sense model of self-regulation of health
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373 illness behavior New York: Routledge, 2003.
374 Lohr, KN, Aaronson, NK, Alonso, J, Burnam, MA, Patrick, DL, Perrin, EB, Roberts, JS.

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378 Vet, HC. The COSMIN checklist for assessing the methodological quality of studies
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381 Mokkink, LB, Terwee, CB, Patrick, DL, Alonso, J, Stratford, PW, Knol, DL, Bouter, LM, de
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385 Moss-Morris, R, Chalder, T. Illness perceptions and levels of disability in patients with
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388 Moss-Morris, R, Weinman, J, Petrie, KJ, Horne, R, Cameron, LD, Buick, D. The revised
389 illness perception questionnaire (IPQ-R). Psychology and Health 2002; 17(1): 1-16.
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390 Nicholls, EE, Hill, S, Foster, NE. Musculoskeletal pain illness perceptions: factor structure of
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394 Schoormans, D, Mulder, BJ, van Melle, JP, Pieper, PG, van Dijk, AP, Sieswerda, GT,
395 Hulsbergen-Zwarts, MS, Plokker, TH, Brunninkhuis, LG, Vliegen, HW, Sprangers,
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396 MA. Illness perceptions of adults with congenital heart disease and their predictive
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398 Spinhoven, P, Ter Kuile, M, Kole-Snijders, AM, Hutten Mansfeld, M, Den Ouden, DJ,
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399 Vlaeyen, JW. Catastrophizing and internal pain control as mediators of outcome in the
400 multidisciplinary treatment of chronic low back pain. Eur J Pain 2004; 8(3): 211-9.
401 Stenner, PH, Dancey, CP, Watts, S. The understanding of their illness amongst people with
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410 Terwee, CB, Bot, SD, de Boer, MR, van der Windt, DA, Knol, DL, Dekker, J, Bouter, LM, de
411 Vet, HC. Quality criteria were proposed for measurement properties of health status
412 questionnaires. J Clin Epidemiol 2007; 60(1): 34-42.
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414 methodological quality in systematic reviews of studies on measurement properties: a
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417 E, Malmivaara, A. Chapter 3: European guidelines for the management of acute
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425 chronic low back pain differ from people without chronic low back pain?
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428 patients with fibromyalgia and their relationship to quality of life and catastrophizing.
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431 coin. Journal of Clinical Epidemiology 2003; 56: 1146–1147.
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434

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1 ADDENDUM: SEARCH STRATEGY

3 Using the PRISMA guidelines (Liberati et al., 2009), a systematic search strategy was

4 performed via the electronic databases PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) and

5 Web of Science (http://isiwebofknowledge.com) from their inception up till April 2013.

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6 Several key word combinations were made to ensure that no relevant articles were missed.

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7 Using the PICOS (Population, Intervention, Comparison, Outcome, Study design) model,

8 three groups of keywords were listed: (P) patients with musculoskeletal pain, (I) IPQ-R or

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9 Brief IPQ and (O) clinimetric properties. The keywords from the three groups were combined.

10 No limits were used during the search strategy.

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12 To identify relevant articles, all titles and/or abstracts of the selected articles were screened
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13 for inclusion. Articles were eligible for this review if they fulfilled the following criteria: 1)

14 the study consisted of a prospective, population-based cohort or case-control design

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15 investigating the clinimetric properties of the IPQ-R or Brief IPQ, 2) subjects of the study
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16 were adult patients (18 years and older) with musculoskeletal complaints, and 3) the studies

17 were written in English, German, French or Dutch. Articles were excluded from this
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18 systematic literature research if they were letters to the editor or reviews, abstracts,

19 hypotheses or papers without scientific data or if they included only healthy subjects. In case
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20 of doubt of the eligibility of the article based on the content of the title and abstract, the full

21 text version was retrieved and evaluated against the selection criteria as mentioned above.

22 Literature was screened by the first and last author.

23

24 Liberati, A, Altman, DG, Tetzlaff, J, Mulrow, C, Gotzsche, PC, Ioannidis, JP, Clarke, M,
25 Devereaux, PJ, Kleijnen, J, Moher, D. The PRISMA statement for reporting
26 systematic reviews and meta-analyses of studies that evaluate health care
27 interventions: explanation and elaboration. PLoS Med 2009; 6(7): e1000100.
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There are no conflicts of interest to report. The study was funded by the research council of

Artesis University College, Antwerp, Belgium.

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Table 1: Included studies

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Author Patient Population N Mean age Questionnaire Clinimetric Outcome

Country Setting (%male)

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Moss-Morris (2002) RA 76 59,0 (24%) IPQ-R (English) Test-retest reliability (RA) - Pearson's correlations

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New Zealand hospital outpatient clinics 53,9 (41%) PANAS Construct validity: Known group method (acute vs chronic) -

Chronic pain (> 3months) 63 Ambulatory Index independent samples t-test

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hospital based chronic 35,7 (57%) SIP

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pain clinics Fatigue Severity Scale

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Acute pain (< 6 weeks) 35

private PT practice

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Van Ittersum (2009) FM 196 49 (12%) IPQ-R-FM (Dutch) Internal consistency - Cronbach's α

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The Netherlands PT treatment centre VAS Construct validity: structural validity - MGM (CFA)
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IPQ-R (English)

Van Wilgen (2008) FM 51 44 (8%) IPQ-R-FM (Dutch) Internal consistency - Cronbach's α

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The Netherlands Dutch FM patient association with 8 FM specific causes Test-retest reliability - Pearson's correlations
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FIQ Construct validity: hypotheses testing: Correlation with catastrophizing

PCS Pearson's correlations

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Albert (2013) Musculoskeletal disorder 43 41 (46,5%) IPQ-R-WD (French) Internal consistency - Cronbach's alpha

Canada with absence from work -> with new items Construct validity: hypotheses testing - multiple regression analyses

3m-1y TSK and Pearson correlation

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PCS

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PDI-14

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PDI

SERWS

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Pain beliefs and

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perceptions inventory

Implicit models of illness

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questionnaire

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VAS

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Chan (2009) Acute (1) hand injury, 57 38,2 (21%) IPQ-R-injury version Internal consistency - Cronbach's alpha

Ireland surgery required DASH Construct validity: hypotheses testing: Correlation with objective
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hospital HISS severity and subjective disability - Pearson
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Nicholls (2013) Knee pain (OA) 393 63,5 (38%) IPQ-R Construct validity: structural validity:
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UK Hand pain 2113 65,4 (37%) CFA (5 domains) - Goodness of fit - Chi², goodness of fit

Non-specific LBP 1591 43,9 (41%) index, Parsimony adjusted GFI, comparative fit index, RMSEA

EFA (causes) - PCA with varimax rotation

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Glattacker (2009) Orthopaedic 45 45,5 (33,3%) IPQ-R (German) Test-retest reliability - ICC, Pearson correlation coefficient

Germany 2 rehabilitation clinics HADS-D

Hallegraeff (2013) Acute non-specific LBP 84 42 (43%) Brief IPQ (Dutch) Internal consistency - Cronbach's alpha

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The Netherlands < 6 weeks SF36 Health Survey Test-Retest reliability - ICC

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physical therapy providers Measurement error - Limits of agreement, Bland Altman Plot

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Criterion validity: Concurrent validity (Mental Health component of

SF-36) - ICC and Pearson correlations

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Legend: OA = osteoarthritis, RA = rheumatoid arthritis, FM = fibromyalgia

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SIP = sickness impact profile, PANAS = Positive affect and negative affect scale, VAS = visual analogue scale, FIQ = fibromyalgia impact questionnaire, PCS = pain catastrophizing

scale, TSK = Tampa scale of kinesiophobia, PDI = pain disability index, PDI-14 = psychological distress index, SERWS = self-efficacy with regard to work capacity, DASH = disabilities

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of the arm, shoulder and hand, HISS = Hand injury severity score, HADS = Hospital Anxiety and Depression Scale, SF36 Health Survey = Short Form 36 Health Survey

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MGM = multiple group method, CFA = confirmatory factor analysis, EFA = exploratory factor analysis, RMSEA = root mean square error of approximation, ICC = intraclass correlation,

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PCA = principal component analysis
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Table 2: Assessment of methodological quality

Author COSMIN box Agreement Clinimetric Outcome Lowest score

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Moss-Morris (2002) E 5/6 Construct validity: Structural validity: known group method (acute vs chronic) - independent samples t-test Fair

B 10/11 Test-retest reliability (RA) - Pearson's correlations Fair

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Van Ittersum A 9/9 Internal consistency - Cronbach's α Good

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(2009) E 6/6 Construct validity: structural validity - CFA (MGM) Good

Van Wilgen (2008) A 8/9 Internal consistency - Cronbach's α Fair

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B 9/11 Test-retest reliability - Pearson's correlations Fair

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F 10/10 Construct validity: Hypotheses testing: Correlation with catastrophizing - Pearson's correlations Fair

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Albert (2013) A 9/9 Internal consistency - Cronbach's alpha Fair

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F 10/10 Construct validity: hypotheses testing - Pearson correlation matrix, multiple regression analysis Fair

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Chan (2009) A 9/9 Internal consistency - Cronbach's alpha Poor

F 10/10 Construct validity: Hypotheses testing: Correlation with objective severity and subjective Fair
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disability - Pearson

Nicholls (2013) E 6/6 Construct validity: Structural validity: Good

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CFA (5 domains) - Goodness of fit - Chi², goodness of fit index, Parsimony adjusted GFI,

comparative fit index, RMSEA

EFA (causes) - PCA with varimax rotation

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Glattacker (2009) B 9/11 Test-retest reliability (Orth) - ICC, Pearson correlation coefficient Fair

Hallegraeff (2013) A 6/9 Internal consistency - Cronbach's alpha Poor

B 5/11 Test-Retest reliability - ICC Fair

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C 5/11 Measurement error - Limits of agreement, Bland Altman Plot Fair

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H 3/6 Criterion validity: Concurrent validity (Mental Health component of SF-36) - ICC and Pearson Poor

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correlations

Legend: MGM= multigroup method, CFA = Confirmatory factor analysis, EFA = exploratory factor analysis, PCA = principal component analysis, GFI = goodness of fit index,

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CFI = comparative fit index, RMSEA = root mean square error of approximation, ICC = intraclass correlation, Orth = orthopaedic, RA= rheumatoid arthritis

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A= internal reliability, B= reliability, C= measurement error, D= content validity, E=structural validity, F=hypotheses testing, G=cross cultural validity, H=criterion validity

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Table 3: Adaptations of the IPQ-R in the included studies

Author (Year) "My illness" Illness identity Beliefs domain Causes Total

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Questionnaire was changed into…

Moss-Morris (2002) / 14 50° 18 70

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IPQ-R (English) 38°°

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Van Ittersum (2009) My fibromyalgia 14 37 18 69

IPQ-R-FM (Dutch)

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Van Wilgen (2008) My fibromyalgia 14 37 26 77

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IPQ-R-FM (Dutch)

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Albert (2013) My current health 16* 52** 20*** 88

IPQ-R-WD (French) condition

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Chan (2009) My injury 14 38 18 70

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IPQ-R-injury version
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Nicholls (2013) My hand/knee/back / / / /

IPQ-R (English) pain or problem

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Glattacker 2009 / 14 32 18 64
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IPQ-R (German)

Hallegraeff (2013) My low back pain / / / 8

Brief IPQ (Dutch)

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Legend: ° items in the first principle components analysis, °° remaining items

* 5 items removed, 7 added ** 26 new items added ***3 items removed, 5 added

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Table 4: Internal consistency and test-retest reliability of the IPQ-R

Internal consistency Test-retest reliability

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Cronbach's alpha Pearson correlations ICC
IPQ-R-
IPQ-R WD IPQ-R

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adapted
Van Van Albert et al. Moss- Van Glattacker et

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Ittersum Wilgen 2013 Morris et Wilgen et al.
et al. et al. al. al. 2009
2009 2008 2002 2008

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FM, FM, work disability 6 months, 3 weeks, 4 days,
n=196 n=51 due to MSD, RA FM Orth

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n=43
Illness . 57*** .24 .66 .66
Identity Identity / / / /
identity

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Timeline .55** .69** .87 .87
0.75 0.77 0.58 0.58
cyclical
Timeline
Timeline .35** .77** .66 .65

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0.80 0.80 0.81 0.81
acute/chronic

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Consequences Consequences 0.77 0.64 0.59 0.77 .74*** .75** .72 .71
Personal .57*** .57** .71 .69
Beliefs 0.77 0.83 0.59 0.68
control
domain
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Control/cure
Treatment .50*** .72** / /
0.79 0.67 0.73 0.77
control
Emotional Emotional .81*** .72** .78 .78
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0.81 0.86 0.81 0.87

representations representations
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Illness Illness .53*** .55** .56 .55

0.79 0.51 0.80 0.83
coherence coherence
Psychological 0.82*** .85**
0.82 0.90
attribution
Causes
Causes 0.72*** .69**
domain Risk factors 0.55 0.48
Immunity 0.62 0.47 0.58*** .73**
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Accident or 0.00- 0.53*** .62**

0.14
chance 0.61

Legend: IPQ-R-WD = Illness Perception Questionnaire Revised Work Disability, FM = fibromyalgia, MSD =
Musculoskeletal disorder, RA = rheumatoid arthritis, Orth = orthopaedics. ICC = intaclass coefficient. **p<0.01, ***p<0.001

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Table 5: Results of hypothesis testing for construct validity of the IPQ-R

Article and population Questionnaires Relationship with Results

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Van Wilgen (2008) IPQ-R-FM (Dutch) catastrophizing - Catastrophizing related to a low

FM FIQ
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(Pearson's correlations) understanding of the symptoms and positively
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PCS related to the more cyclical nature of FM and

an emotional representation
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- Anxiety was related to experiencing more

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consequences of FM, to an emotional

representation of FM, and to more

psychological attributions and more FM-

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specific attributions.

- Feeling depressed was related to a low score

for illness coherence, an emotional

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representation and more psychological

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attributions

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Chan (2009) IPQ-R-injury version objective severity and No significant correlation between

Acute hand injury, DASH subjective disability DASH/HISS scores and all the components of

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surgery required HISS (Pearson Product IPQ-R

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Moment Correlations)

Albert (2013) IPQ-R-WD (French) Convergent validity Adjusted r² between .33 and .70 (p≤.001)

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musculoskeletal disorder -> with new items (multiple regression Moderate to strong correlations for each

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with absence from work TSK analyses and Pearson dimension with six theoretically-related

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3m-1y PCS correlation) variables: TSK, PCS, PDI, PDI-14, PBPI,

PDI-14 IMIQ
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PDI No significant relation with VAS or SERWS
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SERWS
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PBPI

IMIQ

VAS
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SERWS = self-efficacy with regard to work capacity, VAS = visual analogue scale, DASH = disabilities of the arm,

shoulder and hand, HISS = Hand injury severity score, TSK = Tampa scale for kinesiophobia, PCS = pain catastrophizing

scale, PDI = pain disability index, IMIQ = Implicit models of illness questionnaire, PDI-14 = psychological distress index,

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PBPI = pain beliefs and perceptions inventory

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Table 6: Results of factor analysis for construct validity of the IPQ-R

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Article Dimension

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n Method Result
Patient population (number of items)

Van Ittersum (2009) 196 CFA MGM Beliefs domain (38) 7 factor-model: -> 55% of the variance
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FM Causal (18) 4 factor- model: -> 50% of the variance
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Nicholls (2013) CFA Goodness of fit - Beliefs domain (38) 7 factor-model: goodness-of-fit statistics
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knee pain (OA) 330 Chi², GFI, were below the criteria

hand problem 1621 Parsimony adjusted

acute non-specific LBP 1319 GFI, CFI, RMSEA

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EFA PCA varimax Causal (18) Knee: 5 factors -> 62% of the variance

rotation Hand: 4 factors -> 56% of the variance

LBP: 3 factors -> 51% of the variance

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Legend: CFA = Confirmatory factor analysis, EFA = exploratory factor analysis, MGM = multigroup method, PCA = principal

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component analysis, GFI = goodness of fit index, CFI = comparative fit index, RMSEA = root mean square error of

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approximation, OA = osteoarthritis, LBP = low back pain

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Figure 1: Flowchart of the selection process

75 records identified 2 additional records

Identification

through database searching identified through other

sources

65 records excluded
77 records screened

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- Population: 36
- Intervention: 8
Screening

- Outcome: 12
- Design: 7

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- Language: 2
Eligibility

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12 full-text articles 4 full-text articles excluded
assessed for eligibility - No full text available: 3
- Outcome: 1

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Included

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8 studies included in
systematic review
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