* Corresponding author. Address: Centre for Interdisciplinary Research in Rehabilitation and Social Integration, Quebec Rehabilitation Institute, 525, Boulevard Wilfrid Hamel, Quebec City, QC G1M 2S8, Canada. Tel.: 418-907-5858. E-mail address: ac.lavalu@1.ebud.reivilo-cram (M.-O. Dubé).
Received 2021 May 10; Revised 2021 Sep 13; Accepted 2021 Sep 29.Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain.
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The Pain Self-Efficacy Questionnaire has excellent validity, reliability, and responsiveness. Further high-quality studies are needed to determine responsiveness in populations other than chronic low back pain.
Keywords: Pain self-efficacy, Pain, Musculoskeletal, PSEQ, MeasurementA higher level of pain self-efficacy has been suggested as a predictor of a better outcome in patients with musculoskeletal disorders. The Pain Self-Efficacy Questionnaire (PSEQ) is one of the most frequently used patient-reported outcome measures for pain self-efficacy. The purpose of this study was to conduct a systematic review that would identify, appraise, and synthetize the psychometric properties of the PSEQ. Embase, MEDLINE, and CINAHL databases were searched for publications reporting on psychometric properties of the PSEQ in populations with musculoskeletal disorders. After applying selection criteria on identified citations, 28 studies (9853 participants) were included. The methodological quality as measured with the COSMIN risk of bias tool varied from adequate to very good for most measurement properties. The results showed a weighted mean intraclass correlation coefficient of 0.86 (range: 0.75–0.93) for test–retest reliability for the original 10-item PSEQ and the minimal detectable change at 95% confidence interval was 11.52 out of 60 points. Effect size and standardized response mean values were 0.53 and 0.63, respectively, whereas the minimal clinically important difference ranged from 5.5 to 8.5 in patients with chronic low back pain. Internal consistency (Cronbach alpha) ranged from 0.79 to 0.95. The results also showed that the PSEQ has low to moderate correlations with measures of quality of life, disability, pain, pain interference, anxiety, depression, and catastrophizing. Finally, the PSEQ has been adapted and validated in 14 languages. Overall, the results demonstrate that the PSEQ has excellent validity, reliability, and responsiveness. Further high-quality studies are needed to determine responsiveness in populations other than chronic low back pain.
Keywords: Pain self-efficacy, Pain, Musculoskeletal, PSEQ, MeasurementOne in 3 people live with chronic musculoskeletal (MSK) disorders. 12 Musculoskeletal disorders can lead to decreased participation and quality of life as well as increased all-cause mortality. 11 Many factors have been studied to better understand the persistence of MSK pain over time; pain self-efficacy being one of them. 28 Self-efficacy was originally defined as an individual's confidence or belief in their capacity to achieve goals or perform activities. 4 More specifically in the MSK field, pain self-efficacy is defined as the confidence that one has to perform their activities and achieve their goals despite the presence of symptoms or pain. 35 A higher level of pain self-efficacy has been suggested as a predictor of a better prognosis in those with MSK pain 28 and has been associated with less disability, pain, fatigue, and emotional distress. 27
Several scales have been developed to measure pain-related self-efficacy, namely, the Arthritis Self-Efficacy Scale (ASES; 20 items), the Chronic Disease Self-Efficacy Scale (33 items), the Pain Self-Efficacy Questionnaire (PSEQ; 10 items), the Chronic Pain Self-Efficacy Scale (22 items), and the Self-Efficacy Scale (8 items). 32,47 The number of items in these scales varies from 8 to 33 items, leading to a variable response burden (completion times). 47 Among all self-efficacy questionnaires, the PSEQ is the most frequently used in clinical setting for MSK disorders. 15,36,47 According to a Delphi study, it is the preferred clinician tool to assess pain-related self-efficacy. 39 It is a short self-administered questionnaire that has been extensively studied with various MSK disorders 10,20,26 and translated in many languages. 2,25,37,38
Only 1 systematic review has been published on the psychometric properties of assessment tools for pain self-efficacy. 47 This systematic review included all available pain self-efficacy scales for a population with low back pain (LBP). The main findings were that the PSEQ and Chronic Pain Self-Efficacy Scale were the most commonly studied scales and that internal consistency was reported in all original included studies but other measurement properties such as reliability, validity, and responsiveness were poorly reported. In that systematic review, methodology for data extraction was not described and authors did not perform a quality assessment of included studies to evaluate the risk of bias of included studies. This lack of methodological evaluation and description in the review process limits the ability to conclude on the psychometric properties of the evaluated outcome measures.
Currently, no evidence synthesis or systematic review on the measurement properties of the PSEQ, the most widely used pain self-efficacy questionnaire, has been published for MSK disorders. To use this questionnaire in research and clinical contexts, it is important to review and assess the quality of evidence evaluating its measurement properties. The purpose of this study was to conduct a systematic review that would identify, appraise, and synthetize the psychometric properties of the PSEQ.
The PSEQ is a 10-item questionnaire, originally developed in English, aimed to assess the confidence of people with persistent pain to achieve different activities despite their pain. 35 Each item is rated by selecting a number on a 7-point numerical scale (scores from 0 to 6), where 0 means “not at all confident” and 6 means “completely confident.” It can be used with different populations of people with persistent pain. 19,20,35 Items cover functions such as work, social activities, household chores, and coping with pain without medication. A total score is calculated by summing the scores for each of the 10 items, yielding a total score ranging from 0 to 60. Higher scores reflect stronger self-efficacy beliefs. 35 Shorter versions (PSEQ-2 and PSEQ-4) including 2 and 4 items, respectively, have also been developed. 1,8,10,31 Refer to Table Table1 1 for a list of the PSEQ Items.
| Items |
|---|
| 1. I can enjoy things, despite the pain. |
| 2. I can do most of the household chores (tidying up, washing dishes, etc), despite the pain. |
| 3. I can socialize with my friends or family members as often as I used to do, despite the pain. |
| 4. I can cope with my pain in most situations. |
| 5. I can do some form of work, despite the pain. (“work” includes housework, paid, and unpaid work). |
| 6. I can still do many of the things I enjoy doing, such as hobbies or leisure activity, despite pain. |
| 7. I can cope with my pain without medications. |
| 8. I can still accomplish most of my goals in life, despite the pain. |
| 9. I can live in a normal lifestyle, despite the pain. |
| 10. I can gradually become more active, despite the pain. |
PSEQ, Pain Self-Efficacy Questionnaire.
A database search using Embase, MEDLINE, and CINAHL was performed January 29, 2021, by a librarian from Université Laval. The following keywords were used to search databases for eligible studies: Pain Self-Efficacy Questionnaire, PSEQ, PSEQ-10, PSEQ-2, PSEQ-4, Reliability, Reproducibility, Validity, Validation, Responsiveness, Translation, Minimal detectable change, MDC, minimal clinical important difference, MCID, Factor analysis, Rasch, Internal coherence, Internal consistency, Psychometric properties, and Measurement properties. Keywords related to the population of interest were not included for the databases search because the PSEQ was originally developed to be used in a population with chronic pain. 35 Complete search strategy, MeSH, and keywords are available in Appendix 1. Hand searches of retrieved study reference lists were also conducted.
Covidence software was used for the selection phase of the study. The titles and abstracts of each article were first independently reviewed by 2 of the authors, and an article was accepted for a full review if it met the following inclusion criteria: (1) original studies that aim to report at least one of the validity and/or reliability indices of the PSEQ-10 or one of its shortened versions, (2) written in English or French, and (3) included adult population with any MSK disorder. Articles were excluded if any of the following were retrieved: (1) studies reporting the psychometric properties of the PSEQ in nonmusculoskeletal disorders and (2) systematic reviews, narrative reviews, scoping reviews, meta-analyses, study protocols, or conference proceedings. A consensus between 2 authors was needed to include an article.
A pair of raters independently reviewed each article that met the inclusion criteria. The COnsensus-based Standards for the selection of health Measurement INstruments (COSMIN) quality appraisal tool was used to appraise the quality of measurement properties described in included studies. 33 The COSMIN quality appraisal tool recommends rating the quality of each measurement property reported in each included study. Measurement properties were rated, when applicable, according to the following categories: (1) patient-reported outcome measure development, (2) content validity, (3) structural validity, (4) internal consistency, (5) cross-cultural validity or measurement invariance, (6) reliability, (7) measurement error, (8) criterion validity, (9) construct validity, and (10) responsiveness. Each category contains a series of items related to the specific measurement properties. Each item was rated as “very good,” “adequate,” “doubtful,” or “inadequate” by assessing the information reported in the study being evaluated. 33 The lowest score among all items was then used to rate the quality of each measurement property evaluated for every individual study. 44 All the authors first met for a calibration review, where they independently reviewed 3 articles and then discussed each item to clarify the meaning and interpretation of critical appraisal items. Then, the pair of raters independently evaluated an assigned subset of articles. A consensus meeting was held to produce a consensus statement on each rated property of every included study. The Gwet AC2 coefficient (quadratic weights) was used to evaluate the preconsensus agreement on the COSMIN scores between the 2 reviewers. 49
A standardized data extraction form used in previous systematic reviews 9,40 was used to extract data from included studies. Information on the patient population of each study was extracted, including the number of participants, medical conditions, age, sex, and intervention provided when applicable. The following psychometric properties were also extracted: reliability (test–retest intraclass correlation coefficient [ICC], SEM, minimal detectable change [MDC], and internal consistency), validity (content, construct, factorial, known-group, and floor/ceiling effects), responsiveness (effect size [ES], standardized response mean [SRM], and minimal clinically important difference [MCID]), time to administer, and cross-cultural adaptation. One reviewer extracted the data, and a second reviewer verified the transcription to reduce risk of error. Overall relative and absolute reliability (ICC, SEM, and MDC) and responsiveness (ES and SRM) were pooled and determined by calculating a weighted average over all studies (weighted by sample size). Intraclass correlation coefficient were considered excellent if higher than 0.81, good from 0.61 to 0.80, moderate from 0.41 to 0.60, fair from 0.21 to 0.40 and poor if less than 0.20. 41 Effect size and SRM were considered large if higher than 0.8, moderate between 0.50 and 0.80, and small between 0.20 and 0.50. 18 Pearson or Spearman correlations were categorized as high if higher than 0.70, moderate between 0.50 and 0.70, low between 0.26 and 0.49, and very low between 0.01 and 0.25. 34 For construct validity, the following 3 hypotheses were formulated, and data were extracted to confirm or infirm those hypotheses. First, correlation would be positive and moderate to high (r > 0.50) between PSEQ-10 and shortened versions of the PSEQ. Second, positive and moderate correlations (0.50 < r < 0.70) between self-efficacy and quality of life were expected. Third, negative low to moderate correlations (−0.26 < r < −0.70) between self-efficacy and pain, pain interference, anxiety, depression, catastrophizing, and disability were expected. The second and third hypotheses are in line with the original development study of the PSEQ-10. 35
The PRISMA study selection flowchart is presented in Figure Figure1. 1 . The literature search revealed a total of 347 citations. After removal of duplicates, the inclusion and exclusion criteria were applied by screening titles and abstracts of 111 studies. Thirty-four full-text studies were then screened for eligibility. Of these 34 studies, 5 were excluded because of their targeted outcome measure (2 studies), patient population (2 studies), or study design (1 study). Another study was excluded because it was a conference proceeding (abstract only). Therefore, 28 studies 1–3,7,8,10,13–17,19–23,25,26,29,31,35–38,45,46,48,50 were included, in which a total of 9853 participants were involved.
PRISMA flow diagram.
The detailed characteristics of included studies can be found in Table Table2. 2 . While 22 included studies evaluated several psychometric properties of the PSEQ-10, 6 studies 1,10,16,31,36,50 evaluated the psychometric properties of either one or both of its short forms, namely, the PSEQ-2 (evaluated in the 6 studies) and the PSEQ-4 (evaluated in 3 of these 6 studies). Populations evaluated in included studies comprised chronic LBP, 14,17,20,21,29,50 fibromyalgia, 37 neck pain, 15 upper limb MSK pain, 8,10,23 knee osteoarthritis, 26 and any chronic MSK disorder. 1–3,8,10,13,16,19,22,25,31,35,36,38,45,46,48
Characteristics of included studies.
| Study ID | Questionnaire | Population | Properties evaluated | |||
|---|---|---|---|---|---|---|
| Disorders | Total, n | Mean age (SD) | Gender (% F) | |||
| Adachi et al., 2014 2 | PSEQ-10/Japanese | Chronic MSK pain | 176 | 64.33 (15.12) | 54.5% | Test–retest reliability Internal consistency Factorial validity Construct validity Predictive validity Cross-cultural/language translation |
| Adachi et al., 2019 1 | PSEQ-10, PSEQ-2, and PSEQ-4/Japanese | Chronic MSK pain | 150 | 54.75 (15.73) | 63% | Internal consistency Factorial validity Construct validity |
| Asghari et al., 2009 3 | PSEQ-10/Persian | Chronic MSK pain | 517 | 40.6 (14.1) | 39.5% | Test–retest reliability Internal consistency Factorial validity Construct validity Cross-cultural/language translation |
| Bot et al., 2013 7 | PSEQ-10/Web based | Upper limb MSK pain | 99 | 49 (18) | 46% | Construct validity |
| Bot et al., 2014 8 | PSEQ-10 and PSEQ-2 | Upper limb MSK pain | 316 | 46 (16) | 47% | Internal consistency Content validity Construct validity |
| Briet et al., 2014 10 | PSEQ-10 and PSEQ-2 | Upper limb MSK pain | 249 | 47 (16) | 54% | Test–retest reliability Measurement error Internal consistency Floor/ceiling effect Construct validity |
| Castarlenas et al., 2020 13 | PSEQ-10/Catalan | Chronic MSK pain | 227 | 17.87 (3.08) | 70% | Internal consistency Factorial validity Construct validity Cross-cultural/language translation |
| Chala et al., 2021 14 | PSEQ-10/Amharic | Chronic low back pain | 240 | 40.93 (13.5) | 59.2% | Test–retest reliability Measurement error Internal consistency Floor/ceiling effect Factorial validity Construct validity Cross-cultural/language translation |
| Chiarotto et al., 2014 17 | PSEQ-10/Italian | Chronic low back pain | 165 | 49.9 (12.4) | 64.8% | Test–retest reliability Measurement error Internal consistency Floor/ceiling effect Factorial validity Construct validity Cross-cultural/language translation |
| Chiarotto et al., 2016 16 | PSEQ-10, PSEQ-2, and PSEQ-4/Italian | Chronic low back pain | 104 | 48.85 (12.23) | 68% | Responsiveness |
| Chiarotto et al., 2018 15 | PSEQ-10/Italian | Subacute and chronic neck pain | 161 | 44.55 (15.81) | 65% | Factorial validity Internal consistency Construct validity Responsiveness |
| Costa et al., 2016 19 | PSEQ-10 | Chronic MSK pain | 1511 | 48.9 (16.1) | 57% | Content validity Factorial validity |
| DiPietro et al., 2014 20 | PSEQ-10 | Subacute and chronic low back pain | 610 | 48.1 (15.1) | 50.7% | Internal consistency Floor/ceiling effect Factorial validity Construct validity |
| Fatoye et al., 2021 21 | PSEQ-10/Yoruba | Chronic low back pain | 131 | 51.92 (16.1) | 50.4% | Test–retest reliability Measurement error Internal consistency Floor/ceiling effect Construct validity Cross-cultural/language translation |
| Ferreira-Vallente et al., 2011 22 | PSEQ-10/Portuguese (European) | Chronic MSK pain | 174 | 59.18 (16.11) | 59.2% | Measurement error Internal consistency Construct validity Cross-cultural/language translation |
| Kortlever et al., 2015 23 | PSEQ-10 | Upper limb MSK pain | 134 | 52 (Median); 35–64 (IQR) | 57% | Internal consistency Floor/ceiling effect Factorial validity Construct validity |
| Lim et al., 2007 25 | PSEQ-10/Chinese | Chronic MSK pain | 120 | 40 (9.6) | 58.3% | Test–retest reliability Internal consistency Factorial validity Construct validity Cross-cultural/language translation |
| Lincoln et al., 2017 26 | PSEQ-10 | Knee osteoarthritis | 192 | 67 (10) | 53% | Content validity |
| Maughan et al., 2010 29 | PSEQ-10 | Chronic low back pain | 48 | 52 | 67% | Test–retest reliability Measurement error Responsiveness |
| McWilliams et al., 2015 31 | PSEQ-10 and PSEQ-4 | Chronic MSK pain | 280 | 47.9 (10.1) | 66.1% | Internal consistency Construct validity |
| Nicholas et al., 2007 35 | PSEQ-10 | Chronic MSK pain | 1554 | 41 | NR | Test–retest reliability Internal consistency Factorial validity Content validity Construct validity |
| Nicholas et al., 2015 36 | PSEQ-10; PSEQ-2 | Chronic MSK pain | 1558 | 48.8 (16.1) | 51.5% | Test–retest reliability Internal consistency Construct validity Responsiveness |
| Rasmussen et al., 2015 37 | PSEQ-10/Danish | Fibromyalgia | 99 | 46.5 | 94% | Test–retest reliability Internal consistency Floor/ceiling effect Content validity Factorial validity Construct validity Cross-cultural/language translation |
| Sarda et al., 2007 38 | PSEQ-10/Portuguese (Brazilian) | Chronic MSK pain | 311 | 48.9 (14.06) | 74% | Internal consistency Factorial validity Construct validity Cross-cultural/language translation |
| Tuck et al., 2020 45 | PSEQ-10/Mongolian | Chronic MSK pain | 142 | 53.96 (15.50) | 61% | Internal consistency Construct validity Cross-cultural/language translation |
| Ugwuanyi et al., 2020 46 | PSEQ-10/Nigerian | Chronic MSK pain | 256 | NR | NR | Test–retest reliability Internal consistency Factorial validity |
| Vong et al., 2009 48 | PSEQ-10/Chinese | Chronic MSK pain | 120 | 41.9 (12.21) | 67.5% | Internal consistency Factorial validity Construct validity |
| Yang et al., 2019 50 | PSEQ-10 and PSEQ-2/Chinese (Mainland) | Chronic low back pain | 219 | 53.4 (11.5) | 42.9% | Test–retest reliability Internal consistency Factorial validity Construct validity Cross-cultural/language translation |
Table Table3 3 presents the quality of properties evaluated by the COSMIN risk of bias tool. The risk of bias assessment demonstrated a good overall preconsensus agreement between the 2 reviewers (Gwet AC2 coefficient = 0.62; P < 0.00001; observed agreement = 84.96%; agreement by chance = 60.39%). The overall quality of the PSEQ development study 35 and the content validity were rated as doubtful mainly because the methods used to assess the comprehensibility and comprehensiveness of the PSEQ were poorly described. Overall, structural validity, internal consistency, cross-cultural validity, construct validity, and responsiveness designs were of very good quality in most of the included studies (75 of 79 [94.9%] measurement properties rated). For test–retest reliability and measurement error, failure to document (1) if patients were stable between 2 measurement time points, (2) the time interval between the 2 tests, or (3) similarity of the 2 measurements conditions resulted in 3 of 13 studies (23.1%) obtaining an inadequate score, 4 of 13 studies (30.8%) obtaining a doubtful score, and 4 of 13 studies (30.8%) obtaining an adequate score.
COSMIN risk of bias of included studies.
| Study | 1a. | 1b. | 2.a | 2.b | 2.c | 2.d | 2.e | 3. | 4. | 5. | 6. | 7. | 8. | 9a | 9b | 10a | 10b | 10c | 10d |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Nicholas et al., 2007 35 | D | D | — | — | D | — | — | — | V | — | I | — | — | V | — | — | — | — | — |
| Lim et al., 2007 25 | — | — | — | — | — | — | — | A | V | V | D | — | — | V | — | — | — | — | — |
| Sarda et al., 2007 38 | — | — | — | — | — | — | — | V | V | — | — | — | — | V | — | — | — | — | — |
| Asghari et al., 2009 3 | — | — | — | — | — | — | — | V | V | V | V | — | — | V | — | — | — | — | — |
| Vong et al., 200948 | — | — | — | — | — | — | — | V | V | — | — | — | — | V | — | — | — | — | — |
| Ferreira-Vallente et al., 2011 22 | — | — | — | — | — | — | — | — | V | V | — | — | — | V | — | — | — | — | — |
| Bot et al., 2013 7 | — | — | — | — | — | — | — | — | — | — | — | — | — | V | — | — | — | — | — |
| Bot et al., 2014 8 | — | — | — | — | — | — | — | — | V | — | — | — | — | — | — | — | — | — | — |
| Adachi et al., 2014 2 | — | — | — | — | — | — | — | — | V | V | D | — | V | V | — | — | — | — | — |
| Briet et al., 2014 10 | — | — | — | — | — | — | — | — | V | — | I | I | — | V | — | — | — | — | — |
| Chiarotto et al., 2014 17 | — | — | — | — | — | — | — | V | V | V | A | A | — | V | — | — | — | — | — |
| Di Pietro et al., 2014 20 | — | — | — | — | — | — | — | — | V | — | — | — | — | V | — | — | — | — | — |
| McWilliams et al., 2015 31 | — | — | — | — | — | — | — | — | V | — | — | — | — | V | — | — | — | — | V |
| Nicholas et al., 2015 36 | — | — | — | — | — | — | — | — | V | — | A | — | I | V | — | — | — | — | I |
| Kortlever et al., 2015 23 | — | — | — | — | — | — | — | A | V | — | — | — | — | V | — | — | — | — | — |
| Rasmussen et al., 2015 37 | — | — | — | — | — | — | — | V | V | V | V | — | — | — | — | — | — | — | — |
| Chiarotto et al., 2016 16 | — | — | — | — | — | — | — | — | — | — | — | — | — | — | — | V | V | — | V |
| Costa et al., 2016 19 | — | — | — | — | — | — | — | V | — | — | — | — | — | — | — | — | — | — | — |
| Lincoln et al., 2017 26 | — | — | — | — | — | — | — | V | — | — | — | — | — | — | — | — | — | — | — |
| Chiarotto et al., 2018 15 | — | — | — | — | — | — | — | V | V | — | — | — | — | V | — | — | V | V | V |
| Adachi et al., 2019 1 | — | — | — | — | — | — | — | — | V | — | — | — | I | V | — | — | — | — | — |
| Maughan et al., 2010 29 | — | — | — | — | — | — | — | — | — | — | D | D | — | — | — | — | — | — | V |
| Yang et al., 2019 50 | — | — | — | — | — | — | — | V | V | V | A | — | I | V | — | — | — | — | — |
| Castarlenas et al., 2020 13 | — | — | — | — | — | — | — | V | V | V | — | — | — | V | — | — | — | — | — |
| Tuck et al., 2020 45 | — | — | — | — | — | — | — | V | V | V | — | — | — | V | — | — | — | — | — |
| Uguwani et al., 2020 46 | — | — | — | — | — | — | — | I | V | — | I | — | — | — | — | — | — | — | — |
| Chala et al., 2021 14 | — | — | — | — | — | — | — | V | V | V | A | — | — | V | — | — | — | — | — |
| Fatoye et al., 2021 21 | — | — | — | — | — | — | — | — | V | V | D | D | — | V | — | — | — | — | — |
The COSMIN quality of the PSEQ development study (Box 1) and content validity (Box 2) were judged as doubtful, mainly because there was not enough description of the qualitative process used to develop the PSEQ, neither from a patient nor from a clinician perspective. Nicholas 35 developed the original English version of the PSEQ, namely, the PSEQ-10 (development study published in 2007). The 10 items were selected from other questionnaires and from the authors' clinical experience. The content validity was then tested on 85 patients using a qualitative testing analysis of a patient's comprehensibility of the questionnaire. A confirmatory factor analysis then showed that the questionnaire was unidimensional with a corrected item-total correlation that varied from 0.67 to 0.84 when used in a population with chronic LBP. 35 The 1-dimensionality of the PSEQ-10 was confirmed in 16 other studies in populations with chronic MSK pain, neck pain, and upper limb MSK pain. 2,3,13–15,17,20,23,25,26,37,38,45,46,48,50 Regarding the COSMIN quality score for structural validity, 12 studies were rated as very good, 2,3,13–15,17,20,26,37,38,45,48,50 2 as adequate, 23,25 and 1 as inadequate. 46 All items of the questionnaire performed well overall on factorial analysis except for item 7 of the questionnaire, “I can cope with my pain without medication,” which performed constantly worse on item fit analysis than other items but was deemed clinically relevant by authors. 17,19,20,35,38 Two versions of the PSEQ-2 were developed. One version consisted of items 8 and 9 8 and another version consisted of items 5 and 9 (refer to Table Table1 1 for specific item wording). 36 The structural validity of both versions of the PSEQ-2 was confirmed (1 dimension) in 3 studies with a moderate to high corrected item- total correlation. 1,7,31 Finally, the PSEQ-4 consisted of items 4, 6, 8, and 9, and its structural validity was also confirmed (1 dimension). 31
Floor and ceiling effects were examined in several language versions of the PSEQ-10. The English version showed no floor effect and a ceiling effect that ranged from 0% to 20%. 10,20,23 The Italian, 17 Danish, 37 and Yoruba 21 versions of the PSEQ-10 did not show ceiling or floor effects. The Amharic version did not show a floor effect but showed a minimal ceiling effect of 4.8%. 14 The PSEQ-2 (version with items 8 and 9) showed a minimal floor effect of 1.6% but a ceiling effect of 41.7% which means that PSEQ-2 does not allow to discriminate among those who have a higher level of pain self-efficacy. 10
Table Table4 4 summarizes findings for construct validity. Convergent and divergent validity of the PSEQ were assessed by calculating correlations (Pearson (r) or Spearman (Rho)) between PSEQ total scores and total scores of several other patient-reported outcome measures in 19 included studies. COSMIN risk of bias for construct validity was rated as very good for all 19 included studies that evaluated this measurement property. Quality of life evaluated by the SF-12 or SF-36 questionnaires showed low to moderate positive statistically significant correlations with the PSEQ-10 for chronic LBP or MSK pain (7 studies; 1277 participants; correlation range: 0.38–0.57). 2,3,14,22,25,48,50 For divergent validity, there was a low to moderate negative statistically significant correlation between function or disability (higher score = lower level of function/disability) (10 studies; 2630 participants; correlation range: −0.71 to −0.29), 3,7,10,15,17,31,36,38,48,50 pain interference (5 studies; 1526 participants; correlation range: −0.67 to −0.40), 2,36,38,45,50 anxiety (5 studies; 805 participants; correlation range: −0.63 to −0.32), 1,22,25,45,50 or depression (9 studies; 2276 participants; correlation range: −0.68 to −0.32) 1,3,17,22,25,31,36,45,50 and the PSEQ-10 or shortened forms of the PSEQ for chronic LBP, upper limb pain, or MSK pain. Correlations between the PSEQ and catastrophizing variables mainly measured by the Pain Catastrophizing Scale varied from low to high and were statistically significant among studies that included various populations with chronic MSK pain (10 studies, 3495 participants, correlation range: −0.74 to −0.36). 1,2,13,15,17,25,31,35,36,45 Correlation levels between pain intensity and PSEQ varied from very low to low (12 studies; 2087 participants, correlation range: −0.50 to −0.05) 1,7,10,15,17,21,22,25,31,38,45,48 with the Chinese 25 and Yoruba 21 versions that did not meet statistical significance. Thus, our original hypotheses formulated in the methodology section were confirmed. Finally, the hypothesis that the short version was correlated with the PSEQ-10 was also confirmed with a high statistically significant positive correlation between the PSEQ-10 and the PSEQ-2 for chronic MSK pain and for upper limb MSK pain (4 studies; 1318 participants; correlation range: 0.76–0.94). 1,8,36,50
Summary of findings for construct validity.
| Convergent validity with: | Correlation (high, moderate, low, and very low) | Person (r) or Spearman (Rho) correlation coefficient, significance, PSEQ version (other than PSEQ-10) when applicable, and population studied. |
|---|---|---|
| Original vs short version | ||
| PSEQ-10 vs PSEQ-2 | High | r = 0.94, P < 0.001 for chronic MSK pain 50 |
| High | r = 0.93, P < 0.001 for chronic MSK pain 36 | |
| High | r = 0.92, P < 0.001 for chronic MSK pain 1 | |
| High | r = 0.76, P < 0.001 for chronic upper limb MSK pain 8 | |
| Quality of life | ||
| SF-12 physical | Moderate | r = 0.52, P ≤ 0.001 for chronic MSK pain 3 |
| SF-12 physical | Moderate | r = 0.51, P < 0.01 for chronic MSK pain 22 |
| SF-12 mental | Low | r = 0.46, P < 0.01 for chronic MSK pain 22 |
| SF-12 mental | Low | r = 0.42, P ≤ 0.001 for chronic MSK pain 3 |
| SF-36 physical | Low | r = 0.43, P < 0.001 for chronic LBP 50 |
| SF-36 physical | Low | r = 0.41, P < 0.001 for chronic MSK pain 2 |
| SF-36 physical | Low | r = 0.40, P < 0.001 for chronic MSK pain 25 |
| SF-36 physical | Low | Rho = 0.38, P < 0.01 for chronic and acute LBP 14 |
| SF-36 physical | Low | r = 0.38, P < 0.001 for PSEQ-2 on chronic LBP 50 |
| SF-36 mental | Moderate | r = 0.57, P < 0.001 for chronic LBP 50 |
| SF-36 mental | Low | r = 0.47, P < 0.001 for PSEQ-2 on chronic LBP 50 |
| SF-36 mental | Low | r = 0.46, P < 0.001 for chronic MSK pain 48 |
| SF-36 mental | Low | r = 0.40, P < 0.001 for chronic MSK pain 2 |
| Pain intensity | ||
| VAS | Moderate | r = −0.50, P < 0.001 for chronic upper limb MSK pain 7 |
| VAS | Low | Rho = −0.46, P < 0.01 for chronic MSK pain 45 |
| VAS | Low | r = −0.45, P < 0.001 for chronic upper limb MSK pain 10 |
| VAS | Low | r = −0.40, P < 0.001 for chronic MSK pain 17 |
| VAS | Low | r = −0.38, P < 0.001 for PSEQ-2 on chronic upper limb MSK pain 10 |
| VAS | Low | r = −0.36, P < 0.001 for chronic MSK pain 1 |
| VAS | Low | r = −0.36, P < 0.001 for chronic MSK pain 49 |
| VAS | Low | r = −0.33, P < 0.001 for PSEQ-2 on chronic upper limb MSK pain 7 |
| VAS | Low | r = −0.29, P < 0.001 for chronic MSK pain 31 |
| VAS | Low | r = −0.28, P < 0.01 for chronic MSK pain 22 |
| VAS | Very low | r = −0.25, P ≤ 0.001 for chronic MSK pain 38 |
| VAS | Very low | r = −0.24, P < 0.001 for PSEQ-4 on chronic MSK pain 31 |
| VAS | Very low | r = −0.18, P < 0.001 for PSEQ-2 on chronic MSK pain 31 |
| VAS | Very low | r = −0.121, P = 0.189 for chronic MSK pain 25 |
| VAS | Very low | r = −0.05, P = 0.59 for chronic MSK pain 21 |
| NRS | Very low | Rho = −0.14 P < 0.05 for chronic neck pain 15 |
| Pain interference | ||
| BPI | Moderate | r = −0.67, P < 0.001 for chronic MSK pain 36 |
| BPI | Moderate | r = −0.64, P < 0.001 for PSEQ-2 on chronic MSK pain 36 |
| BPI | Moderate | Rho = −0.60, P < 0.01 for chronic MSK pain 45 |
| BPI | Moderate | r = −0.58, P ≤ 0.001 for chronic MSK pain 38 |
| BPI | Low | r = −0.43, P < 0.001 for chronic MSK pain 2 |
| BPI | Low | r = −0.42, P < 0.001 for PSEQ-2 on chronic LBP 50 |
| MPI | Low | r = −0.40, P < 0.001 for chronic LBP 50 |
| Function/disability | ||
| QuickDASh | High | r = −0.71, P < 0.001 for chronic upper limb MSK pain 10 |
| QuickDASH | High | r = −0.71, P < 0.001 for PSEQ-2 on chronic upper limb MSK pain 10 |
| QuickDASH | Moderate | r = −0.67, P < 0.001 for chronic upper limb MSK pain 7 |
| QuickDASH | Low | r = −0.44, P < 0.001 for PSEQ-2 on chronic upper limb MSK pain 7 |
| RMDQ | Moderate | r = −0.66, P < 0.001 for chronic MSK pain 17 |
| RMDQ | Moderate | r = −0.65, P < 0.001 for chronic MSK pain 49 |
| RMDQ | Moderate | r = −0.58, P < 0.001 for chronic MSK pain 38 |
| RMDQ | Moderate | r = −0.55, P < 0.001 for chronic MSK pain 36 |
| RMDQ | Moderate | r = −0.54, P < 0.001 for PSEQ-2 on chronic MSK pain 36 |
| RMDQ | Low | r = −0.43, P < 0.001 for PSEQ-2 on chronic LBP 50 |
| RMDQ | Low | r = −0.41, P < 0.001 for chronic LBP 50 |
| RMDQ | Low | r = −0.40, P < 0.001 for chronic MSK pain 3 |
| RMDQ | Low | r = −0.35, P < 0.001 for PSEQ-4 on chronic MSK pain 31 |
| RMDQ | Low | r = −0.29, P < 0.001 for PSEQ-2 on chronic MSK pain 31 |
| AVD-IASP-S | Low | r = −0.41, P < 0.001 for chronic MSK pain 31 |
| NDI | Low | Rho = −0.38 P < 0.05 for chronic neck pain 15 |
| Anxiety | ||
| HADS-A | Moderate | r = −0.63, P < 0.001 for PSEQ-2 on chronic LBP 50 |
| HADS-A | Moderate | r = −0.59, P < 0.001 for chronic LBP 50 |
| HADS-A | Moderate | r = −0.56, P < 0.001 for chronic MSK pain 25 |
| HADS-A | Moderate | r = −0.55, P < 0.001 for chronic MSK pain 1 |
| HADS-A | Low | r = −0.39, P < 0.01 for chronic MSK pain 22 |
| DASS-A | Low | Rho = −0.32, P < 0.01 for chronic MSK pain 45 |
| Depression | ||
| HADS-D | Moderate | r = −0.68, P < 0.001 for chronic MSK pain 1 |
| HADS-D | Moderate | r = −0.67, P < 0.001 for chronic LBP 50 |
| HADS-D | Moderate | r = −0.66, P < 0.001 for chronic MSK pain 25 |
| HADS-D | Moderate | r = −0.51, P < 0.01 for chronic MSK pain 22 |
| HADS-D | Low | r = −0.48, P < 0.001 for chronic MSK pain 3 |
| HADS-D | Low | r = −0.49, P < 0.001 for PSEQ-2 on chronic LBP 50 |
| HADS-D | Low | Rho = −0.45, P < 0.01 for chronic MSK pain 45 |
| HADS-D | Low | r = −0.37, P < 0.001 for chronic MSK pain 17 |
| DASS-D | Moderate | r = −0.59, P < 0.001 for chronic MSK pain 36 |
| DASS-D | Moderate | r = −0.51, P < 0.001 for PSEQ-2 on chronic MSK pain 36 |
| DASS-D | Low | Rho = −0.40, P < 0.01 for chronic MSK pain 45 |
| BDI | Low | r = −0.45, P < 0.001 for chronic MSK pain 31 |
| BDI | Low | r = −0.42, P < 0.001 for PSEQ-4 on chronic MSK pain 31 |
| BDI | Low | r = −0.32, P < 0.001 for PSEQ-2 on chronic MSK pain 31 |
| Catastrophizing | ||
| PCS | Moderate | r = −0.68, P < 0.001 for chronic MSK pain 1 |
| PCS | Moderate | Rho = −0.59, P < 0.05 for chronic neck pain 15 |
| PCS | Low | r = −0.49, P < 0.001 for chronic MSK pain 2 |
| PCS | Low | r = −0.48, P < 0.001 for chronic MSK pain 13 |
| PCS | Low | Rho = −0.43, P < 0.01 for chronic MSK pain 45 |
| PCS | Low | r = −0.42, P < 0.001 for chronic MSK pain 17 |
| PCS | Low | r = −0.41, P < 0.001 for chronic MSK pain 25 |
| PCS | Low | r = −0.39, P < 0.001 for chronic MSK pain 31 |
| PCS | Low | r = −0,38, P < 0.001 for PSEQ-2 on chronic MSK pain 31 |
| PCS | Low | r = −0.36, P < 0.001 for PSEQ-4 on chronic MSK pain 31 |
| PBQ | High | r = −0.74, P < 0.001 for chronic MSK pain 35 |
| PRSS-C | Moderate | r = −0.50, P < 0.001 for PSEQ-2 on chronic MSK pain 36 |
| PRSS-C | Moderate | r = −0.55, P < 0.001 for chronic MSK pain 36 |
AVD-IASP-S, adapted version of the disability subscale of the International Association for the Study of Pain scale; BPI, Brief Pain Inventory; BDI, Beck Depression Inventory; DASS-D, Depression Anxiety Stress Scale-Depression; DASS-A, Depression Anxiety Stress Scale-Anxiety; HADS-A, Hospital Anxiety and Depression Scale-Anxiety subscale; HADS-D, Hospital Anxiety and Depression Scale-Depression subscale; MPI, Multidimensional Pain Inventory; PCS, Pain Catastrophizing Scale; PRSS-C, Pain Response Self-Statements Catastrophizing Scale; RMDQ, Roland–Maurice Disability Questionnaire; VAS, visual analogue scale.
Internal consistency was evaluated in most studies using Cronbach alpha. All studies were given a very good score on the COSMIN quality assessment tool for internal consistency. Twenty studies (5295 participants) 1–3,8,10,13,14,17,21–23,25,31,35–38,45,48,50 calculated Cronbach alpha for the PSEQ-10, with values ranging from 0.79 to 0.95. Six studies (1354 participants) 1,8,10,31,36,50 calculated Cronbach alpha for the PSEQ-2, with values ranging from 0.76 to 0.91. Two studies (430 participants) 1,31 calculated Cronbach alpha for the PSEQ-4, with values ranging from 0.87 to 0.90. Table Table5 5 presents ranges of Cronbach alphas. A score of 0.95 or higher may indicate a level of redundancy within the items of the questionnaire which was observed in 3 studies. 10,45,50
Summary of findings for internal consistency and reliability.
| n studies | n participants | Population | Range | Weighted mean | |
|---|---|---|---|---|---|
| Internal consistency (Cronbach alpha)PSEQ-10 | 20 | 5295 | Chronic MSK pain, upper limb MSK pain, chronic LBP, subacute and chronic neck pain, and fibromyalgia | 0.79–0.95 | N/A |
| Internal consistency (Cronbach alpha)PSEQ-4 | 2 | 430 | Chronic MSK pain | 0.87–0.90 | N/A |
| Internal consistency (Cronbach alpha)PSEQ-2 | 6 | 1354 | Chronic MSK pain, upper limb MSK pain, and chronic LBP | 0.76–0.91 | N/A |
| Test–retest reliability (ICC) | |||||
| PSEQ-10 | 10 | 908 | Chronic MSK pain, upper limb MSK pain, chronic LBP, and fibromyalgia | 0.75–0.93 | 0.86 |
| PSEQ-2 | 3 | 422 | Chronic MSK pain, upper limb MSK pain, and chronic LBP | 0.79–0.88 | 0.85 |
| Absolute reliability (SEM) | |||||
| PSEQ-10 | 3 | 356 | Chronic MSK pain and chronic LBP | 1.23–5.66 | 3.37 |
| Absolute reliability (MDC95) | |||||
| PSEQ-10 | 3 | 273 | Chronic MSK pain, and chronic LBP | 3.41–15.69 | 11.52 |
ICC, intraclass correlation coefficient; MDC95, minimal detectable change at 95% confidence interval; MSK, musculoskeletal; LBP, low back pain.
Test–retest reliability was evaluated using ICC in 11 studies (1016 participants). 2,3,10,14,17,21,25,29,36,37,50 COSMIN risk of bias of reliability was rated as very good for 2 included studies, 3,37 adequate for 4 studies, 14,17,36,50 doubtful for 4 studies, 2,21,25,29 and inadequate for 1 study. 10 Table Table5 5 presents weighted means and ranges of ICCs. Intraclass correlation coefficients for the PSEQ-10 ranged from 0.75 to 0.93 with an overall weighted mean of 0.86 (10 studies; 908 participants), which represents an excellent reliability overall. Intraclass correlation coefficients for the PSEQ-2 ranged from 0.79 to 0.88 with an overall weighted mean of 0.85 (3 studies; 422 participants), which represents an excellent reliability. The reliability of the PSEQ-4 has not been evaluated yet.
Four studies (381 participants) 10,17,21,29 evaluated the absolute reliability of the PSEQ-10 by calculating SEM or MDC. COSMIN risk of bias of measurement error was rated as adequate for 1 included study, 17 doubtful for 2 studies, 21,29 and inadequate for 1 study. 10 SEM, which represents the standard deviation of the PSEQ-10 score, ranged from 1.23 to 5.66 (weighted mean of 3.37 [3 studies; 356 participants). 10,17,21 MDC95, which represents the estimate of the smallest amount of change that can be detected between 2 measurements representing a real difference between the same 2 measurements, ranged from 3.41 to 15.69 (weighted mean of 11.52 [3 studies; 273 participants]). 17,21,29
Responsiveness was evaluated in 4 studies 15,16,29,36 using ES, SRM, and MCID. COSMIN risk of bias for responsiveness was rated as very good for 3 included studies 15,16,29 and inadequate for 1 study. 36 Nicholas et al. 36 reported a large effect size (0.92) and SRM (0.94) for the PSEQ-2 in a population with chronic pain (140 participants) that had just participated in a cognitive intervention that aimed, in part, to modify self-efficacy. When analyzing results from those who improved (increase of 2 or more on the PSEQ-2 score), the ES and SRM increased to 1.54 and 2.22, respectively. In subjects who were classified as not improved (increase of less than 2 on the PSEQ-2 score), the ES and SRM decreased to 0.15 and 0.30, respectively. Chiarotto et al. 16 evaluated responsiveness in a sample (n = 104) of patients with chronic LBP, regardless of whether they improved or not, who had received a multimodal physical therapy intervention partially designed to modify self-efficacy. They reported an ES and SRM of 0.53 and 0.63 for the PSEQ-10, 0.46 and 0.50 for the PSEQ-2, and 0.46 and 0.54 for the PSEQ-4. These values represent a small to moderate change. Finally, Chiarotto et al. 15 reported ES and SRM values of 0.73 and 1.15 in a sample of patients (146 participants) with neck pain disorders after 10 sessions of multimodal physical therapy over 5 weeks. When analyzed in subgroups, responsiveness was higher in patients with idiopathic neck pain (ES: 1.36 and SRM: 1.21) compared with patients with whiplash-associated disorder (ES: 0.57 and SRM: 1.09). Finally, reported MCID values ranged from 5.5 to 8.5 points of 60 for the PSEQ-10 in a population of chronic LBP (2 studies; 151 participants; sensitivity (Sn) = 0.648; specificity (Sp) = 0.875; area under the curve (AUC) = 0.73 to 0.79), 16,29 whereas 1 study reported a MCID of 1.5 of 12 for the PSEQ-2 (1 study; 103 participants; Sn = 0.507; Sp = 0.844; AUC = 0.75) and 1.5 of 24 for the PSEQ-4 (1 study; 103 participants; Sn = 0.803; Sp = 0.687; AUC = 0.81) for chronic LBP. 16 To determine MCID, participants were dichotomized based on patients' self-reported improvement on the global perception of change scales, which were either general 16,29 or specific to self-efficacy. 16 Patients classifying themselves on the global perception of change scales as “totally improved,” “much improved,” and “rather improved” were considered improved; those who described themselves as “slightly improved,” “unchanged,” and “slightly worsened” were considered as unchanged.
Several studies assessed the psychometric properties of the translated and adapted versions of the PSEQ-10 or one of its shortened versions in languages such as Amharic, 14 Chinese-Hong Kong 25 , Chinese-Mainland, 50 Catalan, 13 Danish, 37 Italian, 17 Japanese, 2 Mongolian, 45 Persian, 3 Portuguese-Brazilian, 38 Portuguese-European, 22 and Yoruba. 21 They all applied rigorous methods to complete the translation and cross-cultural adaptation process. 6 Fatoye et al. 21 modified item 7 “I can cope with my pain without medication” by adding a word related to charms to the Yoruba version to better reflect their traditional medical culture. Chala et al. 14 also adapted 2 items (2 and 10) to the local culture and context for the Amharic version. Other examples of tasks were added to item 2 “I can do most of the household chores (tidying up, washing dishes, etc), despite the pain” to better reflect household chores accomplished by men (making a bed, picking things up, cooking a meal, splitting firewood, etc). Finally, the word “physically” was added to item 10 “I can gradually become more active, despite pain” because the Amharic translation of “active” is broad and can result in other interpretations of its meaning such as ones related to the level of consciousness. Mean and standard deviation scores of the PSEQ-10 obtained from those cross-cultural adaptations are presented in Table Table6 6 .
Mean and standard deviation scores of the PSEQ-10 obtained from cross-cultural adaptations.
| Version | Population | n | Mean score (SD) |
|---|---|---|---|
| Amharic 14 | Chronic low back pain | 240 | 43.8 (12.0) |
| Catalan 13 | Chronic MSK pain | 227 | 21.28 (5.94) |
| Chinese-Hong Kong 25 | Chronic MSK pain | 120 | 28.5 (13.3) |
| Chinese-Mainland 50 | Chronic MSK pain | 219 | 32.74 (13.18) |
| Danish 37 | Fibromyalgia | 99 | 27.32 (5.12) |
| English 35 | Chronic MSK pain | 1306 | 23.0 (12.7) |
| Italian 17 | Chronic low back pain | 165 | 36.12 (12.90) |
| Japanese 2 | Chronic MSK pain | 176 | 33.06 (13.51) |
| Mongolian 45 | Chronic MSK pain | 142 | 36.7 (15.3) |
| Nigerian 46 | Chronic MSK pain | 256 | Not available |
| Persian 3 | Chronic MSK pain | 517 | 36.7 (14.3) |
| Portuguese-Brazilian 38 | Chronic MSK pain | 311 | 34.8 (14.8) |
| Portuguese-European 22 | Chronic MSK pain | 174 | 40.83 (11.31) |
| Yoruba 21 | Chronic low back pain | 131 | Not available |
MSK, musculoskeletal; PSEQ, Pain Self-Efficacy Questionnaire.
Boxes of the COSMIN risk of bias tool
Development 1b. Cognitive interview study or other pilot test Content validity 2a. Asking patient about relevance 2b. Asking patient about comprehensiveness 2c. Asking patient about comprehensibility 2d. Asking professionals about relevance 2e. Asking professionals about relevance Structural validity Internal consistency Cross-cultural Validity Reliability Measurement error Criterion validity Construct validity 9a. Comparison with other outcome measurement instruments (convergent validity) 9b. Comparison between subgroups (discriminative or known-groups validity) Responsiveness 10a. Criterion approach (I.E. comparison to a gold standard)10b. Construct approach (ie, hypotheses testing: comparison with other outcome measurement instruments)
10c. Construct approach: (I.E. hypotheses testing: comparison between subgroups) 10d. Construct approach: (I.E. hypotheses testing: before and after intervention)V=very good, A = adequate, D = doubtful, I=inadequate, - = not applicable.
Two studies (299 participants) reported the time to complete the PSEQ-10. 17,23 Kortlever et al. 23 reported that participants took an average of 78 seconds (range: 24–316 seconds; IQR: 60–101 seconds) to complete the PSEQ-10 (original English version), whereas Chiarotto et al. 17 reported a median time of completion of 180 seconds (IQR: 120–300 seconds) for the PSEQ-10/Italian.
This study summarized evidence from 28 studies including 9853 participants with various MSK disorders who completed the PSEQ-10 or one of its shortened versions (PSEQ-2 and/or PSEQ-4). The PSEQ is a unidimensional measurement tool to assess pain-related self-efficacy in populations with chronic pain, including MSK disorders. It has been adapted and validated in 14 languages which make it easier to use in several countries. Hypotheses on construct validity were confirmed in most included studies showing that the PSEQ is positively correlated with quality of life measures and negatively correlated with measures of disability, pain, pain interference, anxiety, depression, and catastrophizing. These divergent and convergent construct validity results show that patients with higher pain self-efficacy have a better quality of life and lower levels of physical and mental symptoms.
Internal consistency is excellent overall for all versions of the PSEQ. A high Cronbach alpha score (≥0.95) indicates that certain items may be redundant. 42 Given that the PSEQ-10 Cronbach alpha was 0.95 for 3 included studies, it is possible that a certain level of redundancy is present within the questionnaire. However, because this high score was only found in 3 studies of 20 and that no study suggested redundancy nor the removal of an item based on factor loading analysis, the internal consistency was considered excellent. Another key point highlighted by authors was that item 7 of the questionnaire, “I can cope with my pain without medication,” constantly had the lowest factor loading and correlation with other items. 17,19,20,25,35,38 One possible explanation for this could be that this item does not strictly measure the construct of self-efficacy or is the item that measures it the least. 20 Another reason could be that patients can cope well with their pain but rely heavily on their medication to do so. Test–retest reliability and MDC95 also showed excellent overall values. Clinicians can consider MDC95 to be 11.5 of 60 PSEQ-10 points (representing 19% of the total score) in the population with chronic LBP. A MDC higher than the MCID means that the MDC needs to be considered as the relevant value to determine whether a change has truly occurred between 2 measurements in time and whether the change is clinically relevant. 24
Floor and ceiling effects were extracted and analysed. Floor effects refer to the capacity of a test to discriminate among patients with lower scores on the test. On the other hand, the ceiling effect refers to the capacity of a test to discriminate among patients with higher scores on the test. 43 If 15% or fewer participants achieve the lowest or highest available score, the effect is considered to be acceptable. 30 The PSEQ-10 and its short versions did not demonstrate a floor effect in any study, signifying that the measure is able to differentiate among people who have low pain self-efficacy. The PSEQ-10 ceiling effect was acceptable; however, the PSEQ-2 (version with items 8 and 9) ceiling effect was high, implying that the short form is less able to differentiate among patients with a higher level of pain self-efficacy. This suggests that the PSEQ-2 should not be used in place of the original version.
Clinicians can consider the MCID of the PSEQ-10 to range between 5.5 and 8.5 of 60 PSEQ-10 points (representing between 9% and 14% of the total score). MCIDs of the PSEQ-2 and PSEQ-4 were determined to be 1.5 of 12 points (12.5% of the total score) and 1.5 of 24 points (6.25% of the total score), respectively, in the population with chronic LBP. However, because few studies have evaluated it, the responsiveness needs to be further investigated, especially in populations other than chronic LBP. A few included studies reported the responsiveness of the PSEQ-10 by describing ES and SRM values. 15,16,36 Because it is complex to assess changes in a construct such as self-efficacy, it is difficult to calculate responsiveness values in people who improved their pain self-efficacy. Only 1 study 16 used the global perception of change scale specific to the construct of self-efficacy. All other studies 15,29,36 reporting on responsiveness used the global perception of change scale rated on the impression of general improvement in patients with chronic low back or neck pain which can lead to a bias for the change calculation of pain self-efficacy–specific construct. Observed ES and SRM values demonstrated that the PSEQ-10, PSEQ-4, and PSEQ-2 are responsive enough to be used in a clinical or research context to evaluate changes after an intervention on chronic MSK disorders, chronic LBP, and chronic neck pain, including whiplash-associated disorders.
To the best of our knowledge, this is the first systematic review, with a complete reported methodological quality appraisal process, assessing PSEQ psychometric properties in the population with chronic MSK pain. However, other reviews have reported PSEQ properties, and their results lean in the same direction.
Miles et al. 32 published a systematic review in 2011 where they looked at different patient-reported outcome measures for self-efficacy in a population with chronic pain. However, they did not mention the use of a methodological quality appraisal tool. Among all studies included, 14 of them reported values for the PSEQ. Authors of the systematic review concluded that the PSEQ had good content and construct validity (correlations with measures of anxiety, depression, pain ratings, and unhelpful coping strategies) which is similar to the current findings. They also mentioned that the PSEQ was easy to score and quick to administer (
In 2018, Banerjee et al. 5 published a systematic review of the psychometric properties of self-management questionnaires used in clinical trials with patients with chronic pain. They reported risk of bias of the methodology of those trials, but not for the assessment of each psychometric property. Surprisingly, they included only 7 studies using the PSEQ compared with 28 in the current review. Based on those 7 studies, the authors concluded that the PSEQ had good content and construct validity as well as good internal consistency which are results that align with our findings.
Finally, a 2020 systematic review by Vergeld et al., 47 which included 47 studies (14 of them reporting on the PSEQ-10), assessed psychometric properties of the PSEQ-10 when used with a population with LBP. They reported excellent internal consistency, with Cronbach alpha ranging from 0.88 to 0.94 and excellent test–retest reliability with ICCs ranging from 0.82 to 0.92. These values are similar to the findings of the present review. However, they did not provide information on study quality assessment and data extraction. Similarly to Miles et al., 32 they also suggested that future studies look at PSEQ responsiveness because there were not enough data to conclude on this property.
The results from this study show that the PSEQ is suitable to be used in clinical practice to measure patients' level of pain self-efficacy and its evolution in time. The MDC of 11.5 of the PSEQ-10 can be used as the MCID to assess change over a period ranging from 4 to 12 weeks. The PSEQ-10 is relatively short to complete, and it has been translated in different languages making it a useful tool in both clinical and research settings in several countries. Clinician can use the PSEQ-2 for a screening purpose as suggested by Bot et al. and Nicholas et al. 8,36 However, given that there are 2 versions of the PSEQ-2 which can be confusing, that the full version PSEQ-10 is short to complete, that the ceiling effect of the PSEQ-2 is high, and that the PSEQ-4 has not been studied enough, it is our opinion that short forms are less valuable in clinic and research settings.
Although this systematic review was conducted using a rigorous method and a previously validated and comprehensive study quality assessment tool, some limitations can be identified. First, because we limited our literature search to 3 databases, we may have missed some potential articles. We are, however, quite confident that the databases used allowed us to perform an extensive search of the literature, especially because reference lists of all retrieved studies and previous reviews were searched for further relevant studies. Second, we only searched for articles written in French or English, which could have limited the scope of our results and prevented us from including relevant articles written in other languages. However, no study was excluded in the selection phase based on language.
This study also had several strengths because it constitutes an extensive and up-to-date review of the literature regarding the psychometric properties of the PSEQ when used in populations with MSK disorders. It was conducted using validated guidelines and represents an improvement in methodological quality compared with previous reviews where methodology for data extraction was not described and authors did not perform a quality assessment of included studies to evaluate their risk of bias.
Based on our results, future research evaluating this questionnaire's psychometric properties could improve reliability testing methods because this category had the lowest COSMIN score. Such studies should make sure to document the similarity between the 2 measurement conditions and the time interval between administrations. In addition, they should document whether patients were stable or not during the interval period in-between measurements, using tools such as the Global Rating of Change scales. Finally, further studies are needed to establish MDC and MCID values for populations other than chronic LBP because there are currently values available for this population alone.
The PSEQ is a robust and frequently used questionnaire assessing pain self-efficacy in chronic MSK disorders. Methods used for most of the measurement properties evaluated were of adequate to very good quality (76/92; 90%) according to the COSMIN risk of bias tool. The PSEQ has good content validity and structural validity which shows that every version of the PSEQ is a unidimensional questionnaire. Construct validity shows low to moderate correlations with measures of quality of life, disability, pain, pain interference, anxiety, depression, and catastrophizing. Concurrently, a high correlation between the PSEQ-10 and the 2 versions of the PSEQ-2 was found. Test–retest reliability and internal consistency are excellent. Pooled estimates of SEM (3.37) and MDC (11.52) were calculated and deemed good. MCID ranged from 5.5 to 8.5 of 60 in patients with chronic LBP which are lower than the MDC meaning that the MDC can be used to measure change by clinicians and researchers. The results of this study suggest that clinicians can use the questionnaire with confidence to measure the pain self-efficacy state of patients and their change in time. Further high-quality studies are needed to determine MCID in populations other than chronic LBP.
The authors have no conflicts of interest to declare.
The authors want to acknowledge Charles Batcho for his guidance and advice throughout the production process. They also acknowledge Marianne Roos for her contribution to the English language review of the manuscript. M-O. Dubé and P. Langevin are supported by Training Scholarships from the Fonds de Recherche Québec-Santé (FRQ-S). J.-S. Roy is supported by salary awards from the FRQ-S. Review was not registered, and there is no available protocol for the present review. The data that support the findings of this study are available from the corresponding author, JSR, on reasonable request.
Authors Contribution: M.-O. Dubé and P. Langevin conceived and designed the review. They conducted the literature search, extracted the data, and wrote the manuscript. J.-S. Roy commented on the draft of the manuscript. All authors have seen and approved the final version.
Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.
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