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Original Article

Reliability, validity and ability to detect change of the clinician-rated Personal and Social Performance scale in patients with acute symptoms of schizophrenia

, , , , , & show all
Pages 325-338 | Accepted 10 Nov 2008, Published online: 07 Jan 2009
 

ABSTRACT

Objective: To describe the measurement properties of the Personal and Social Performance scale (PSP), a clinician-reported measure of severity of personal and social dysfunction, in subjects with acute symptoms of schizophrenia.

Methods: Pooled data from three paliperidone extended-release clinical studies (n = 1665) and data from a separate noninterventional, cross-sectional, validation study (n = 299) were analyzed.

Results: The PSP showed good interrater (intraclass correlation coefficient [ICC] = 0.87) and test–retest (ICCs > 0.90) reliability. Pearson correlation coefficient for association between baseline PSP and Positive and Negative Syndrome Scale (PANSS) total scores was −0.32 for subjects assessed by the same rater and −0.29 for subjects assessed by different raters, suggesting low overlap in measurement constructs between the PANSS and PSP. Spearman Rank correlation coefficient for association between baseline PSP and Clinical Global Impression-Severity (CGI-S) scores was −0.51 with the same rater and −0.15 with different raters. Hypothesized relationships between the PSP and the PANSS or CGI-S based on levels of disease severity were prospectively defined. These hypotheses were confirmed by analyses showing statistically significant differences between baseline mean PSP scores in subjects grouped by severity rating on the CGI-S (mild or less vs. at least moderate) (p < 0.001) and the PANSS (‘low symptom severity’ vs. ‘high symptom severity’) (p = 0.005). The PSP was sensitive to change based on statistically significant correlations between change in the PSP and change in the CGI-S (p < 0.001) and the PANSS (p < 0.001). Limitations of analyses include pooling data across studies, interrater reliability assessment in the validation study only, post hoc assessment of test–retest reliability in the paliperidone ER studies, different raters for the PSP and PANSS not specified in the paliperidone ER studies, PSP validity assessment based on the PANSS and the CGI-S as comparators rather than another social function instrument.

Conclusion: These initial reliability and validity assessments suggest the PSP has promise as a measure of social functioning in patients with acute symptoms of schizophrenia.

Acknowledgments

Declaration of interest: This report was supported by Johnson & Johnson Pharmaceutical Research and Development and Johnson & Johnson Pharmaceutical Services, LLC. D. P. has received consultation fees from Johnson & Johnson for work on schizophrenia. T. B. has received payment for lectures, consultancies, and unrestricted educational grants from Eli Lilly, Janssen Pharmaceutica, and Bristol Myers Squibb. M. R., D. G. and I. A. are employees of Johnson & Johnson and own stock and stock options in Johnson & Johnson. D. W. is an employee of Oxford Outcomes Ltd, which was contracted by Johnson & Johnson to conduct the outcomes validation study in subjects with acute symptoms of schizophrenia. P. M. passed away during the journal's peer review of this manuscript but had no conflict of interest. Katrien Peeters was instrumental in the design and conduct of the validation study. Karen M. Miner assisted in the preparation of the manuscript.

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