Responsiveness of the Acne-Specific Quality of Life Questionnaire (Acne-QoL) to treatment for acne vulgaris in placebo-controlled clinical trials
dc.contributor.author | McLeod, L. D. | en_US |
dc.contributor.author | Arbit, D. I. | en_US |
dc.contributor.author | Martin, A. R. | en_US |
dc.contributor.author | Fehnel, S. E. | en_US |
dc.contributor.author | Brandman, J. | en_US |
dc.contributor.author | McLaughlin-Miley, C. J. | en_US |
dc.contributor.author | Coombs, J. H. | en_US |
dc.contributor.author | Girman, Cynthia J. | en_US |
dc.date.accessioned | 2006-09-08T21:34:31Z | |
dc.date.available | 2006-09-08T21:34:31Z | |
dc.date.issued | 2002-12 | en_US |
dc.identifier.citation | Fehnel, S.E.; McLeod, L.D.; Brandman, J.; Arbit, D.I.; McLaughlin-Miley, C.J.; Coombs, J.H.; Martin, A.R.; Girman, C.J.; (2002). "Responsiveness of the Acne-Specific Quality of Life Questionnaire (Acne-QoL) to treatment for acne vulgaris in placebo-controlled clinical trials." Quality of Life Research 11(8): 809-816. <http://hdl.handle.net/2027.42/43563> | en_US |
dc.identifier.issn | 0962-9343 | en_US |
dc.identifier.issn | 1573-2649 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/43563 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12482164&dopt=citation | en_US |
dc.description.abstract | The Acne-Specific Quality of Life Questionnaire (Acne-QoL) was developed to measure the impact of facial acne across four dimensions of patient quality of life. The main objective of the current study was to evaluate the responsiveness of this instrument. Secondarily, this study provided an opportunity to extend the developer's psychometric validation. The Acne-QoL was utilized in two randomized, double-blind, placebo-controlled studies of the efficacy of Estrostep ® (norethindrone acetate/ethinyl estradiol) in the treatment of facial acne; a total of 296 Estrostep ® and 295 placebo patients were evaluated. The Acne-QoL was completed at the beginning, middle (cycle 3), and end (cycle 6) of the 6-month treatment period. The responsiveness of the Acne-QoL was demonstrated through its ability to detect both small (baseline to mid-study) and moderate (baseline to study end) treatment advantages for Estrostep ® patients. Confirmatory factor analysis supported the subscale structure, and internal consistency estimates were excellent. Convergent and discriminant validity were supported by correlations between Acne-QoL scores and clinical measures that were both in the direction and relative magnitude hypothesized. Finally, item response theory analyses confirmed that each item is highly related to its subscale's latent construct and that each subscale is sensitive across a broad range of the underlying continuum. The results of this evaluation confirm that the Acne-QoL is responsive, internally consistent, and valid. | en_US |
dc.format.extent | 292308 bytes | |
dc.format.extent | 3115 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Kluwer Academic Publishers; Springer Science+Business Media | en_US |
dc.subject.other | Skin Diseases | en_US |
dc.subject.other | Medicine & Public Health | en_US |
dc.subject.other | Public Health/Gesundheitswesen | en_US |
dc.subject.other | Quality of Life Research | en_US |
dc.subject.other | Sociology | en_US |
dc.subject.other | Acne Vulgaris | en_US |
dc.subject.other | Facial Dermatoses | en_US |
dc.subject.other | Psychometrics | en_US |
dc.subject.other | Quality of Life | en_US |
dc.title | Responsiveness of the Acne-Specific Quality of Life Questionnaire (Acne-QoL) to treatment for acne vulgaris in placebo-controlled clinical trials | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | University of Michigan/Pfizer Pharmacoeconomics and Outcomes Research Fellowship, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationother | Department of Epidemiology, Merck Research Laboratories, West Point, PA, USA | en_US |
dc.contributor.affiliationother | RTI Health Solutions, Research Triangle Institute, Research Triangle Park, NC, USA | en_US |
dc.contributor.affiliationother | RTI Health Solutions, Research Triangle Institute, Research Triangle Park, NC, USA | en_US |
dc.contributor.affiliationother | Pfizer Pharmaceutical Group, New York, NY, USA | en_US |
dc.contributor.affiliationother | Pfizer Pharmaceutical Group, New York, NY, USA | en_US |
dc.contributor.affiliationother | Pfizer Pharmaceutical Group, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationother | Department of Epidemiology, Merck Research Laboratories, West Point, PA, USA | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.identifier.pmid | 12482164 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/43563/1/11136_2004_Article_5089801.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1023/A:1020880005846 | en_US |
dc.identifier.source | Quality of Life Research | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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