Method of administration of PROMIS scales did not significantly impact score level, reliability, or validity
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AuthorsBjorner, Jakob B.
Rose, Matthias S. F.
Gandek, Barbara L.
Stone, Arthur A.
Junghaenel, Doerte U.
Ware, John E. Jr.
UMass Chan AffiliationsDepartment of Quantitative Health Sciences
Document TypeJournal Article
Aged, 80 and over
*Outcome Assessment (Health Care)
Reproducibility of Results
Health Services Research
MetadataShow full item record
AbstractOBJECTIVES: To test the impact of the method of administration (MOA) on score level, reliability, and validity of scales developed in the Patient Reported Outcomes Measurement Information System (PROMIS). STUDY DESIGN AND SETTING: Two nonoverlapping parallel forms each containing eight items from each of three PROMIS item banks (Physical Function, Fatigue, and Depression) were completed by 923 adults with chronic obstructive pulmonary disease, depression, or rheumatoid arthritis. In a randomized crossover design, subjects answered one form by interactive voice response (IVR) technology, paper questionnaire (PQ), personal digital assistant (PDA), or personal computer (PC) and a second form by PC, in the same administration. Method equivalence was evaluated through analyses of difference scores, intraclass correlations (ICCs), and convergent/discriminant validity. RESULTS: In difference score analyses, no significant mode differences were found and all confidence intervals were within the prespecified minimal important difference of 0.2 standard deviation. Parallel-forms reliabilities were very high (ICC = 0.85-0.93). Only one across-mode ICC was significantly lower than the same-mode ICC. Tests of validity showed no differential effect by MOA. Participants preferred screen interface over PQ and IVR. CONCLUSION: We found no statistically or clinically significant differences in score levels or psychometric properties of IVR, PQ, or PDA administration compared with PC.
SourceJ Clin Epidemiol. 2014 Jan;67(1):108-13. doi: 10.1016/j.jclinepi.2013.07.016. Link to article on publisher's site
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/30463
Co-author Barbara Gandek is a doctoral student in the Clinical and Population Health Research Program in the Graduate School of Biomedical Sciences (GSBS) at UMass Medical School.
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