Difference in method of administration did not significantly impact item response: an IRT-based analysis from the Patient-Reported Outcomes Measurement Information System (PROMIS) initiative

Research output: Contribution to journalJournal articleResearchpeer-review

Jakob B Bjorner, Matthias Rose, Barbara Gandek, Arthur A Stone, Doerte U Junghaenel, John E Ware

PURPOSE: To test the impact of method of administration (MOA) on the measurement characteristics of items developed in the Patient-Reported Outcomes Measurement Information System (PROMIS).

METHODS: Two non-overlapping parallel 8-item forms from each of three PROMIS domains (physical function, fatigue, and depression) were completed by 923 adults (age 18-89) with chronic obstructive pulmonary disease, depression, or rheumatoid arthritis. In a randomized cross-over design, subjects answered one form by interactive voice response (IVR) technology, paper questionnaire (PQ), personal digital assistant (PDA), or personal computer (PC) on the Internet, and a second form by PC, in the same administration. Structural invariance, equivalence of item responses, and measurement precision were evaluated using confirmatory factor analysis and item response theory methods.

RESULTS: Multigroup confirmatory factor analysis supported equivalence of factor structure across MOA. Analyses by item response theory found no differences in item location parameters and strongly supported the equivalence of scores across MOA.

CONCLUSIONS: We found no statistically or clinically significant differences in score levels in IVR, PQ, or PDA administration as compared to PC. Availability of large item response theory-calibrated PROMIS item banks allowed for innovations in study design and analysis.

Original languageEnglish
JournalQuality of Life Research
Volume23
Issue number1
Pages (from-to)217-27
Number of pages11
ISSN0962-9343
DOIs
Publication statusPublished - Feb 2014

    Research areas

  • Adolescent, Adult, Aged, Aged, 80 and over, Arthritis, Rheumatoid, Cross-Over Studies, Data Collection, Depressive Disorder, Discrimination (Psychology), Female, Humans, Information Systems, Male, Middle Aged, Outcome Assessment (Health Care), Pulmonary Disease, Chronic Obstructive, Quality of Life, Questionnaires, Self Report, Sickness Impact Profile, Young Adult

ID: 138213345