Healthy Skepticism Library item: 12282
Warning: This library includes all items relevant to health product marketing that we are aware of regardless of quality. Often we do not agree with all or part of the contents.
 
Publication type: Journal Article
Snyder CF, Watson ME, Jackson JD, Cella D, Halyard MY; Mayo/FDA Patient-Reported Outcomes Consensus Meeting Group.
Patient-reported outcome instrument selection: designing a measurement strategy.
Value Health 2007 Nov-Dec; 10:
http://www.ncbi.nlm.nih.gov/pubmed/17995477?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum
Abstract:
OBJECTIVE: To discuss issues in the design of a measurement strategy related to the use of patient-reported outcomes (PROs) in support of a labelling claim. METHODS: In association with the release by the US Food and Drug Administration of its draft guidance on the use of PROs to support labeling claims, the Mayo/FDA Patient-Reported Outcomes Consensus Writing Group was formed. This paper, part of a series of manuscripts produced by the Writing Group, focuses on designing a PRO measurement strategy. RESULTS: Developing a PRO measurement strategy begins with a clear statement about the proposed label claim that will derive from the PRO data. Investigators should identify the relevant domains to measure, develop a conceptual framework, identify alternative approaches for measuring the domains, and synthesize the information to design the measurement strategy. Often, there is not an already existing single instrument that has been developed and validated for the purposes of a given study. In such cases, investigators may consider supplementing an already existing questionnaire with additional scales or questions, modifying already existing instruments for a new application or patient population, or developing a new instrument altogether. The level of revalidation required for modifications and adaptations depends on the extent of the changes made. Revalidation requirements may range from cognitive testing/debriefing to confirm that subjects respond to the new instrument as expected to full-scale reliability and validity evaluations. CONCLUSION: A position of “reasonable pragmatism” is recommended such that the best available measurement strategy be considered as evidence for labeling.
Keywords:
Clinical Trials as Topic/statistics & numerical data*
Data Collection/methods*
Data Collection/statistics & numerical data
Humans
Patient Satisfaction/statistics & numerical data*
Product Labeling/standards*
Product Labeling/statistics & numerical data
Psychometrics
Research Design
Treatment Outcome*
United States
Validation Studies as Topic