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Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection

Aiyegbusi, Olalekan Lee
; 
Roydhouse, Jessica
; 
Rivera, Samantha Cruz
; 
Kamudoni, Paul
; 
Schache, Peter
; 
Wilson, Roger
; 
Stephens, Richard
; 
Calvert, Melanie
Abstract
Patient-reported outcomes (PROs) are used in clinical trials to provide evidence of the benefits and risks of interventions from a patient perspective and to inform regulatory decisions and health policy. The collection of PROs in routine practice can facilitate monitoring of patient symptoms; identification of unmet needs; prioritisation and/or tailoring of treatment to the needs of individual patients and inform value-based healthcare initiatives. However, respondent burden needs to be carefully considered and addressed to avoid high rates of missing data and poor reporting of PRO results, which may lead to poor quality data for regulatory decision making and/or clinical care.
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Date
2022-10-12
Type
Article
Subject
Patients. Primary care. Medical profession. Forensic medicine
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UHB Health Care Services
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Citation
Aiyegbusi OL, Roydhouse J, Rivera SC, Kamudoni P, Schache P, Wilson R, Stephens R, Calvert M. Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection. Nat Commun. 2022 Oct 12;13(1):6026. doi: 10.1038/s41467-022-33826-4
Journal / Source Title
Nature Communications
DOI
10.1038/s41467-022-33826-4
URI
http://hdl.handle.net/20.500.14200/2364
PMID
36224187
Publisher
Nature Publishing Group
Publisher’s URL
http://www.nature.com/ncomms/index.html
https://www.ncbi.nlm.nih.gov/pmc/?term=%22Nat+Commun%22%5Bjournal%5D
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