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
Aiyegbusi, Olalekan Lee
Roydhouse, Jessica
Rivera, Samantha Cruz
Kamudoni, Paul
Schache, Peter
Wilson, Roger
Stephens, Richard
Calvert, Melanie
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2022-10-12
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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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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
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