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Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection
Citation
Aiyegbusi, OL and Roydhouse, J and Cruz Rivera, S and Kamudoni, P and Schache, P and Wilson, R and Stephens, R and Calvert, M, Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection, Nature Communications, 13, (1) Article 6026. ISSN 2041-1723 (2022) [Refereed Article]
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Copyright Statement
© 2022. The Authors. This article is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) License (https://creativecommons.org/licenses/by/4.0/), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
DOI: doi:10.1038/s41467-022-33826-4
Abstract
Item Details
Item Type: | Refereed Article |
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Keywords: | patient-reported outcomes, respondent burden, data collection |
Research Division: | Health Sciences |
Research Group: | Health services and systems |
Research Field: | Health services and systems not elsewhere classified |
Objective Division: | Health |
Objective Group: | Evaluation of health and support services |
Objective Field: | Evaluation of health outcomes |
UTAS Author: | Roydhouse, J (Dr Jessica Roydhouse) |
ID Code: | 153890 |
Year Published: | 2022 |
Deposited By: | Menzies Institute for Medical Research |
Deposited On: | 2022-10-13 |
Last Modified: | 2022-11-28 |
Downloads: | 0 |
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