Recommendations to address respondent burden associated with patient-reported outcome assessment
Author:
Funder
Merck KGaA
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41591-024-02827-9.pdf
Reference61 articles.
1. Aiyegbusi, O. L. et al. Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection. Nat. Commun. 13, 6026 (2022).
2. Aiyegbusi, O. L., Nair, D., Peipert, J. D., Schick-Makaroff, K. & Mucsi, I. A narrative review of current evidence supporting the implementation of electronic patient-reported outcome measures in the management of chronic diseases. Ther. Adv. Chronic Dis. 12, 20406223211015958 (2021).
3. Cruz Rivera, S. et al. The impact of patient-reported outcome (PRO) data from clinical trials: a systematic review and critical analysis. Health Qual. Life Outcomes 17, 156 (2019).
4. Cruz Rivera, S. et al. Patient-reported outcomes in the regulatory approval of medical devices. Nat. Med. 27, 2067–2068 (2021).
5. Calvert, M., Kyte, D., Price, G., Valderas, J. M. & Hjollund, N. H. Maximising the impact of patient-reported outcome assessment for patients and society. BMJ 364, k5267 (2019).
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