Key considerations to reduce or address respondent burden in patient-reported outcome (PRO) data collection.
Nat Commun
; 13(1): 6026, 2022 10 12.
Article
em En
| MEDLINE
| ID: mdl-36224187
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.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Medidas de Resultados Relatados pelo Paciente
/
Política de Saúde
Idioma:
En
Ano de publicação:
2022
Tipo de documento:
Article