Browsing Institute of Population Health Sciences by Subject "Data Collection"
Now showing items 1-3 of 3
-
Barriers and enablers to routine register data collection for newborns and mothers: EN-BIRTH multi-country validation study.
(BioMed Central, 2021-03-26)BACKGROUND: Policymakers need regular high-quality coverage data on care around the time of birth to accelerate progress for ending preventable maternal and newborn deaths and stillbirths. With increasing facility births, ... -
Study within a trial of electronic versus paper-based Patient-Reported oUtcomes CollEction (SPRUCE): study protocol for a partially randomised patient preference study.
(2023-09-21)INTRODUCTION: Patient-reported outcomes (PRO) are currently collected from trial participants using paper questionnaires by the Clinical Trials and Statistics Unit at The Institute of Cancer Research (ICR-CTSU). Streamlining ... -
Using systematic data categorisation to quantify the types of data collected in clinical trials: the DataCat project.
(2020-06-16)BACKGROUND: Data collection consumes a large proportion of clinical trial resources. Each data item requires time and effort for collection, processing and quality control procedures. In general, more data equals a heavier ...