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The level of subject participation and ED staff support in this pilot study argues for feasibility of data collection, intervention, and follow-up with this population.
We evaluate the feasibility of conducting a randomized controlled trial (RCT) of the CBCS-HCV with 12 study participants in Wave 1 testing to examine: (a) feasibility of intervention delivery; (b) patient acceptability; (c) recruitment, enrollment, retention; (d) feasibility of conducting a RCT; (d) therapist protocol fidelity; and (e) feasibility of data collection.
Within each domain are measures to evaluate factors like quality, validity and accuracy as well as the cost and feasibility of data collection.
Pre-testing also established the feasibility of data collection by research assistants with only 2 hours of training.
At the end of the study researchers were asked to give qualitative feedback on the conduct and feasibility of data collection.
The feasibility of data collection and the clinical and social significance of the indicators were initially tested with a sample of 236 children and adolescents from 27 institutions distributed in 7 regions.
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Respondents were asked to rate each QI adopting the RAND Appropriateness Methodology (scales 1 9, 1=extremely inappropriate; 9=extremely appropriate), according to the selection criteria of relevance, scientific soundness (validity, reliability, comparability) and feasibility (precise definition and specification, data feasibility, reliability of data collection).
Finally the process indicators were ranked by ordering them (highest to lowest) using scores achieved on attributes using the following sequence: feasibility with current data, feasibility with improvement of data collection methods and priority for reporting.
The primary foci of this study include assessment of: 1) the effect size of the intervention to power a larger study, 2) feasibility, 3) practicality of data collection procedures, 4) measurement adequacy, and 5) the ability to implement.
The feasibility and acceptability of data collection processes will be investigated through the number of missing items and follow-up rates relating to the clinical outcome measurements likely to be used in a phase III trial.
The feasibility of measuring indicators in terms of data collection and calculation.
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CEO of Professional Science Editing for Scientists @ prosciediting.com