Designing a Clinical Trial to Prevent Medical Errors Essay

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Errors associated with patient treatment are widespread, resulting in negative outcomes. Mistake prevention in clinical treatment is generally understood, and a vast body of research studying preventative measures exists. On the other hand, direct care errors are not the only things that can hurt patients. Clinical research errors can significantly affect medical outcomes by altering the quality of care for hundreds of clients if they are substantial enough to influence the researchers’ conclusions. Several studies have found that inaccuracies in clinical investigation records are prevalent. Despite this, less is understood about the different types of errors found in scientific databases, their features, and their potential impact on study conclusions.

Ensuring correct and available information will minimize the common sources of error in clinical research databases. Implementing integrity checks, which identify data entries that are impossible or internally inconsistent, is a basic approach to identifying errors. However, they only assess the information for a restricted number of scenarios; hence the error rate is likely to be underestimated (Goldberg et al., 2008). More comprehensive cognitive integration of datasets would almost certainly reduce error rates by applying dynamic limitations that change depending on the situation of other variables in the database. Double-entry or other methods, including read-aloud data entry, could be used in high-value data entry; however, the cost of implementation could be high.

Failure to delegate responsibilities and insufficiency of master data management are two possible hurdles to good data reliability in clinical research databases. The data analysis throughout the data input procedure will improve with the appropriate training of the research staff. In addition, when compared to paper-based forms, electronic data collecting forms result in lower mistake counts, such as missing and illegible values, improving data quality. Therefore, electronic data capturing produces higher-quality data and is an important approach for improving poor data integrity.

In conclusion, data structuring and entry and the influence of data integrity on clinical results are frequently unknown to research study teams. Clinical research studies require high-quality data, using electronic data capture technologies, staff skills training, adherence to data handling best standards, and prior engagement with data analysts to boost the research. These are some vigilant efforts to minimize errors in clinical research databases, thereby creating a robust research operation.

Reference

Goldberg, S. I., Niemierko, A., and Turchin, A. (2008). . AMIA Symposium Proceedings, 242-246. Web.

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IvyPanda. (2024, March 3). Designing a Clinical Trial to Prevent Medical Errors. https://ivypanda.com/essays/designing-a-clinical-trial-to-prevent-medical-errors/

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"Designing a Clinical Trial to Prevent Medical Errors." IvyPanda, 3 Mar. 2024, ivypanda.com/essays/designing-a-clinical-trial-to-prevent-medical-errors/.

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IvyPanda. (2024) 'Designing a Clinical Trial to Prevent Medical Errors'. 3 March.

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IvyPanda. 2024. "Designing a Clinical Trial to Prevent Medical Errors." March 3, 2024. https://ivypanda.com/essays/designing-a-clinical-trial-to-prevent-medical-errors/.

1. IvyPanda. "Designing a Clinical Trial to Prevent Medical Errors." March 3, 2024. https://ivypanda.com/essays/designing-a-clinical-trial-to-prevent-medical-errors/.


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IvyPanda. "Designing a Clinical Trial to Prevent Medical Errors." March 3, 2024. https://ivypanda.com/essays/designing-a-clinical-trial-to-prevent-medical-errors/.

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