Standardized study performance, quality assurance, and quality control in a cluster-randomized trial: the Pneumococcal Vaccine Schedules trial

Randomized controlled trials are considered the "gold standard" for evaluating the effectiveness of an intervention. However, large-scale, cluster-randomized trials are complex and costly to implement. The generation of accurate, reliable, and high-quality data is essential to ensure the validity and generalizability of findings. Robust quality assurance and quality control procedures are important to optimize and validate the quality, accuracy, and reliability of trial data. To date, few studies have reported on study procedures to assess and optimize data integrity during the implementation of large cluster-randomized trials. The dearth of literature on these methods of trial implementation may contribute to questions about the quality of data collected in clinical trials. Trial protocols should consider the inclusion of quality assurance indicators and targets for implementation. Publishing quality assurance and control measures implemented in clinical trials should increase public trust in the findings from such studies. In this manuscript, we describe the development and implementation of internal and external quality assurance and control procedures and metrics in the Pneumococcal Vaccine Schedules trial currently ongoing in rural Gambia. This manuscript focuses on procedures and metrics to optimize trial implementation and validate clinical, laboratory, and field data. We used a mixture of procedure repetition, supervisory visits, checklists, data cleaning and verification methods and used the metrics to drive process improvement in all domains.

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Publication Details

Journal
Trials
Published
2024-12-18
DOI
https://doi.org/10.1186/s13063-024-08677-7
Primary Topic
Ethics in Clinical Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Standardized study performance, quality assurance, and quality control in a cluster-randomized trial: the Pneumococcal Vaccine Schedules trial

Bubacarr Baldeh, Yekini Olatunji, Golam Sarwar, Momodou M. Drammeh et al.
Trials
Ethics in Clinical Research
article

Standardized study performance, quality assurance, and quality control in a cluster-randomized trial: the Pneumococcal Vaccine Schedules trial

Bubacarr Baldeh, Yekini Olatunji, Golam Sarwar, Momodou M. Drammeh, Banjo Adeshola, Williams Oluwatosin Adefila, Baleng Mahama Wutor, Abdoullah Nyassi, Grant Mackenzie, Ilias Hossain, Yasir Shitu Isa, Rasheed Salaudeen, Keita Modou Lamin, Minteh Molfa, Babila G Lobga, Yusuf Abdulsalam Olawale, Benjamin Young, Isaac Osei, Ebrimah Nyimanta, Barjo Ousman, Emmanuel Mendy
article en

Abstract

Randomized controlled trials are considered the "gold standard" for evaluating the effectiveness of an intervention. However, large-scale, cluster-randomized trials are complex and costly to implement. The generation of accurate, reliable, and high-quality data is essential to ensure the validity and generalizability of findings. Robust quality assurance and quality control procedures are important to optimize and validate the quality, accuracy, and reliability of trial data. To date, few studies have reported on study procedures to assess and optimize data integrity during the implementation of large cluster-randomized trials. The dearth of literature on these methods of trial implementation may contribute to questions about the quality of data collected in clinical trials. Trial protocols should consider the inclusion of quality assurance indicators and targets for implementation. Publishing quality assurance and control measures implemented in clinical trials should increase public trust in the findings from such studies. In this manuscript, we describe the development and implementation of internal and external quality assurance and control procedures and metrics in the Pneumococcal Vaccine Schedules trial currently ongoing in rural Gambia. This manuscript focuses on procedures and metrics to optimize trial implementation and validate clinical, laboratory, and field data. We used a mixture of procedure repetition, supervisory visits, checklists, data cleaning and verification methods and used the metrics to drive process improvement in all domains.

TrialsVol. 25(1)
The University of Melbourne (AU), London School of Hygiene & Tropical Medicine (GB), MRC Unit the Gambia (GM), Murdoch Children's Research Institute (AU), Ministry of Health and Social Welfare (GM)
Bill and Melinda Gates Foundation, London School of Hygiene and Tropical Medicine, Medical Research Charities Group, National Institute for Health and Care Research, Medical Research Council
Partnerships for the goals
Openalex Percentile: Top 64%
Ethics in Clinical Research
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