Adapting international clinical trials during COVID-19 and beyond

Author:

Thriemer Kamala1ORCID,Degaga Tamiru Shibiru2,Alam Mohammad Shafiul3ORCID,Adhikari Bipin45,Tripura Rupam45,Hossain Mohammad Sharif3ORCID,Christian Michael6,Ghanchi Najia K7,Mnjala Hellen1,Weston Sophie1,Ley Benedikt1,Rumaseb Angela1,Tadesse Dagimawie2ORCID,Teferi Tedla8,Yilma Daniel9,Lee Grant1ORCID,Unger Holger1,Sutanto Inge10,Pasaribu Ayodhia Pitaloka11,Ghimire Prakash12ORCID,Beg Mohammad Asim7,Price Ric N145

Affiliation:

1. Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, NT, Australia

2. College of Medicine & Health Sciences, Arba Minch University, Arba Minch, Ethiopia

3. International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR, B), Dhaka, Bangladesh

4. Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand

5. Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK

6. Eijkman-Oxford Clinical Research Unit, Jakarta, Indonesia

7. Department of Pathology and Microbiology, Aga Khan University, Karachi, Pakistan

8. Arba Minch General Hospital, Arba Minch, Ethiopia

9. Jimma University, Jimma, Ethiopia

10. Department of Parasitology, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia

11. Department of Child Health, Universitas Sumatera Utara, Medan, Indonesia

12. Central Department of Microbiology, Tribhuvan University, Kirtipur, Nepal

Abstract

Background: The COVID-19 pandemic and resulting restrictions, particularly travel restrictions, have had significant impact on the conduct of global clinical trials. Our clinical trials programme, which relied on in-person visits for training, monitoring and capacity building across nine low- and middle-income countries, had to adapt to those unprecedented operational challenges. We report the adaptation of our working model with a focus on the operational areas of training, monitoring and cross-site collaboration. The new working model: Adaptations include changing training strategies from in-person site visits with three or four team members to a multi-pronged virtual approach, with generic online training for good clinical practice, the development of a library of study-specific training videos, and interactive virtual training sessions, including practical laboratory-focused training sessions. We also report changes from in-person monitoring to remote monitoring as well as the development of a more localized network of clinical trial monitors to support hybrid models with in-person and remote monitoring depending on identified risks at each site. We established a virtual network across different trial and study sites with the objective to further build capacity for good clinical practice–compliant antimalarial trials and foster cross-country and cross-study site collaboration. Conclusion: The forced adaptation of these new strategies has come with advantages that we did not envisage initially. This includes improved, more frequent engagement through the established network with opportunities for increased south-to-south support and a substantially reduced carbon footprint and budget savings. Our new approach is challenging for study sites with limited prior experience but this can be overcome with hybrid models. Capacity building for laboratory-based work remains difficult using a virtual environment. The changes to our working model are likely to last, even after the end of the pandemic, providing a more sustainable and equitable approach to our research.

Funder

Australian Academy of Science

Bill and Melinda Gates Foundation

National Health and Medical Research Council

Publisher

SAGE Publications

Subject

Pharmacology,General Medicine

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