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SMART Designs: Bridging the Gap Between Clinical Trials and Practice in Infectious Diseases
Lara Maleyeff1, Erica E M Moodie1, Shirin Golchi1
1Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montréal, Quebec, Canada.
None:
Traditional randomized controlled trials often fall short in addressing the specific needs of clinical practice due to their one-size-fits-all treatment approaches. Sequential multiple assignment randomized trials (SMARTs) offer a dynamic and adaptive approach, allowing for multiple randomizations based on patient responses and evolving conditions. SMARTs enable personalized treatment pathways, such as in the trial for antiretroviral therapy in South Africa, which adjusts treatment based on patient outcomes. Despite these advantages, the use of SMARTs in infectious diseases remains limited. Greater adoption of SMARTs could promote more personalized treatment approaches, improve flexibility in response to public health needs, and enhance the effectiveness of interventions. However, challenges such as recruitment and increased expertise needed for more complex analyses must be addressed. Additionally, combining SMARTs with other adaptive designs could further improve the relevance and outcomes of clinical research.
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