Why is Virtual Clinical Trial Considered the Future of Clinical Trials?
Virtual trials use a web-based platform to coordinate all requirements and bring clinical trials to patients’ homes. Experts in the field offer Veristat clinical trial consulting services to meet the various trial needs throughout the trial lifecycle. The last few years have seen the substantial development of virtual clinical trials, thanks to digitalization and technical improvements. Virtual clinical trials can take advantage of new technologies to boost patient satisfaction, operational efficiency, and the adaptability of clinical research. There are drawbacks to virtual trials, but the many advantages outweigh them. Evidence suggests that conducting trials virtually leads to
Improved patient engagement
The time and money saved from not having to physically travel to trial sites is a major selling point of virtual trials. Patients have easier access to care, especially if they have mobility challenges, and are more comfortable doing so. What’s more, patients can voluntarily participate in virtual clinical trials from the comfort of their homes. Furthermore, more doctors and clinical trial staff have access to a larger pool of patients.
Real-time and more detailed data collection
Mobile devices, wearables, and home monitoring systems are commonly used in virtual trials to collect continuous data from participants in near real-time. Normally, information is collected at regular intervals at investigator sites during clinical trials. Thanks to advancements in tracking technology, businesses in the life sciences can now collect vast amounts of data without physically meeting with their clients. Virtual trials are predicted to evolve into a new and powerful method of data collection. The study is useful for data collection since it improves safety evaluations for new endpoints and measurements while still meeting deadlines.
Improved patient enrollment and retention
Virtual clinical trials have the potential to improve patient enrollment and retention. The key to successful retention is employing strategies that keep patients interested and involved throughout the study. In this case, you must focus on what the patient is going through and try to empathize with them. Factors like required online meetings that occur at predetermined intervals increase dropout rates. Virtual trials could lessen such responsibilities by focusing on trial participants via telehealth services, including wearable devices and remote visits to obtain virtual clinical data. But the trial designs must use these digital tools to meet stringent patient safety standards.
Enhanced data diversity
Patients taking part in conventional clinical trials are required to physically travel to and from each site. However, modern advances in technology have led to the development of virtual clinical trials, which greatly reduce the impact of distance on the accessibility of scientific research for people from all walks of life. People from minority groups, the elderly, those living in rural areas, and so on are all included. This trial approach allows participants to collect a broader range of data to improve external validity.
Virtual trials use a web-based platform to coordinate all requirements and bring clinical trials to patients’ homes. Despite their drawbacks, virtual trials offer many advantages that researchers and pharmaceutical companies can make the most of as seen above.