Video calling in clinical trials refers to the use of video conferencing technology to conduct remote study visits with trial participants. Rather than meeting in person at the study site, participants and study staff connect through a secure video through the Your Research Portal allowing for real-time communication and interaction.
Your Research video calling software facilitates remote communication and virtual interactions between study participants and healthcare professionals, enabling convenient and efficient data collection, monitoring, and patient support without the need for physical visits to healthcare facilities.
Conduct remote assessments and data collection, allowing participants to conveniently and safely participate in the study from their own homes or preferred locations, reducing the need for in-person visits and potentially improving patient recruitment and retention rates.
Video calling software allows for live, face-to-face interactions between study participants and healthcare professionals, enabling effective communication, discussion of symptoms, provision of instructions, and addressing questions or concerns in real-time.
Video calling software ensures data privacy and confidentiality by providing secure, encrypted connections for transmitting sensitive medical information during tele-health visits, ensuring compliance with privacy regulations such as HIPAA.
Your Research video calling software integrates with electronic health record (EHR) systems, clinical trial management systems (CTMS), and other digital platforms, enabling seamless exchange of patient data, scheduling of virtual visits, and documentation of visit outcomes, enhancing overall efficiency and data accuracy in clinical trials.
Eliminate the need for commuting and waiting times, allowing for efficient data collection and real-time interaction.
Video calling software enables participants to attend study visits remotely, eliminating the need for travel and reducing the burden of physical clinic visits, making it more convenient for patients, especially those with mobility or geographical limitations.
Virtual study visits can enhance patient engagement and retention by providing a more patient-centric approach.
Participants may feel more comfortable and involved in their own environment, leading to increased compliance, higher retention rates, and improved overall study outcomes.
Conducting virtual study visits can significantly reduce costs associated with site visits, including travel expenses, site staffing, and infrastructure requirements.
It also saves time for both participants and researchers, eliminating the need for commuting and waiting times, allowing for efficient data collection and real-time interaction between participants and study personnel.
Discover how our consent module optimizes clinical trials and academic research, enhancing data collection and participant comprehension.
With Your Research, you have the flexibility to utilize stand-alone modules, integrate them with your existing software vendors, or connect them to other modules within Your Research to enhance the participant journey.
Contact us and we will be happy to show you how Your Research makes a difference in conducting clinical research, making research more efficient and personalised for everyone involved.