As the landscape of clinical trials evolves towards more inclusivity, diversity, and complexity, patient engagement is becoming more crucial than ever. Patients are the heart of clinical trials, and their participation can make a significant difference in the success of the trial. Therefore, it's essential to improve patient engagement to achieve better treatment outcomes, patient satisfaction, and health, as well as increased enrollment, reduced dropout rates, and more cost-efficient trials.
Viedoc Me is a user-friendly cloud-based application that enables trial participants to report their own data via their smartphones, tablets, or computers. It fosters seamless communication between patients, investigators, and sponsors in real-time, promoting collaboration, trust, and long-term engagement. With Viedoc Me, patients can quickly and easily submit ePRO, eCOA, and eConsent data, ensuring more accurate and reliable results. The clear, easy-to-use, and top-modern interface of Viedoc Me reduces barriers to entry and encourages patients to persist throughout the trial.
"Viedoc Me is very complete and easy to set up. It has allowed us to do things that were not possible with other systems," says a verified user and SME on G2. "I have experienced Viedoc Me across various projects. The system is really user-friendly. On each project, I've been amazed by the flexibility and the agility of the Viedoc team," adds Isabell G, Clinical Research Manager, Pharmaceuticals on Capterra. When the patient data is collected, Viedoc Me is seamlessly integrated into Viedoc's suite of clinical trial management software, facilitating more efficient trials.
The importance of patient-centered outcomes in clinical trials has been increasingly recognized in recent years. A study published in the Journal of the American Medical Association found that trials that focused on patient-centered outcomes were more likely to report positive treatment effects than those that did not. In addition, patients who participated in these trials reported higher levels of satisfaction with their care and were more likely to adhere to their treatment plans. This research highlights the need for patient engagement in clinical trials and the importance of patient-centered outcomes in achieving better treatment outcomes and patient satisfaction.
As a result, there is a growing focus on patient-centered outcomes from sponsors and regulatory agencies, driving the need for improved patient engagement in clinical trials. Viedoc Me is committed to addressing this need by providing a user-friendly platform that enables patients to report their own data and communicate with investigators and sponsors in real-time, ultimately leading to more accurate and reliable results.
With a commitment to advancing patient engagement in clinical trials, Viedoc recognizes the role of digitalization in making it easier for patients to participate in research. Digitalization, and modernization at large, is playing a crucial role in improving patient engagement. With the increasing use of Real-world Evidence (RWE), traditional data is now complemented to capture long-term effects and safety of treatments.
At Viedoc, we understand that removing participation and engagement barriers is vital to achieving successful patient engagement. We design our platform's UI to be intuitive and make data engaging and even fun to participate in. Our smart functions and day-to-day notifications for patients help encourage them to report data in a consistent and timely manner, fostering real-time communication between patients, investigators, and sponsors, and promoting collaboration, trust, and long-term engagement. With Viedoc Me, we strive to provide a seamless experience, removing barriers and providing a user-friendly cloud-based application that makes it easier than ever to participate in clinical trials.
With Viedoc Me, we strive to deliver the best patient engagement solution available. By collecting data directly from patients, eliminating transcription errors, and enabling real-time communication between patients, investigators, and sponsors, we provide a streamlined process that ensures the most accurate and reliable results. If you're a CRO, data manager, sponsor, or clinical trial professional, now is the time to take a closer look at Viedoc Me. It's as easy to learn as it is to use.
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"Viedoc makes building a study easy and fun. It doesn't require extensive coding knowledge; it's quick to get in and start working."