The research industry is changing rapidly and embracing patient-centric practices. When COVID-19 restrictions came into effect, a large part of the industry moved to remote modalities for the sake of research continuity. With these remote practices, researchers became more conscious of the participant experience and prioritized the participants’ comfort.
That said, simply moving to remote research isn’t enough to make your study patient-centric. In fact, you need to have an intentionally designed study that uses remote functional tools to facilitate the participants. This will make it easier to recruit participants and speed up the research’s pace.
One remote tool that goes hand-in-hand with patient centricity is eConsent. But what is the connection between the two? Keep reading to find out.
What’s a Patient-Centric Study?
Patient-centric studies focus on refining the patient experience so that they’re more willing to participate. When a research organization embraces patient-centricity, they have to work on a few components to get there. Here are all the components of patient centricity:
- Study Design: The entire study should be planned in a way that the participants’ comfort is prioritized from their recruitment until the very end of the study.
- Retention: The study should work around the participants’ schedule. If you can find ways to bring the trial to them instead of bringing them to the trial, you should do it. The best way to achieve this is through remote modalities.
- Communication: Consistent communication can create an overall positive experience for the participants. When communicating with the participants, you should keep the communication direct, honest, easy to understand, and thoughtful so that there’s healthy dialogue.
How is eConsent Connected to Patient Centricity?
One of the ways to become more patient-centric right from the beginning is to use eConsent for the research. This electronic consenting tool helps research organizations educate their patients, evaluate participant comprehension, and improve compliance. This tool allows researchers to use different learning styles and increase their communication options.
Here are all the ways eConsent can help you become more patient-centric:
- It improves patient comprehension as it can be deployed on the participants’ own devices, which they’re already familiar with.
- Participants can easily review all the study material whenever they want and discuss it remotely.
- They can read all the stipulations of the consent thoroughly and on their own terms and only sign when they’re ready.
- eConsent also uses interactive multimedia elements that improve participants’ comprehension.
- This tool has a glossary of all the terms and their meaning to help participants understand the specifics of the trial.
Needless to say, all these things have a direct effect on trial success as researchers can avoid many issues and stay compliant when using eConsent.
Get Top-Rated eConsent Tool for Your Research
If you’re looking to make your research more patient-centric, starting with eConsent is the best way to achieve this. ClinicalPURSUIT has a robust, HIPAA-approved eConsent tool that will streamline your research and make it easier for you to recruit participants.
We’re a clinical trial technology company with comprehensive clinical trial data management solutions and tools to ensure patient-centric clinical trials. Our products include EDC software, SDVs, eCRFs, clinical trial remote monitoring, and more.
Get in touch with our team to learn more.
