Accelerating The Cure
Now is the time to rethink how research sites
and patients manage their study journey
Now is the time to rethink how research sites
and patients manage their study journey
As a patient, I want to understand my options better while becoming part of a clinical trial. It would be great to have something to reference and resources for this!
I would like to reference my consent form. I wish there was a way to electronically store my consent and access it when I want.
As a patient, I wish I had an electronic system to help me keep track of all the information I’ve received for this study, like help navigating the trial process, organizing my visit calendar, and what to expect at each study visit.
As a patient, getting to and from my doctor visits can be a challenge; so staying with my clinical trial can be difficult. I’d love a way that would make this easier or more automatic for me.
With my day-to-day schedule it can be hard remembering to take my study medication. It would be nice to receive a simple daily reminder.
I would love to provide feedback on my experience participating in a clinical trial. I wish there was an easy way for my voice to be heard.
ClinOne eConsent is highly flexible and can accommodate a broad range of signers, including those who consent remotely
Video eConsent brings trials to the patient, combining video conferencing and e-signature in a single application. Patients, caretakers, co-parents, sites and translators can all be involved.
Entire consent process is documented, generating a comprehensive consent log including ID’ing participants, steps taken, duration on each page and questions encountered
Consent log is automatically added to final page of ICF
Patients can receive their signed consent via secure email or by downloading and printing
KnowledgeBase provides patients and caregivers access
to important information about their disease, study
details and frequently asked questions.
As a patient, I want to understand my options better while becoming part of a clinical trial. It would be great to have something to reference and resources for this!
ClinOne provides patients with a digital concierge to
manage their clinical trial experience, assuring greater visit compliance and retention. They can manage their visits, get guidance on travel options with Google Maps integration, get
specific research visit details, as well as study specific alerts and
reminders through the app.
ClinOne and Uber Health have partnered to provide patients with the option of utilizing Uber’s ride-sharing application to get to and from visits
Seamless integration with our Digital Concierge suite allows patients to simply request an Uber for each of their visits, with the ability to schedule in advance
When patients are picked up by Uber, family and site staff are notified via text and email alerts
Patients receive dosing reminders and send confirmations to/from their mobile phone, wearable device, laptop or tablet
Patient reminders are sent specific to the protocol treatment schedule, time zone and in the patient’s native language
eDosing Manager records when reminders are sent and read, and when confirmations are sent and received
Sites receive weekly reports with summary of their patients’ dosing compliance, allowing for proactive adherence management.
Patient Voice allows patients to provide personalized feedback about their clinical trial experience
Patient Voice can distribute the patient surveys at predetermined times throughout the studies
ClinOne provides trending reports with predictive indicators of patient compliance and risk of non-medical indicators which may impact study withdrawal
It benchmarks patient satisfaction across research sites to help identify sites that are fully engaged with their patients or which are underperforming
Sponsors and CROs can quickly intervene and provide greater support, focusing their attention on areas where patients have reported dissatisfaction
Meets or exceeds enrollment goals for sites, efficiently and cost-effectively
ClinOne’s extensive network of specialty physicians is part of this offering for all ClinOne trial sites
Bi-monthly emails ('Dear Doctor' letters) are sent to targeted specialty providers
Ongoing referral support, continuously customized to each trial site's needs
A single study can require research sites to perform 400 to 800 investigational procedures per patient, or as many as 140,000 procedures if they have enrolled 3 patients per study across a portfolio of 30 to 60 studies.
ClinOne provides a powerful workflow management tool to manage every single, individual procedure to mitigate the potential of costly protocol deviations.
ClinOne unifies research sites through its confidential digital community.
The technology provides sponsors with a platform to effectively communicate with hundreds of research sites and thousands of users across the globe.
The community can build an ongoing list of frequently asked questions for research sites to utilize as a resource.
Patients and their loved ones must feel empowered and fully connected while participating in a clinical trial
Patients and families need a new approach to rethink how connected and engaged they are within a clinical trial
Provide complete transparency to sponsors about their patients' experience and journey
By giving patients a way to provide constant feedback, they can become an active participant throughout the trial process.