The Exco InTouch Retention and Compliance solution is powered by InTouch Clinical, our industry leading and award winning communication product.
Using a unique combination of Internet and Mobile Phone technology, our patent pending methods of providing regulatory compliant messaging services, enables InTouch Clinical to automatically schedule and deliver cell phone based, study specific text messages direct to the patient in their preferred language and local time zone.
Sites
We all recognise that site staff today are extremely busy and with this in mind we offer a straightforward mechanism for the sites to enrol patients, manage communication and review patient compliance information.
Following simple training, site users access the secure Exco InTouch website using a unique username and password. Patients are enrolled quickly and easily using their subject ID, cell phone number and first visit date, the system then calculates the patients' ideal visit schedule and assigns appropriate messaging to be sent at the required study milestones.
This schedule for each patient can be easily edited to reflect both patient and site preferences with reminders to stay within visit windows. Messages are sent either via SMS text message to the cell phone or email to a nominated account.
It is important to provide features that help the site with their work processes. Exco InTouch have built in several features that help the site manage patients and their own administration time more effectively:
Patients
As with all technology solutions, for it to be a successful, the end user must be satisfied. With all Exco InTouch solutions, during the requirements and design phase, we gather as much information as possible about the typical patient and site users who will interact with our service.
The system can be designed to take multiple phone numbers if required so that in the event that the patient does not attend the visit or cannot be contacted, the secondary contacts or careers can be approached.
Once enrolled, patients will begin to receive SMS reminders about study milestones. As this information is delivered via SMS, training of patients is minimal and, in most cases not required.
All SMS Text Messages are scheduled and managed via our ATLAS SMS gateway - a global, regulatory compliant, enterprise SMS text messaging application that works in conjunction with InTouch Clinical.
Using validated cellular networks, ATLAS schedules, sends and tracks delivery of SMS text messages worldwide. Currently ATLAS connects to over 750 mobile networks in 196 countries providing a reliable and robust mobile network for sites and patients to connect with. All SMS text messages transmitted by InTouch Clinical are subject to a full audit trail and receipt generation mechanism which means we know when a text message has been successfully received by a patient.
Unlike pre-configured static reminders in other systems, SMS text message reminders are delivered from a central server using NTP (Network Time Protocol). This ensures they will be delivered at the correct time and we can track the successful delivery, rather than relying on a local clock setting of the device.
Exco InTouch uses only approved and audited mobile networks in conjunction with our ATLAS software. This is essential to guarantee against spam messaging and also in protecting patient's confidentiality. For example, in the USA, messages must be sent through a dedicated mobile shortcode which is controlled by a registered company and approved by each cellular network independently. This global infrastructure took over 18 months to develop and validate and we are proud to offer this capability to our clients.
Our solution is designed to be compliant with the regulatory requirements of the FDA and HIPAA concerning patient privacy and data protection. The solution is approved by ethics and IRB's globally and is proven to be effective in patient management by automating text message communication.
InTouch Clinical is configured by the Exco InTouch project delivery team to match the requirements of the protocol and other trial milestones / deliverables. Our project team guide clients through system set up study conduct to ensure the system is utilized to the full potential.
Once the system is live, patients are enrolled by trained site staff via a simple and secure website which creates no additional workload and provides a useful reference point to help site staff manage their day to day tasks.
Patient communication is automated throughout the trial, a typical retention and compliance program will employ one or a combination of the following types of messages:
How can we help your study to succeed?
When you feel you have all the information you need then we are always happy to discuss your study design and provide our recommendations. We can even show you a live demonstration so you can witness firsthand the benefits of inTouch Clinical.
Kick off only takes two hours and we do nearly all the work. We manage the adoption of the tool and you only need to invest one man day of effort from start to finish. We will train and provide eLearning, allowing you rest easier because the subject and site compliance is not left to chance.
To book a demonstration, request a proposal or to speak to an Exco InTouch expert, please use the "I like what I see" form on the right of this page and we will contact you shortly.
Want to see InTouch Clinical in action? If you have a username and password, click the link below to enter the live demo.
Don't have a login? Please use the 'I like what I see' form below and request access.
To see how Exco InTouch can help, use the quick form below to talk to an expert, book a demo or request a quote.
Please find below a selection of relevant, downloadable publications.
Retention & Compliance Summary
Cell Phone technology in Pharma
To see how we have helped Clinical Study success, please read one of our case studies below.
Enhancing subject recruitment, improving subject compliance & retention & facilitating data capture direct from trial participants
Enhancing clinical trial recruitment, allowing sponsor companies to reduce timelines & ultimately bring new drugs to market faster
A simpler, more efficient way to gather PRO data from subjects, caregivers & sites, that is quick to set up & easy to use by all participants