mPRO ™ enables researchers and their staff to review and analyse real-time information. It can also be a quick and simple communication tool with trial subjects (where permitted).
Fully customisable diaries, using adaptive branch logic are downloaded to mobile phones. Subjects answer diary questions via the mobile phone and the data is automatically sent wirelessly to a secure server. Researchers and staff can instantly access subjects’ real-time information and begin to quantify and qualify study trends and analysis.
Benefits
Fast rollout – the use of mobile phones ensures setup and roll out phases are FAST (sent to subjects within days of diary customisation and completion). Quicker trial implementation means quicker results.
Real time analysis – ensures high compliance, real time outcome data and statistical significance, reducing important timelines between drug discovery and launch.
High compliance – the user of familiar, comsumer friendly technology supported by real time subject monitoring leads to very high subject compliance rates typically in excess of 90%.
Secure messaging – researchers and staff can communicate securely to their study subjects through t+ Clinical’s encrypted messaging system.