Study Portal

Trial Design & Patient Management

The study portal is dedicated to study investigators and clinicians, supporting any type of study; from small investigator-driven studies, up to sponsor-based multi-centre, multi-lingual randomized studies.

The study portal offers advanced features for study management:  

StudyPortal

Capabilities

Group 225

Real-Time Access to data

Real-time monitor of your population's data from any device

 

Group 230

Scedulling of Messages

Schedule notifications for every important step of your clinical research so as to ensure your endpoints

 

Group 229

Population Behavioral Phenotypes

Unsupervised, automatic biomarker discovery in data and grouping of validated biomarkers into phenotypes

Group 233

Audit Log

Monitor the activity in the platform and application through the audit log

 

Group 226

User Roles & Permissions

Give roles & permissions to your research team

 

Group 231

Instant Notification

Instant notifications can be sent whenever it is needed in order to inform the patient about treatment updates or visits

 

Group 228

Chatbox communication

Investigator and subject can interact with a protocol assigned script

Group 234

Forms

All types of questionnaires can be designed and scheduled to be sent to patients on the ePRO app

Group 232

Reports & Analytics

Healthentia gives specific reports and analytics in customizable dashboards to view trial metrics the easiest way and have a clear view of population data to act upon

Group 227

Population Tagging & Dynamic Lists

Catalogue your patients and find them easy by their personal characteristics or the clinical research they participate

startscreen

Trial Design and management

Healthentia's integrated eCOA platform allows organizations to set up trials according to Protocol specifications and connect seamlessly with the ePRO and any wearable device given in the Trial. These are some of the key features:

Advanced Questionnaire builder and complex routing

ePRO questionnaire scheduler and messaging module

Auto-tagging subjects from questionnaire answers

Customizable Dashboards and BI tools for protocol endpoints

 

Subject management

Access your subjects lifestyle data and Outcomes

Healthentia's integrated eCOA platform allows organizations to set up trials according to Protocol specifications with the following key features

Follow protocol adherence real time

Get insights on protocol endpoints

Inform subjects on trial update

Unlock new insights from patient data

 

 

subjetctData
dashboard_stats

Population datapoints

Overview of a trial's key endpoints

In Healthentia we customize home dashboards related to the

Follow protocol adherence real time

Get insights on protocol endpoints

Inform subjects on trial update

Unlock new insights from patient data

 

 

Made for your Business

Have any question? Visit the contact page to reach out to us.

Healthentia medical device is a smartphone app for chronic disease patients and a clinical dashboard for healthcare professionals. Healthentia is offering advanced RPM features through its medical modules that empower patients with chronic diseases and contribute to better health outcomes. Its intended purpose includes the collection of physiological data, visualization and trend analysis, transmission of patient outcomes to healthcare providers, and the enabling of personalized interactions through a virtual coach. Further to the RPM features, Healthentia is addressing the root cause of chronic disease, the behavioral risk factors and through personalized virtual coaching, assists patients towards a lifestyle change.

Healthentia is also used for Decentralized Clinical Trials (DCT, leveraging best-of-breed of eClinical studies features, such as eRecruitment, eConsent, teleconsultation/ televisit, ePRO-IoT integration, and virtual coaching. Healthentia empowers patients and gives them an active role in taking trial’s actions, rather than bringing them to the trial sites; thus facilitating clinical trial optimization, accelerating trial processes, reducing drop-out and failure rates, and validating drug/intervention efficacy and effectiveness with Real World Data insights. Healthentia is used by Top5 Pharma and large hospitals and operates under the strict regulatory framework of Good Clinical Practice.