Fast-track your decentralised clinical trials or observational studies.
Combining ResearchAppTM , our patient-friendly app and Healthbit IQTM, our study management and intelligence dashboard.
The Healthbit IQ Clinical Trials Platform
Our powerful technology empowers researchers, enhances participant engagement, and accelerates medical research. With the Healthbit platform, we’ve done the hard work to bring you easy-to-use tools that integrate seamlessly together and allow you to setup, operate and monitor your study.
Whether you’re conducting decentralized, hybrid trials or observational studies; seeking to improve participant engagement in studies or seeking compliant data capture capabilities; we have you covered.
We’re making research smarter, faster, and more inclusive.
Our extensive SaaS platform facilitates the rapid customisation and deployment of the patient-friendly ResearchAppTM for decentralised trials and studies.
Capture everything: eCOA, ePROs, connected device data, symptoms, adverse events, health and lifestyle indicators, resource utilisation and more. Data is seamlessly captured, structured and made available in reporting dashboards. View insights, download data or integrate it via the API.
Accelerate study design with our extensive library of clinically validated ePRO/eCOA surveys, assessments and health trackers, or simply design your own.
Use the ‘drag and drop’ features to build and test custom surveys with advanced features, including:
Validation & Branch Logic
In-line calculations and scoring
Image and video capture for AI driven data processing.
Put participants at the centre of the consent process and ensure study protocol compliance.
By utilizing the e-consents feature, researchers can streamline the consent process, reduce administrative burden, enhance participant understanding, and maintain compliance with regulatory standards. It promotes a participant-centric approach, improves data management, and ensures the ethical conduct of clinical trials.
Our e-consents feature adheres to regulatory standards and guidelines for electronic consent processes. The platform incorporates security measures to ensure data privacy, authentication of participants, and compliance with applicable data protection regulations.
Participants can access and review the consent forms through the Research App. This promotes transparency, participant engagement, and informed decision-making.
The built-in randomization module streamlines the randomization process. Researchers can easily configure randomization parameters within Healthbit IQ, allowing for efficient and automated allocation of participants to treatment groups. This helps maintain the scientific rigor of the study and enhances the validity of the research outcomes.
By enabling the randomization module researchers can eliminate the need for external statisticians solely for the purpose of randomization. This results in cost savings for research teams, allowing resources to be allocated to other important areas of the study.
Have your own data statistician?
No problem import randomisation assignments from popular statistical software packages such as Stata.
Randomisation methods include Simple Randomization, Stratified Randomization, Block Randomization, Cluster Randomization, Minimization and Stratified Blocked Randomization.
The choice of method depends on the study design, research question, and specific requirements of the study protocol.
Decentralizeed trials offer rapid patient data collection reducing time and cost and accessible to a more diverse participant base.
The platform has a versatile participant enrollment form that can be made publicly available (or password protected) so potential candidates can be screened for inclusion.
Partnering with patient support groups
Medical Research Charities and patient groups are often the source of unparalleled knowledge and information on specific conditions, and in many instances act as an invaluable and trusted intermediary between patients and the healthcare system.
We work with Patient Support Groups to grow their patient base and quickly build an organised patient registry. Data collected can contribute to a better understanding of the disease and help drive recruitment for clinical trials.
Rarer conditions affecting fewer people worldwide or localised conditions in certain geographical areas (which are often overlooked) – will benefit immensely from having a greater pool of participants to analyse and gain insights from.
Research App is a powerful feature of our platform that empowers researchers to create a tailored and engaging mobile experience for trial participants.
You’re in control of everything from branding, consent screens, layouts and surveys.
Design custom surveys with our ‘drag & drop’ tools or select surveys to use from our extensive library; diaries, ePROs/eCOA, QoL, symptoms, health indicators, lifestyle, exercise, and more.
Real-Time data collection and monitoring
Integrating medical devices enables seamless data collection in real-time. By connecting with wearable devices, sensors, and other medical devices, our platform can capture objective measurements such as heart rate, blood pressure, glucose levels, activity levels, and more. This real-time data provides researchers with up-to-date and accurate insights into participants’ health status, improving the overall quality and timeliness of data collection.
This reduces the reliance on self-reported data, which can be subject to recall bias and variability. This enhances the integrity and validity of the trial data, leading to more robust and trustworthy research outcomes.
Investigators can utilise the Televisits Engine to communicate with participants while collecting eCOA endpoint data.
Facilitate telemedicine visits and electronic Clinical Outcome Assessments (eCOA) through our integrated platform. Conduct virtual visits, capture patient-reported outcomes, and enhance the flexibility and convenience of participant engagement. Save time, reduce costs, and improve overall participant experience with seamless televisit and eCOA capabilities.
Personalized and adaptive interventions
Real-time data enables personalized and adaptive interventions based on individual participant needs. Researchers can monitor participants’ health trends and remotely provide tailored recommendations, interventions, or adjustments to treatment plans. This personalized approach improves participant outcomes and allows for more responsive and individualized care.
Unlock the power of your trial data with our advanced analytics and visualization capabilities. Gain actionable insights, identify trends, and visualize data patterns through interactive dashboards and reports. Our data analytics tools help researchers make informed decisions, drive evidence-based conclusions, and accelerate the translation of research into clinical practice.
Customisable dashboards with rich interactive reports and structured encoded data (SNOMED CT\MedDRA) give you increased efficiencies.
Data can be exported or accessed via the API in real-time.
API built for developers by developers.
Easily Customise App Features, Branding & Menus
Empowering researchers to create a tailored and engaging mobile experience for trial participants:
Tracker Update Reminders
Patient Health Record
Medication Adherance Engine
Forums \ Support Tools
Automatic Study Invites
Data Location for Cloud Storage (UK, US, EU)
Customisable Research App
You’re in control of everything from consent screens, layouts and surveys.
Maintaining Compatibility with Global Standards
We support a number of global dictionaries and standards to optimise data interpretation, compatibility and interoperability, such as SNOMED-CT, OMOP, CDISC, FHIR and others.
Configure and design your own branded charity app that empowers patients and their carers. Powerful tools offer condition self-management, health insights, disease education and peer to peer conversations.