Empower Clinical Trial Patients with Conversational AI

AI-powered assistance for seamless clinical trial experiences

Patient-Centric Trial

Respond to the study subjects' questions 24/7 and maximize satisfaction

Increase retention rates, reduce drop-out and trial costs

Reduce the workload on the clinical trial study team

Trial Success
Support Study Team

Equip participants with Conversational AI

The patients have numerous questions during clinical trials that need to be timely answered. We developed an AI-powered chatbot that resides on the patient’s own smartphone and provides essential information

Make your trial Patient-centric
Maximize Patient Satisfaction

After signing ICF, enrolled participants still have the post-enrollment inquiries. Study subjects often lack full information about the trial. Lack of constant awareness can impact their decision to stay enrolled and result in dropping out of the trial

Key Features

AI assistance for clinical trial participants available 24/7 to enhance their experience and engagement.

Get insight from your study that you did not knew about!

This tool allows Sponsors/CROs to analyze the types of questions participants ask the chatbot. By identifying trends and recurring inquiries, this data can be used for the clinical trial improvements

Customized Natural Language Processing (NLP)

This conversational AI model can be trained with the project-specific data and answer any questions that may arise during the trial

How it works?

Our AI model already has a deep knowledge of the medicine and specifically - Clinical Trials. We will customize our AI model on your specific clinical trial
The following documentation should be provided from the Sponsor:

1. Informed Consent Form (ICF)
2. Participant Communication Materials

Optional:
1. Investigator’s Brochure (IB)
2. Non-confidential sections of the
Study Protocol
3. Case Report Forms (CRFs)
4. ePRO Templates
5. Insurance Template

We know why we do that

We have conducted quantitative research on the US market. See the insights!

  • 30% of participants are shy about asking questions to the study team

  • 57 % think they’re asking “silly” questions

  • 80 % contact the study team remotely

  • 43 % don’t always receive timely responses

  • 65 % often ask questions that were already explained

  • 46 % do not read the informed consent form thoroughly

Included/Excluded Features

AI assistance for clinical trial participants available 24/7 to enhance their experience and engagement.

No Real-time Decision Support

Our platform supports participants by providing general trial-related information, but it does not replace medical staff or real-time assistance. It is not for medical advice - urgent concerns must go to the trial team

Zero Hallucination

Our AI utilizes NLP to understand patient questions and match them to the most relevant information from trusted sources. It does not interpret or alters the information. This approach prevents AI bias and misinterpretation of responses.

Let's be more specific!

You can view a breakdown of our capabilities here:

What we can:
What we can NOT:
  • Replacing the Study Team’s Judgement

  • Medical Interpretation or Decision-Making

  • Real-Time or Emergency Support

  • Educating on Clinical Trial Concepts

  • Enhancing Informed Consent Understanding

  • Clarifying Study Procedures and Expectations

Data Privacy and Compliances

We don't train our models on your data. This model is already well trained. We just customize it according to your specific trial

Our platform adheres to the requirements of the HIPAA, ensuring the confidentiality and security of your protected health information

Our platform meets the FDA's 21 CFR Part 11 requirements for electronic records, ensuring the reliability of your data

Get in Touch

We’re here to assist you with any inquiries about Triamel AI and our services. Reach out today!

Connect

+995 579 988 998

Support

hello@triamel.com