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Clearly Communicating Clinical Trials (C3T)

C3T was built to address a clear gap: the lack of health literacy integrated in clinical research and trials. Clinical trials have the potential to advance medicine and improve lives, but many studies fail to engage the people who could benefit most because the information is too complex, inaccessible, or disconnected from real-world needs. Health literacy can bridge that gap. That's where we come in. 

Complex science made clear.

Through tailored health literacy strategies, we help research teams communicate more clearly, build trust, and foster meaningful participation. From study design and participant materials to consent forms, study updates, and summaries, we ensure every point in the process is understandable, relevant, and actionable.

Recruitment

Health literate recruitment materials engage everyone and encourage diverse representation

Consent

An understandable consent process is essential to true and legal informed consent

Retention

Clear data collection forms ensure accurate data – no matter if the trial is local or decentralized

Results

Patient-friendly summaries help patients understand their role and encourage future participation

Evaluation

Constant collection of insights ensures all research is grounded in the patients’ values

Communication

Staff communication strategies can facilitate meaningful participation for all involved

How we partner

Our team works alongside yours to translate key details and data into clear, accessible, and usable recruitment materials, consent forms, and summaries that convey complex information with accuracy and confidence. Throughout the process we stay attuned to regulatory requirements and timelines — helping you meet them without sacrificing clarity, equity, or participant understanding.

Valued stakeholders

We value the importance of the audience's role in making meaning of and their expertise in their own lives. We work to value all stakeholders in the complex process of connecting science and community.

Confidentiality

We operate in a virtual, secure environment while maintaining close contact with your clinical disclosure, operations, medical writing, and legal review teams. We uphold strict confidentiality at every step.

Flexible formats

We provide materials in a variety of formats, including print, digital, video, social graphics, and templates. Our flexible approach allows us to integrate seamless into your process, ensuring compatibility at every stage.

Quality deliverables

We use evidence-based approaches to health literacy and plain language to translate complex methods and results into effective communication that meets study team and audience needs.

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Whether you're designing a new clinical trial, conducting community-based research, or improving patient-facing materials, we bring the expertise to make your research more effective.

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