Clinical Research in Plain Language
ResearchClaro is a plain-language clinical research education resource designed to help people understand what research means for them. Our goal is to make research information clear, accessible, and empowering for communities.
About
I’m a clinical research professional with over a decade of experience working behind the scenes of research studies — from recruitment and consent to participant education and community engagement.
Throughout my career in Philadelphia and surrounding communities, I’ve worked closely with families, caregivers, and Spanish-speaking participants across studies in behavioral health, HIV, early childhood development, and public health. I’ve seen firsthand how research is often explained in ways that feel overwhelming, rushed, or unclear — and how that lack of clarity can lead people to reject research immediately, simply because they don’t know what questions to ask.
ResearchClaro was created to change that.
This space exists to explain clinical research in plain language, empower participants to understand their rights, and help families make informed decisions — without pressure. We are an independent educational resource, not affiliated with study teams and not involved in recruitment. Our only goal is clarity, confidence, and informed choice.
Everyone deserves clear answers when it comes to their health and participation in research.
Our Services
Plain-language education for participants and families
Understanding consent, rights, risks, and benefits
Support for English- and Spanish-speaking communities
Esta guía explica la investigación clínica en un lenguaje sencillo y cotidiano para que los participantes y sus familias puedan entender a qué se les invita a participar. Incluye información sobre el consentimiento, los derechos de las personas participantes, los riesgos, los beneficios y las preguntas más comunes. Esta guía está diseñada para ayudarle a sentirse informado(a), con confianza y con el poder de tomar la decisión que sea correcta para usted.
This guide explains clinical research in simple, everyday language so participants and families can understand what they’re being invited to join. It covers consent, participant rights, risks, benefits, and common questions — without pressure or medical jargon. Designed to help you feel informed, confident, and empowered to make the decision that’s right for you.
Recruitment & consent best practices
Communicating research clearly and ethically
Improving participant understanding and trust
