the challenge
Are you developing clinical trials without incorporating true patient perspectives from the start?
Many research teams design protocols based on clinical expertise alone, missing critical insights about what matters most to the people who will actually participate in the trial.
Regulatory bodies and funding agencies increasingly require evidence of meaningful patient involvement throughout the research process, not just during recruitment.
Our patient engagement specialists facilitate structured, productive group discussions that capture invaluable insights from those with lived experience of your target conditions.
We offer a completely free introductory discussion call to address your individual needs. Sign up by filling in the quick form here:
at nclusiv we...
- Facilitate productive patient discussions — Our skilled moderators create environments where patients feel comfortable sharing honest feedback about research designs and materials.
- Recruit diverse, condition-specific participants — We access our extensive database to assemble representative patient groups with relevant lived experience.
- Structure discussions for maximum insight — Our proven methodologies ensure sessions generate actionable feedback rather than unfocused conversations.
- Translate patient input into actionable recommendations — We don't just relay opinions; we provide structured reports with clear implications for your trial design.
- Enhance protocol development — Identify potential barriers to participation and adherence before they impact your trial timeline.
- Strengthen ethical foundations — Demonstrate meaningful commitment to patient-centered research approaches.
- Support regulatory requirements — Generate documentation of patient involvement for RECs and funding bodies.
- Improve recruitment and retention — Design trials that better align with patient needs and preferences from the start.
