Unlocking the Power of Patient-Centric Research

Patient Feasibility Study

At Link2Trials, we believe that the heart of every successful clinical trial is the patient. That’s why we’ve developed our Patient Feasibility Study. This will ensure that your trials are not just compliant, but also compassionate, considerate, and patient-focused.

Our Approach

Our Patient Feasibility Study service offers a comprehensive analysis of your trial from the patient's viewpoint. We delve into the heart of patient concerns, needs, and preferences to bring you insights that transform the traditional clinical trial into a patient-centric journey.

Inclusion Criteria Analysis

We evaluate the relevance and clarity of the inclusion criteria from the patients' perspective. This helps us to ensure that the criteria effectively communicate the study's eligibility requirements and that patients understand whether they qualify to participate.

Patient-Driven Trial Design

We go straight to the source—patients themselves—to solicit their views on your trial's framework, timeline, and logistics. Their direct input is crucial in shaping a trial setup that meets their expectations and encourages their participation.

Comprehensive Documentation Review

From the landing page to the Informed Consent Form (ICF), we gather feedback straight from patients to confirm that every document is not just readable but relatable. We ensure these critical materials are crafted with the utmost regard for patient comprehension and comfort.

Why Choose Patient Feasibility Study?
  • Tailored Feedback: Direct from diverse patient populations to refine your protocols.
  • Enhanced Protocols: Reimagined with patient-centric perspectives for greater engagement.
  • Clear Communication: Ensuring that every document speaks to and respects the patient.
  • Empowered Decisions: Giving patients the information they need to participate confidently.
  • Improved Experience: Shaping trials to be more accommodating, understanding, and patient-aligned.
  • Faster recruitment
  • Optimized study adherence profile
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