Clinical trials recruitment and retention of volunteers / subjects for medical research - Link2Trials Accelerating Clinical Research

Creating the best possible patient experience in clinical trials extends beyond the initial start and end dates. It's an ongoing process that begins with trial preparation and concludes with sending the trial outcome/results and a comprehensive and personalized thank you to all enrolled participants.

By taking the patient perspective (and perception) as the starting point, Link2Trails empowers you to enhance patient experience throughout the trial cycle. We can help you optimize your protocol, develop an effective e-consent process, identify, recruit and pre-select eligible participants promptly, and provide personalized support to boost adherence.

Patient Feasibility Study

We have extensive experience in recruitment and working with investigators, research sites, and pharmaceutical professionals. We can help you to fine-tune your study protocol for enhanced patient recruitment and adherence.

Patient recruitment & Pre-qualification

Being specialized in patient recruitment services, Link2Trials is always challenged to find the best way to the hearts and minds of patients. This is why from the first day we started offering our services and long before anyone talked about patient centricity, we were already focused on how to continuously improve the patient’s experience with recruitment for clinical trials.

e-Consent

Our e-consent module will increase the patient experience by offering both the patient and the site an easy-to-schedule e-consent video meeting including a validated digital signature process.

Adherence Risk Management

Early drop-out, an extreme form of patient non-adherence, has been identified as one of the main reasons for extended trial timelines and budgets. However, despite all patient-centric measures taken, recent studies still show that the average early drop-out rate seems to be stagnant at 25%