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How to Give Your Clinical Trial Participants More Control, Convenience & Comfort
Inclusivity, Engagement Leslie Yates Inclusivity, Engagement Leslie Yates

How to Give Your Clinical Trial Participants More Control, Convenience & Comfort

Some estimates indicate 80% of trials are delayed due to participant retention challenges. However, sponsors and CRO’s can curb this attrition by focusing their trials on patient comfort, convenience, and by ensuring they feel in control of their participation. Adopting a truly patient-centered study design means acknowledging that every patient comes in with differing needs surrounding these three tenets and addressing them throughout trial design and execution.

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Make the most of data collection with these 4 simple steps
Insights Leslie Yates Insights Leslie Yates

Make the most of data collection with these 4 simple steps

Questions have always existed around data from patients, and it's largely due to the ongoing challenges that are faced that make it difficult to detect noise such as recall bias, observer-expectancy effect, and response bias. The capability to overcome these challenges within the industry is an innovative process of combining these data collection methods into one cohesive offering.

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Scaling your global hybrid-decentralized study
DCTs, Insights Leslie Yates DCTs, Insights Leslie Yates

Scaling your global hybrid-decentralized study

Whether you're planning your next clinical trial or looking to gradually expand your current hybrid-decentralized trial there are numerous decentralized clinical trial approaches and steps you can put in place for your projects, such as virtual visits within protocol, schedule of events (SoE), and ICF’s that can make scaling your study become a turn-key process.

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