News in brief: Greenphire's ConneX 'supports trial retention'

By Liza Laws

- Last updated on GMT

© Getty Images
© Getty Images

Related tags Clinical data Clinical data management Clinical trial patient retention

A clinical trial travel solution that can remove administrative burdens for research sites and eliminate logistical and financial barriers for participants has significantly expanded.

Greenphire’s ConneX that can offer personalized concierge services to help with travel to clinical trials announces it has grown in key regions including Japan, central and southern Europe, Scandinavia, and Southeast Asia.

In its research, Greenphire found evidence from the Center for Information and Study on Clinical Research Participation (CISCRP), that clinical trial volunteers listed having to travel to the study clinic as a top disruption yet one that could be overcome.

They also found a recent survey conducted by the Tufts Center for the Study of Drug Development showed the top two ways to enhance patient participation is by implementing patient expense reimbursement (58%) and transportation assistance (55%).

“Delivering a seamless participant experience is critical to study success," said Jim Murphy, CEO of Greenphire.

“Using our ConneX solution, trial sponsors, CROs and sites can do just that – assist participants in navigating the challenges and complexities associated with enrolling and staying enrolled in a study.”

Wanting to support global trial retention, the company says ConneX offers a host of personalized concierge services, including air, train, hotel, car services and rideshare, ambulatory care, and specialty services. This includes travel visa support, with successful applications recently processed for patients traveling from Jordan to Germany and Iraq to the USA.

To learn more visit: https://greenphire.com/participant-travel/.

Related news

Show more

Related products

show more

ODM and CDASH in CRF design

ODM and CDASH in CRF design

Formedix | 10-Mar-2023 | Technical / White Paper

The lesser-known Operational Data Model (ODM) standard is often overlooked as it's not required by any regulators. So, why should you be interested...

4 Warning Signs Your Research Site Is in Trouble

4 Warning Signs Your Research Site Is in Trouble

Elligo Health Research® | 10-Mar-2023 | Insight Guide

You want your clinical research practice to be a success for your business and your patients, but how can you tell if it’s in trouble? Read this article...

How Sponsors Reduce Chaos in Decentralized Trials

How Sponsors Reduce Chaos in Decentralized Trials

Florence Healthcare | 08-Mar-2023 | Insight Guide

89% of research sponsors currently use and expect to continue the use of decentralized technologies and methods, according to our state of the industry...

Standardizing data with NCI controlled terminology

Standardizing data with NCI controlled terminology

Formedix | 13-Feb-2023 | Technical / White Paper

The use of consistent terminology within and between studies is critical to enabling an efficient trial process. CDISC standards such as CDASH, SDTM, SEND...

Related suppliers

Follow us

Products

View more

Webinars