Why Diversity In Health Research Is Good Science And Good Business - Vibrent
Content by Vibrent’s CEO | February 28, 2022

Why Diversity In Health Research Is Good Science And Good Business

By Praduman "PJ" Jain, Praduman "PJ" Jain

Recruiting and retaining participants for clinical research — let alone those that represent diverse populations — has historically been a major challenge that negatively impacts all of us. Just the cost of losing and replacing participants in research trials can rack up thousands to millions of dollars per trial. In 2019, the average participant dropout rate for late-stage research trials was around 19.1% globally according to recent research results, up from 15.3% in 2012.

But the cost of enrolling and maintaining diverse research participants in medical research cuts deeper than wasted funds and often disproportionally excludes the most vulnerable, unrepresented members of our society. In 2014, some 86% of participants in clinical trials listed with the U.S. Food and Drug Administration were white. The results of a 2021 study show that white individuals accounted for 77.9% of participants in vaccine clinical trials run in the U.S. between 2011 and 2020.

Read more at Forbes.

More to read

Paper Newly Published in JMIR Demonstrates the Efficacy of Digital Platforms to Increase Engagement with Diverse Populations in Health Research
Scientific Publication

Paper Newly Published in JMIR Demonstrates the Efficacy of Digital Platforms to Increase Engagement with Diverse Populations in Health Research

FAIRFAX, Va.--25 Jan., 2025--A pioneering study titled "Building a Digital Health Research Platform to Enable Recruitment, Enrollment, Data Collection, and…

Content by Vibrent’s CEO

Technology considerations to promote inclusion, equity and diversity in clinical research

Underrepresented groups traditionally were thought to have limited access to technology. But internet access is on the rise and researchers…

Blog

eConsent Best Practices 

Electronic informed consent, also known as electronic consent or eConsent for short, is a digital way of capturing consent to…

Blog

Community Engagement Paves the Way for Reducing Health Disparities in Cancer Research: An Interview with Dr. Katherine Tossas 

Dr. Katherine Tossas How do you approach underserved communities for collaboration in your health research? With humility and flexibility, says…

Blog

eConsent Done Right: A Powerful Tool to Build Trust and Diversity in Research 

Researchers use a variety of tools and techniques to reach out and recruit diverse participants to their studies. But the…

Blog

What Researchers Need to Know for the Week of April 4, 2022

The news cycle last week was full of government updates, but the area of genomics was particularly active.   The…

Blog

Are Your Digital Tools an Unintended Barrier to Diversity in Research? How to Bridge the Technology Gap for Research Participants

Since the start of the pandemic, researchers have faced additional challenges in participant recruitment and engagement. Safety and exposure concerns…

Blog

To Create a Diverse Research Participant Population, Start with These Strategies

The past two years have revealed the ugly truth about diversity in research: it’s not been a priority. But with…

Blog

To Recruit Diverse Research Participants, Get Out of the Clinic and into Your Community

Most research studies are performed in clinic-based academic medical center facilities. Centralizing resources – technology, laboratory facilities, and skilled clinical…

Blog

What Researchers Need to Know for the Week of March 28, 2022

In health research, it’s hard to keep up. There are new discoveries made, new projects begun, and new innovations announced…

SCROLL