Excluding People With Disabilities From Clinical Research: Eligibility Criteria Lack Clarity And Justification

Publication

Published on: October 3, 2022

Published inHealth Affairs

Abstract
The exclusion of people with disabilities from clinical research without appropriate justification is discriminatory, is counter to federal regulations and research guidelines, and limits study generalizability. This matter is understudied, and data on the disability status of trial participants are rarely collected or reported. We analyzed ninety-seven recent interventional protocols in four therapeutic areas registered on ClinicalTrials.gov. Eighty-five percent of protocols allowed broad investigator discretion to determine eligibility, whereas only 18 percent explicitly permitted people with disabilities to use forms of support (such as supported decision making or assistive devices) to facilitate study participation. Eligibility criteria affecting people with disabilities included exclusions for psychiatric (68 percent), substance use (62 percent), HIV or hepatitis (53 percent), cognitive or intellectual (42 percent), visual (34 percent), hearing (10 percent), mobility (9 percent), long-term care (6 percent), and speech and communication (3 percent) disability-related domains. Documented justification was provided for only 24 percent of these exclusions. We recommend greater scrutiny of study eligibility criteria, scientific or ethical justification of exclusions, and accessible study design.

Diversity, Inclusion, and Equity in Clinical Research: Integrating Considerations for Diversity, Equity, and Inclusion (DEI) into a Recruitment Strategy Document

Tools

Developed on: October 2022

Developed by: MRCT Center Diversity Workgroup

Related Resources

Procedural & Logistical Checklist

An IRB Resource for Participants: Costs and Payments

An IRB Resource for Investigators and Research Teams– Practical Points to Consider: Payment to Research Participants

An IRB Resource for Investigators and Research Teams: Including the Community Voice in Clinical Research

Incorporating DEI into Clinical Research Protocol Templates

Diversity & Inclusion Overlay: TransCelerate’s Common Protocol Template

Diversity & Inclusion Overlay: NIH-FDA Phase 2 and 3 IND/IDE Clinical Trial Protocol Template

See related Resources, maintained on our project specific website:
Diversity, Inclusion, and Equity in Clinical Research website

IRB Resources

Pediatric Research Informational Materials

Developed: August 2022

Developed by: MRCT Center Pediatrics Workgroup

The MRCT Center worked with high school and college students to develop educational brochures on various research topics. These brochures were reviewed by international youth advisory networks and are written for 12- to 17-year-olds.