ALS & PARTICIPATION IN CLINICAL RESEARCH
The Les Turner ALS Foundation, in partnership with NEALS, is proud to present a comprehensive guide aimed at demystifying clinical research for ALS.
A Guide for People Living with ALS
This ALS & Participation in Clinical Research guide offers an overview of clinical trials, highlighting the phases, potential benefits, and significant role that people living with ALS and their families can play in advancing research and treatment options.
The guide also provides essential tips on evaluating participation in clinical research, ensuring that patients, caregivers, and family members are fully informed and supported. Developed in collaboration with people living with ALS, caregivers, advocates, and NEALS members, it adheres to best practices in health literacy. This is a crucial tool for anyone in the ALS community looking to engage with or understand more about clinical research.