Social- and Health Care-Related Influences on Multiple Sclerosis Outcomes

This study investigates the impact of social and health care factors on disability, quality of life, mood, and other outcomes in people with MS from diverse backgrounds. The survey is currently available in English and will soon be available in Spanish. La encuesta está actualmente disponible en inglés y pronto estará disponible en español. This study is fully remote and does not require any in-person visits.

Actively Recruiting
Yes
Duration

Participation lasts 45-60 minutes.

Inclusion Criteria
  • 18+ years of age
  • Currently live in the United States
  • Neurologist or doctor confirmed diagnosis of MS
  • Able to speak, write, and read fluently in English and/or Spanish
  • Access to a computer, tablet, or smartphone with internet
  • Identify as:
  1. Hispanic/Latino/a
  2. Black/African American
  3. Asian
  4. Indigenous / Native American
  5. Native Alaskan
  6. Native Hawaiian or other Pacific Islander
  7. Biracial or Multi-racial
  8. Other diverse group not listed here

La versión en español de la encuesta en línea estará disponible en unas semanas. Si está interesado en participar, comuníquese con nosotros para obtener más información y ponerse en una lista de espera.

Compensation

Amazon Gift Card

IRB Number:

R-1216-23

Research Center
Rocco Ortenzio Neuroimaging Center
Contact
[email protected]