TY - JOUR
T1 - Enrollment of Participants from Marginalized Racial and Ethnic Groups
T2 - A Comparative Assessment of the STEADY-PD III and SURE-PD3 Trials
AU - Di Luca, Daniel G.
AU - Macklin, Eric A.
AU - Hodgeman, Karen
AU - Lopez, Gisel
AU - Pothier, Lindsay
AU - Callahan, Katherine F.
AU - Lowell, Jill
AU - Chan, James
AU - Videnovic, Aleksandar
AU - Lungu, Codrin
AU - Lang, Anthony E.
AU - Litvan, Irene
AU - Schwarzschild, Michael A.
AU - Simuni, Tatyana
N1 - Funding Information:
The study was funded by the NIH/National Institute of Neurological Disorders and Stroke via grants U01NS090259 and U01NS107009 to Massachusetts General Hospital and U01NS089666 to the University of Rochester, with additional support from the Michael J. Fox Foundation for Parkinson's Research via grants 11942 and 14489. There was also additional support to STEADY-PD III via U01NS080818-01A1 and U01NS080840-01A1 grants.
Publisher Copyright:
© American Academy of Neurology.
PY - 2023/2/18
Y1 - 2023/2/18
N2 - Background and ObjectivesRepresentation of persons from marginalized racial and ethnic groups in Parkinson disease (PD) trials has been low, limiting the generalizability of therapeutic options for individuals with PD. Two large phase 3 randomized clinical trials sponsored by the National Institute of Neurological Disorders and Stroke (NINDS), STEADY-PD III and SURE-PD3, screened participants from overlapping Parkinson Study Group clinical sites under similar eligibility criteria but differed in participation by underrepresented minorities. The goal of this research is to compare recruitment strategies of PD participants belonging to marginalized racial and ethnic groups.MethodsA total of 998 participants with identified race and ethnicity consented to STEADY-PD III and SURE-PD3 from 86 clinical sites. Demographics, clinical trial characteristics, and recruitment strategies were compared. NINDS imposed a minority recruitment mandate on STEADY-PD III but not SURE-PD3.ResultsTen percent of participants who consented to STEADY-PD III self-identified as belonging to marginalized racial and ethnic groups compared to 6.5% in SURE-PD3 (difference = 3.9%, 95% confidence interval [CI] 0.4%-7.5%, p value = 0.034). This difference persisted after screening (10.1% of patients in STEADY-PD III vs 5.4% in SURE-PD 3, difference = 4.7%, 95% CI 0.6%-8.8%, p value = 0.038).DiscussionAlthough both trials targeted similar participants, STEADY-PD III was able to consent and recruit a higher percentage of patients from racial and ethnic marginalized groups. Possible reasons include differential incentives for achieving minority recruitment goals.Trial Registration InformationThis study used data from The Safety, Tolerability, and Efficacy Assessment of Isradipine for Parkinson Disease (STEADY-PD III; NCT02168842) and the Study of Urate Elevation in Parkinson's Disease (SURE-PD3; NCT02642393).
AB - Background and ObjectivesRepresentation of persons from marginalized racial and ethnic groups in Parkinson disease (PD) trials has been low, limiting the generalizability of therapeutic options for individuals with PD. Two large phase 3 randomized clinical trials sponsored by the National Institute of Neurological Disorders and Stroke (NINDS), STEADY-PD III and SURE-PD3, screened participants from overlapping Parkinson Study Group clinical sites under similar eligibility criteria but differed in participation by underrepresented minorities. The goal of this research is to compare recruitment strategies of PD participants belonging to marginalized racial and ethnic groups.MethodsA total of 998 participants with identified race and ethnicity consented to STEADY-PD III and SURE-PD3 from 86 clinical sites. Demographics, clinical trial characteristics, and recruitment strategies were compared. NINDS imposed a minority recruitment mandate on STEADY-PD III but not SURE-PD3.ResultsTen percent of participants who consented to STEADY-PD III self-identified as belonging to marginalized racial and ethnic groups compared to 6.5% in SURE-PD3 (difference = 3.9%, 95% confidence interval [CI] 0.4%-7.5%, p value = 0.034). This difference persisted after screening (10.1% of patients in STEADY-PD III vs 5.4% in SURE-PD 3, difference = 4.7%, 95% CI 0.6%-8.8%, p value = 0.038).DiscussionAlthough both trials targeted similar participants, STEADY-PD III was able to consent and recruit a higher percentage of patients from racial and ethnic marginalized groups. Possible reasons include differential incentives for achieving minority recruitment goals.Trial Registration InformationThis study used data from The Safety, Tolerability, and Efficacy Assessment of Isradipine for Parkinson Disease (STEADY-PD III; NCT02168842) and the Study of Urate Elevation in Parkinson's Disease (SURE-PD3; NCT02642393).
UR - http://www.scopus.com/inward/record.url?scp=85148450439&partnerID=8YFLogxK
U2 - 10.1212/CPJ.0000000000200113
DO - 10.1212/CPJ.0000000000200113
M3 - Article
C2 - 36865634
AN - SCOPUS:85148450439
SN - 2163-0402
VL - 13
JO - Neurology: Clinical Practice
JF - Neurology: Clinical Practice
IS - 1
M1 - e200113
ER -