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Recruitment of pre-dementia participants: main enrollment barriers in a longitudinal amyloid-PET study.

Authors :
Bader, Ilse
Bader, Ilona
Lopes Alves, Isadora
Vállez García, David
Vellas, Bruno
Dubois, Bruno
Boada, Mercè
Marquié, Marta
Altomare, Daniele
Scheltens, Philip
Vandenberghe, Rik
Hanseeuw, Bernard
Schöll, Michael
Frisoni, Giovanni B.
Jessen, Frank
Nordberg, Agneta
Kivipelto, Miia
Ritchie, Craig W.
Grau-Rivera, Oriol
Molinuevo, José Luis
Source :
Alzheimer's Research & Therapy. 11/2/2023, Vol. 15 Issue 1, p1-14. 14p.
Publication Year :
2023

Abstract

Background: The mismatch between the limited availability versus the high demand of participants who are in the pre-dementia phase of Alzheimer's disease (AD) is a bottleneck for clinical studies in AD. Nevertheless, potential enrollment barriers in the pre-dementia population are relatively under-reported. In a large European longitudinal biomarker study (the AMYPAD-PNHS), we investigated main enrollment barriers in individuals with no or mild symptoms recruited from research and clinical parent cohorts (PCs) of ongoing observational studies. Methods: Logistic regression was used to predict study refusal based on sex, age, education, global cognition (MMSE), family history of dementia, and number of prior study visits. Study refusal rates and categorized enrollment barriers were compared between PCs using chi-squared tests. Results: 535/1856 (28.8%) of the participants recruited from ongoing studies declined participation in the AMYPAD-PNHS. Only for participants recruited from clinical PCs (n = 243), a higher MMSE-score (β = − 0.22, OR = 0.80, p <.05), more prior study visits (β = − 0.93, OR = 0.40, p <.001), and positive family history of dementia (β = 2.08, OR = 8.02, p <.01) resulted in lower odds on study refusal. General study burden was the main enrollment barrier (36.1%), followed by amyloid-PET related burden (PCresearch = 27.4%, PCclinical = 9.0%, X2 = 10.56, p =.001), and loss of research interest (PCclinical = 46.3%, PCresearch = 16.5%, X2 = 32.34, p <.001). Conclusions: The enrollment rate for the AMYPAD-PNHS was relatively high, suggesting an advantage of recruitment via ongoing studies. In this observational cohort, study burden reduction and tailored strategies may potentially improve participant enrollment into trial readiness cohorts such as for phase-3 early anti-amyloid intervention trials. The AMYPAD-PNHS (EudraCT: 2018–002277-22) was approved by the ethical review board of the VU Medical Center (VUmc) as the Sponsor site and in every affiliated site. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17589193
Volume :
15
Issue :
1
Database :
Academic Search Index
Journal :
Alzheimer's Research & Therapy
Publication Type :
Academic Journal
Accession number :
173429765
Full Text :
https://doi.org/10.1186/s13195-023-01332-4