Recruitment of infants with sickle cell anemia to a Phase III trial: data from the BABY HUG study

Lynn Wynn, Scott Miller, Lane Faughnan, Zhaoyu Luo, Ellen Debenham, Lea Adix, Billie Fish, Tally Hustace, Tracy Kelly, Marylou Macdermott, Joan Marasciulo, Brenda Martin, Jennifer McDuffie, Mary Murphy, Betsy Rackoff, Caroline Reed, Phillip Seaman, Glenda Thomas, Winfred Wang, Lynn Wynn, Scott Miller, Lane Faughnan, Zhaoyu Luo, Ellen Debenham, Lea Adix, Billie Fish, Tally Hustace, Tracy Kelly, Marylou Macdermott, Joan Marasciulo, Brenda Martin, Jennifer McDuffie, Mary Murphy, Betsy Rackoff, Caroline Reed, Phillip Seaman, Glenda Thomas, Winfred Wang

Abstract

Background: Protocol-eligible subjects may not be candidates for research participation or may decline. To determine factors that affected accrual, we evaluated enrollment in BABY HUG, a multi-center, randomized, placebo-controlled Phase III trial of hydroxyurea (HU) in infants with sickle cell anemia.

Methods: An anonymized registry of potential subjects served as the primary source of data. Study coordinators considered all infants less than age 18 months with a hemoglobin FS diagnosis on newborn screening. Data included the number of potentially eligible subjects, whether parents were approached, and reasons for participating or declining.

Results: Of 1106 potential participants, 28% were not approached for reasons such as prior poor adherence to clinical care. Interested families expressed willingness to contribute to medical knowledge (51%), hope of being randomized to receive hydroxyurea (51%), and desire for closer clinical care (51%) as reasons for participating. Disease severity or the perception that their child was ill had less impact on willingness to participate (16%). Parents who declined cited fear of research (19%), transportation problems (14%), and the demanding nature of the study (25%). Ultimately, 234 (21%) gave informed consent, with little variability of acceptance rates among sites. Importantly, the number of subjects enrolled correlated with the number of families that were approached. Sites that excluded patients based on clinical/psychosocial biases were not more successful in recruiting than those who approached all eligible subjects.

Conclusion: Large, demanding clinical trials require an adequate pool of potential participants. Approaching all potentially eligible patients without predetermined biases enhances success in recruitment.

Copyright © 2010 Elsevier Inc. All rights reserved.

Figures

Figure 1
Figure 1
Flow Chart of BABY HUG Recruitment
Figure 2
Figure 2
Patients Available, Approached and Consented across 14 Sites
Figure 3
Figure 3
Ratios of Consented/Approached and Approached/Available Note: The green diamond at the bottom is an outlier and it is not included in our regression model.

Source: PubMed

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