Randomization is not associated with socio‐economic and demographic factors in a multi‐center clinical trial of children with sickle cell anemia. Issue 9 (22nd April 2014)
- Record Type:
- Journal Article
- Title:
- Randomization is not associated with socio‐economic and demographic factors in a multi‐center clinical trial of children with sickle cell anemia. Issue 9 (22nd April 2014)
- Main Title:
- Randomization is not associated with socio‐economic and demographic factors in a multi‐center clinical trial of children with sickle cell anemia
- Authors:
- Roberts, Dionna O.
Covert, Brittany
Rodeghier, Mark J.
Parmar, Nagina
DeBaun, Michael R.
Thompson, Alexis A.
Liem, Robert I. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25072-sec-0001" sec-type="section"> <title>Background</title> <p>Few studies have investigated factors influencing participation rates for minority children with a chronic disease in clinical trials. The Silent Cerebral Infarct Multi‐Center Clinical (SIT) Trial provides an opportunity to study the impact of demographic and socio‐economic factors on randomization in a clinical trial among Black children. Our primary objective was to characterize the factors associated with successful randomization of children with sickle cell disease (SCD) and silent cerebral infarct (SCI) in the SIT Trial after initial consent.</p> </sec> <sec id="pbc25072-sec-0002" sec-type="section"> <title>Procedure</title> <p>Differences in socio‐economic and demographic variables, family history and disease‐related variables were determined between eligible participants who were successfully randomized and those who were not randomized following initial consent. Head of household educational level and family income were examined separately for US versus non‐US sites.</p> </sec> <sec id="pbc25072-sec-0003" sec-type="section"> <title>Results</title> <p>Of 1, 176 children enrolled in the SIT Trial, 1, 016 (86%) completed screening. Of 208 (20%) children with qualifying SCI on pre‐randomization MRI, 196 (94%) were successfully randomized. There were no differences in socio‐economic, demographic, or<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pbc25072-sec-0001" sec-type="section"> <title>Background</title> <p>Few studies have investigated factors influencing participation rates for minority children with a chronic disease in clinical trials. The Silent Cerebral Infarct Multi‐Center Clinical (SIT) Trial provides an opportunity to study the impact of demographic and socio‐economic factors on randomization in a clinical trial among Black children. Our primary objective was to characterize the factors associated with successful randomization of children with sickle cell disease (SCD) and silent cerebral infarct (SCI) in the SIT Trial after initial consent.</p> </sec> <sec id="pbc25072-sec-0002" sec-type="section"> <title>Procedure</title> <p>Differences in socio‐economic and demographic variables, family history and disease‐related variables were determined between eligible participants who were successfully randomized and those who were not randomized following initial consent. Head of household educational level and family income were examined separately for US versus non‐US sites.</p> </sec> <sec id="pbc25072-sec-0003" sec-type="section"> <title>Results</title> <p>Of 1, 176 children enrolled in the SIT Trial, 1, 016 (86%) completed screening. Of 208 (20%) children with qualifying SCI on pre‐randomization MRI, 196 (94%) were successfully randomized. There were no differences in socio‐economic, demographic, or disease‐related variables between children who were or were not randomized. Participants from non‐US sites were more likely to be randomized (22% vs. 12%, <italic>P</italic> = 0.011); although, randomization by country was associated with neither head of household education nor family income.</p> </sec> <sec id="pbc25072-sec-0004" sec-type="section"> <title>Conclusion</title> <p>In the SIT Trial, acceptance of random allocation was not associated with socio‐economic or demographic factors. Although these factors may represent barriers for some participants, they should not bias investigators caring for children with SCD in their approach to recruitment for clinical trial participation. Pediatr Blood Cancer 2014;61:1529–1535. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 61:Issue 9(2014:Sep.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 61:Issue 9(2014:Sep.)
- Issue Display:
- Volume 61, Issue 9 (2014)
- Year:
- 2014
- Volume:
- 61
- Issue:
- 9
- Issue Sort Value:
- 2014-0061-0009-0000
- Page Start:
- 1529
- Page End:
- 1535
- Publication Date:
- 2014-04-22
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.25072 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2969.xml