Closing knowledge gaps among parents of children with sickle cell trait

Author:

Beeman Chase M.1,Abrams Mary Ann12,Zajo Kristin3,Stanek Joseph3ORCID,Martinez‐Mendez Alexandra1,Creary Susan E.13ORCID

Affiliation:

1. Center for Child Health Equity and Outcomes Research, Nationwide Children's Hospital The Ohio State University Columbus Ohio USA

2. Primary Care Pediatrics, Department of Pediatrics Nationwide Children's Hospital Columbus Ohio USA

3. Division of Hematology/Oncology/BMT, Department of Pediatrics Nationwide Children's Hospital Columbus Ohio USA

Abstract

AbstractBackgroundDespite needing to be informed about sickle cell trait (SCT) status to make informed reproductive decisions, more than 80% of adults with SCT, including parents of children with SCT who have a high prevalence of SCT, do not know their status.ProcedureThis was a prospective study of parents who received SCT telephone education from the state department of health and then completed SCTaware, a videoconference‐administered SCT education program. The objectives were to evaluate knowledge after telephone education and explore if SCTaware closes knowledge gaps. Participants completed a demographic survey, a health literacy assessment, and reported their SCT status. They completed the Sickle Cell Trait Knowledge Assessment before receiving SCTaware, immediately after, and at follow‐up visits; high knowledge was a score of 75% or higher correct.ResultsSCTaware and the initial surveys were completed by 61 parents; 45 completed the 6‐month surveys. Only 43% of participants had high SCT knowledge after telephone education; 92% achieved high knowledge immediately after, and 84% continued with high knowledge at 6 months. Most parents reported they were aware of their SCT status after telephone education; 12 changed their response after receiving SCTaware.ConclusionsOur findings suggest that over half of parents have low SCT knowledge following telephone education, and many may be unaware of their status. SCTaware closes knowledge gaps, leads to high sustained knowledge, and is a potentially scalable tool. Future studies should refine SCTaware and determine if parents use their knowledge to inform their children and reproductive decisions.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference16 articles.

1. Using qualitative and quantitative strategies to evaluate knowledge and perceptions about sickle cell disease and sickle cell trait;Treadwell MJ;J Natl Med Assoc,2006

2. Acceptability to and Engagement With a Virtual Sickle Cell Trait Education Program (SCTaware): Single-Center Prospective Study

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