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Title: Age and African-American race impact the validity and reliability of the asthma control test in persistent asthmatics.

Authors: Burbank, Allison J; Todoric, Krista; Steele, Pamela; Rosen, Jonathan; Zhou, Haibo; Frye, Marcia; Loughlin, Ceila E; Ivins, Sally; Mills, Katherine; Massey, Lauren Dembnicki; Reeve, Bryce B; Hernandez, Michelle L

Published In Respir Res, (2018 Aug 15)

Abstract: The Asthma Control Test (ACT) is widely used to assess asthma control, yet the validity and reliability of the test have not been specifically evaluated in adolescents or African-Americans. We conducted a prospective psychometric study of the ACT in African-American (AA) and non-African-American (nAA) adolescents with persistent asthma, with emphasis on the clinical utility of the test for medical decision making.Participants completed the ACT and performed spirometry. A physician conducted a guidelines-based assessment of asthma control, blinded to the ACT score. Study procedures were repeated 6-8 weeks later. The ACT-based asthma control assessment was compared to physician assessment.For baseline and follow-up visits, internal consistency, as measured using Cronbach's alpha, was 0.80 and 0.81 in AA teens and 0.80 and 0.83 in nAA teens. Intraclass correlation coefficients were 0.59 and 0.76 in AA and nAA teens, respectively, with stable asthma control over time. Agreement between ACT and physician assessment was moderate in AA teens and fair in nAA teens. An ACT score of ≤19 showed reduced sensitivity for not well controlled asthma in both groups, while a score of ≤21 had the greatest area under the ROC curve. ACT scores were marginally responsive to change in control status.Concerns for the ACT's ability to detect uncontrolled asthma in adolescents emphasizes the need for a more comprehensive evaluation of asthma control in clinical settings. A higher threshold ACT score to define not well controlled asthma may be needed if the ACT is to be used for medical decision making.ClinicalTrials.gov: NCT02671643 , NCT02662413 .

PubMed ID: 30111326 Exiting the NIEHS site

MeSH Terms: No MeSH terms associated with this publication

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