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HABIT, a Randomized Feasibility Trial to Increase Hydroxyurea Adherence, Suggests Improved Health-Related Quality of Life in Youths with Sickle Cell Disease.
Smaldone, Arlene; Findley, Sally; Manwani, Deepa; Jia, Haomiao; Green, Nancy S.
Afiliación
  • Smaldone A; Columbia University School of Nursing, New York, NY; College of Dental Medicine, Columbia University Medical Center, New York, NY. Electronic address: ams130@columbia.edu.
  • Findley S; Mailman School of Public Health, Columbia University, New York, NY.
  • Manwani D; Department of Pediatrics, Albert Einstein College of Medicine, New York, NY.
  • Jia H; Columbia University School of Nursing, New York, NY; Mailman School of Public Health, Columbia University, New York, NY.
  • Green NS; Department of Pediatrics, Columbia University Medical Center, New York, NY.
J Pediatr ; 197: 177-185.e2, 2018 06.
Article en En | MEDLINE | ID: mdl-29571930
ABSTRACT

OBJECTIVES:

To examine the effect of a community health worker (CHW) intervention, augmented by tailored text messages, on adherence to hydroxyurea therapy in youths with sickle cell disease, as well as on generic and disease-specific health-related quality of life (HrQL) and youth-parent self-management responsibility concordance. STUDY

DESIGN:

We conducted a 2-site randomized controlled feasibility study (Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment [HABIT]) with 21 intervention allocation. Youths and parents participated as dyads. Intervention dyads received CHW visits and text message reminders. Data were analyzed using descriptive statistics, the Wilcoxon signed-rank test, and growth models adjusting for group assignment, time, and multiple comparisons. Changes in outcomes from 0 to 6 months were compared with their respective minimal clinically important differences.

RESULTS:

A total of 28 dyads (mean age of youths, 14.3 ± 2.6 years; 50% Hispanic) participated (18 in the intervention group, 10 in the control group), with 10.7% attrition. Accounting for group assignment, time, and multiple comparisons, at 6 months intervention youths reported improved generic HrQL total score (9.8 points; 95% CI, 0.4-19.2) and Emotions subscale score (15.0 points; 95% CI, 1.6-28.4); improved disease-specific subscale scores for Worry I (30.0 points; 95% CI, 8.5-51.5), Emotions (37.0 points, 95% CI, 9.4-64.5), and Communication I (17.8 points; 95% CI, 0.5-35.1); and 3-month dyad self-management responsibility concordance (3.5 points; 95% CI, -0.2 to 7.1). There were no differences in parent proxy-reported HrQL measures at 6 months.

CONCLUSIONS:

These findings add to research examining effects of behavioral interventions on HrQL outcomes in youths with sickle cell disease. TRIAL REGISTRATION ClinicalTrials.gov NCT02029742.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Terapia Conductista / Agentes Comunitarios de Salud / Cumplimiento de la Medicación / Hidroxiurea / Anemia de Células Falciformes Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: J Pediatr Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Terapia Conductista / Agentes Comunitarios de Salud / Cumplimiento de la Medicación / Hidroxiurea / Anemia de Células Falciformes Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: J Pediatr Año: 2018 Tipo del documento: Article