Rationale and design of mDOT-HuA study: a randomized trial to assess the effect of mobile-directly observed therapy on adherence to hydroxyurea in adults with sickle cell anemia in Tanzania

Abel Makubi, Philip Sasi, Mariam Ngaeje, Enrico M Novelli, Bruno P Mmbando, Mark T Gladwin, Julie Makani, Abel Makubi, Philip Sasi, Mariam Ngaeje, Enrico M Novelli, Bruno P Mmbando, Mark T Gladwin, Julie Makani

Abstract

Background: Hydroxyurea (HU) has been demonstrated to be efficacious in reducing complications in individuals with sickle cell anemia (SCA) but poor adherence is a barrier. Directly Observed Therapy (DOT) has been shown to improve adherence in various chronic diseases but there is limited data in adults with SCA.

Methods and design: To examine the effect of mobile-directly observed therapy (mDOT) on adherence to HU (mDOT-HuA) in adults with SCA at Muhimbili National Hospital in Tanzania. The mDOT-HuA study is a single centre, prospective, randomized, open label clinical trial. One-hundred individuals with SCA with haemoglobin SS genotype, aged ≥18 years, living in Dar es Salaam, able and willing to record and submit videos electronically will be included. Participants will be divided into two treatment arms; 50 in the standard monitoring (SM) arm will receive mobile phones and fixed dose HU therapy with standard monitoring; 50 in the mDOT arm will receive mobile phones, fixed dose HU therapy with standard monitoring and a mobile directly observed web based medication adherence monitoring system. The primary outcome is the proportion of participants achieving ≥80 % HU adherence compared between the two arms as assessed through medication possession ratio at the end of 3 months of treatment. REDCap, an open source software application will be used to collect data using clinical research forms. The proportions of adherence in the two arms will be compared by Fisher's exact test. Analysis of outcomes will have performed by both the intention-to treat and per-protocol methods.

Discussion: Should this study become sucessful, it will have the potential for the development of novel strategies for improving HU adherence in SCA.

Trial registration: ClinicalTrials.gov Identifier: NCT02844673 , registered on 25tht July 2016 (retrospectively registered).

Keywords: Adherence; Hydroxyurea; Medication possession ratio; Randomized trial; Sickle cell disease.

Figures

Fig. 1
Fig. 1
Stages of the trial, events and time points. Keys: T time in weeks, − before randomization, FU follow-up, * = participants will be enrolled in 2 months but each of them entering at his/her own time and start screening on the same day
Fig. 2
Fig. 2
Flow chart for study enrollment and randomization. Keys; ALT Alaninie aminotransferase, SM Standard monitoring, MPR Medication possession ratio

References

    1. Makani J, Williams T, Marsh K. Sickle cell disease in Africa: burden and research priorities. Ann Trop Med Parasitol. 2007;101(1):3–14. doi: 10.1179/136485907X154638.
    1. Makani J, et al. Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania. PLoS One. 2011;6(2):14699. doi: 10.1371/journal.pone.0014699.
    1. Creary SE, et al. A pilot study of electronic directly observed therapy to improve hydroxyurea adherence in pediatric patients with sickle-cell disease. Pediatr Blood Cancer. 2014;61(6):1068–1073. doi: 10.1002/pbc.24931.
    1. Candrilli SD, et al. Hydroxyurea adherence and associated outcomes among Medicaid enrollees with sickle cell disease. Am J Hematol. 2011;86(3):273–277. doi: 10.1002/ajh.21968.
    1. Platt OS, et al. Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia. J Clin Invest. 1984;74(2):652–656. doi: 10.1172/JCI111464.
    1. Charache S, et al. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med. 1995;332(20):1317–1322. doi: 10.1056/NEJM199505183322001.
    1. Thornburg CD, et al. Impact of hydroxyurea on clinical events in the BABY HUG trial. Blood. 2012;120(22):4304–4310. doi: 10.1182/blood-2012-03-419879.
    1. Brandow AM, Jirovec DL, Panepinto JA. Hydroxyurea in children with sickle cell disease: practice patterns and barriers to utilization. Blood. 2009;114(22):242.
    1. Kinney TR, et al. Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Blood. 1999;94(5):1550–1554.
    1. Ware RE, et al. Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapy. Blood. 2002;99(1):10–14. doi: 10.1182/blood.V99.1.10.
    1. Grymonpre RE, et al. Pill count, self-report, and pharmacy claims data to measure medication adherence in the elderly. Ann Pharmacother. 1998;32(7–8):749–754. doi: 10.1345/aph.17423.
    1. Thornburg CD, et al. Adherence to hydroxyurea therapy in children with sickle cell anemia. J Pediatr. 2010;156(3):415–419. doi: 10.1016/j.jpeds.2009.09.044.
    1. Thornburg CD, et al. Adherence to study medication and visits: data from the BABY HUG trial. Pediatr Blood Cancer. 2010;54(2):260–264.
    1. Brandow AM, Panepinto JA. Hydroxyurea use in sickle cell disease: the battle with low prescription rates, poor patient compliance and fears of toxicities. Expert Rev Hematol. 2010;3(3):255–260. doi: 10.1586/ehm.10.22.
    1. Moonan PK, et al. Does directly observed therapy (DOT) reduce drug resistant tuberculosis? BMC Public Health. 2011;11(1):1. doi: 10.1186/1471-2458-11-19.
    1. Hart JE, et al. Effect of directly observed therapy for highly active antiretroviral therapy on virologic, immunologic, and adherence outcomes: a meta-analysis and systematic review. J Acquir Immune Defic Syndr. 2010;54(2):167.
    1. Munro SA, et al. Patient adherence to tuberculosis treatment: a systematic review of qualitative research. PLoS Med. 2007;4(7):238. doi: 10.1371/journal.pmed.0040238.
    1. Lanzkron S, et al. Systematic review: hydroxyurea for the treatment of adults with sickle cell disease. Ann Intern Med. 2008;148(12):939–955. doi: 10.7326/0003-4819-148-12-200806170-00221.
    1. Berg KM, et al. Lack of sustained improvement in adherence or viral load following a directly observed antiretroviral therapy intervention. Clin Infect Dis. 2011;53(9):936–943. doi: 10.1093/cid/cir537.
    1. Aker JC, Mbiti IM. Mobile phones and economic development in Africa. J Econ Perspect. 2010;24(3):207–232. doi: 10.1257/jep.24.3.207.
    1. Déglise C, Suggs LS, Odermatt P. SMS for disease control in developing countries: a systematic review of mobile health applications. J Telemed Telecare. 2012;18(5):273–281. doi: 10.1258/jtt.2012.110810.

Source: PubMed

3
구독하다