Last Updated: 27/11/2025
Efficacy of mobile phone short message service (SMS) on malaria treatment adherence and post-treatment review
Objectives
This project grant aims to investigate the efficacy of mobile phone SMS text messaging in improving malaria treatment adherence and promoting post-treatment review, in an endeavor to provide novel approaches for the mitigation, early warning, and early detection of emerging drug resistance in Africa.
A “proof of concept” multi-centre randomised controlled clinical trial will be conducted to assess the efficacy of mobile phone short message service (SMS) on treatment adherence and day 3 and 28 post-treatment review. The principal research questions are two-fold:
- First, can innovative ways, such as SMS text messaging, improve patient adherence to malaria treatment?
- Second, can SMS text messaging bring back more patients for post-treatment review? The latter will enable the assessment of the operational feasibility of collecting, in routine settings, the clinical and parasitological cure rates at days 3 and 28.
KEMRI Wellcome Trust Research Programme, Kenya
University of Oxford, United Kingdom
Artemisinin resistant falciparum malaria has emerged in south East Asia (SEA), an ominous repetition of the spread of chloroquine and later of sulfadoxine-pyrimethamine resistance, several decades ago. Recent evidence suggests artemisinin resistance foci in Western Cambodia, Western Thailand, and Burma. This poses a major global public health threat, with the greatest potential effects in sub-Saharan Africa where the disease burden is greatest and systems for resistance monitoring and containment are weakest. A public health disaster is imminent unless mitigation and early warning/early detection measures are urgently set up. The mechanisms underlying artemisinin resistance are currently not fully understood. The main phenotype associated with resistance is a substantial delay in parasite clearance, so far observed in SEA but not yet unequivocally confirmed in Africa. Poor patient adherence to treatment and drug misuse are of the drivers of antimalarial resistance. Poor adherence decreases cure rates because parasites are exposed to sub-therapeutic drug concentrations, favouring the emergence of resistance. Recent evidence suggests that the traditional approaches (provider counselling and caregiver aids) for improving patient adherence in routine settings are suboptimal. Urgent research is thus needed to investigate innovative approaches to address this problem. Secondly, the most widely used methodological approaches for adherence measurement, conducted after the completion of a full dose of artemether-lumefantrine (AL), the most widely used artemisinin combination therapy (ACT) in rural Africa, have inherent recall bias and do not capture the timing of dosing, which is critical for AL. Better patient adherence to malaria treatment is likely to improve health outcomes and mitigate the emergence of falciparum drug resistance in Africa. Detecting emerging artemisinin resistance in Africa is likely to require wide coverage surveillance, beyond the traditional sentinel surveillance. Better surveillance through routine health information systems (HIS), of the proportion of patients who remain parasite positive at day 3 and the proportion requiring rescue therapy during one month after ACT treatment, could offer new opportunities to track highly sensitive and pragmatic markers for emerging ACT resistance. However, malaria post-treatment review to capture these surrogate markers, outside the context of a clinical trial, is rare in most of rural Africa, and innovative ways of promoting this practice are urgently needed. Mobile phone communication has been suggested as a method to improve the delivery of health services in Africa, and its role has been investigated in improving health information reporting, provider performance, drug and diagnostic stock management, and patient adherence to treatment for chronic diseases such as HIV/AIDs. However, the efficacy of mobile phone text messaging in improving patients’ adherence and promoting posttreatment review for acute diseases such as malaria has not been investigated.
ISRCTN39512726
- Primary study design: Interventional
- Study design: Randomized controlled clinical trial
- Secondary study design: Randomised controlled trial
Mar 2013 — Mar 2017
$1.98M


