Efficacy of text-message reminders on paediatric malaria treatment adherence and their post-treatment return to health facilities in Kenya: a randomized controlled trial
© The Author(s) 2017
Received: 8 November 2016
Accepted: 19 January 2017
Published: 25 January 2017
Short Message Service (SMS) reminders have been suggested as a potential intervention for improving adherence to medications and health facility attendance.
An open-label, randomized, controlled trial to test the efficacy of automated SMS reminders in improving adherence to artemether–lumefantrine (AL) and post-treatment attendance in comparison with standard care was conducted at four health facilities in western Kenya. Children below five years of age with uncomplicated malaria were randomized to intervention (SMS reminders) or control groups. Within each study group they were further randomized to three categories, which determined the timing of home visits to measure adherence to complete AL course and to individual AL doses. A sub-set of caregivers was advised to return to the facility on day 3 and all were advised to return after 28 days. The primary outcomes were adherence to medication and return on day 3. The primary analysis was by intention-to-treat.
Between 9 June, 2014 and 26 February, 2016, 1677 children were enrolled. Of 562 children visited at home on day 3, all AL doses were completed for 97.6% (282/289) of children in the control and 97.8% (267/273) in the intervention group (OR = 1.10; 95% CI = 0.37–3.33; p = 0.860). When correct timing in taking each dose was considered a criteria for adherence, 72.3% (209/289) were adherent in the control and 69.2% (189/273) in the intervention group (OR = 0.82; 95% CI = 0.56–1.19; p = 0.302). Sending SMS reminders significantly increased odds of children returning to the facility on day 3 (81.4 vs 74.0%; OR = 1.55; 95% CI = 1.15–2.08; p = 0.004) and on day 28 (63.4 vs 52.5%; OR = 1.58; 95% CI = 1.30–1.92; p < 0.001).
In this efficacy trial, SMS reminders increased post-treatment return to the health facility, but had no effect on AL adherence which was high in both control and intervention groups. Further effectiveness studies under the real world conditions are needed to determine the optimum role of SMS reminders.
Trial registration ISRCTN39512726
KeywordsSMS Artemether–lumefantrine Adherence Follow-up
The expansion of network coverage and mobile phone penetration in Africa  has offered opportunities to improve health communication and support medical and public health practice . Text messaging or Short Message Service (SMS), the widely used mobile phone function, has recently been deployed in numerous health projects across Africa . Trials across the continent have shown that SMS reminders sent to patients’ mobile phones can improve adherence to antiretroviral therapy [4, 5], immunization coverage , blood pressure control , emotional outcomes after abortion , as well as antenatal , delivery , postpartum , postoperative , and repeat HIV test  attendance. Conversely, in other trials, SMS reminders were not effective in improving adherence to antiretroviral therapy or voluntary male circumcision [14, 15].
Most SMS interventions in Africa have been assessed in the management of chronic diseases and long-term therapy, while their effects on the management of acute diseases, such as malaria, have been less commonly investigated . SMS reminders sent to either health workers or malaria patients and their caregivers have been suggested as a potential intervention [16–18] to improve sub-optimal caregivers’ adherence to artemisinin-based combination therapy (ACT) [19, 20] and poor outpatient attendance rates for follow-up . No previous study has examined the efficacy of SMS reminders to enhance patients’ return to the health facility following malaria treatment. Two trials, showing discrepant results, tested effects of SMS reminders on patients’ adherence to ACT [22, 23].
Non-adherence to anti-malarial medicines and lack of patients’ follow-up compromises malaria case management and favours the emergence of anti-malarial resistance [24, 25]. The latter is becoming increasingly important with the risk of artemisinin resistance spreading from Southeast Asia to sub-Saharan Africa [26–28]. Early warnings of the emergence of resistance may be detected by post-treatment monitoring of the outcomes of ACT treatment [29, 30]. However, such post-treatment monitoring is only possible if patients return to the health facility when requested.
A randomized controlled trial was therefore undertaken in Kenya to assess whether SMS reminders sent to caregivers of children treated with nationally recommended ACT, artemether–lumefantrine (AL), would enhance adherence to AL therapy and would increase the rates of post-treatment return to the health facility following completion of treatment.
The trial was conducted at four public health facilities in Siaya County in western Kenya. Two trial sites are located in Bondo Sub-county (Bondo and Got Agulu Hospitals) and two in Rarieda Sub-county (Ndori Health Centre and Madiany Hospital). Malaria transmission in the study area is high with seasonal peaks in May–July and October–November . AL has been routinely used since 2006 as the first-line treatment for uncomplicated malaria. Reports of children completing AL course ranged from 58–81% [32, 33]. A feasibility study undertaken prior to the trial found that the mobile network coverage in the study area was nearly universal with over 90% of caregivers of children with malaria having access to mobile phones and expressing willingness to receive SMS reminders about drug administration and when to return to the health facility .
All children suspected of malaria were screened by study clinicians at outpatient departments in the study sites and enrolled into the trial if they met all of the following inclusion criteria: age six to 59 months; weight 5 kg and above; history of fever in the previous 24 h or presence of axillary temperature ≥37.5 °C; microscopically confirmed infection of Plasmodium falciparum with parasitaemia between 500 and 200,000/μL; caregiver access to personal or shared mobile phone within household; caregiver ability to open and read SMS either themselves or through another person in the household; and, caregiver provision of written informed consent. The following exclusion criteria applied: presence of clinical danger signs, severe anaemia [haemoglobin (Hb) <5 g/dl] or any other severe malaria criteria; severe malnutrition (weight for height <70%); ongoing prophylaxis with drugs having anti-malarial activity such as cotrimoxazole; reported hypersensitivity to AL; presence of any concurrent illness; and, previous participation in the trial. Thick and thin blood smears were performed by the study microscopists, who counted asexual parasites per 200 white blood cells (WBCs) and calculated parasite density on the estimate of 8000 WBCs/μL. A blood smear was deemed negative only after examining 100 high-power microscopic fields. Hb levels were estimated using HemoCue.
Randomizations and masking
The randomization codes were generated by an offsite statistician and randomization numbers were applied in sequence of recruitment. The trial was open-label. Participants and nurses performing home visits could not be masked. The study personnel at health facilities were necessarily aware of categories for assigning day of home visits, but were blind to the intervention arm.
In both arms children were treated with dispersible AL. The first dose was supervised at the health facility by a study nurse, and repeated if the child vomited within 30 min. The remaining five doses were taken at home. All caregivers received verbal instructions to give the second dose exactly 8 h after the first dose with the subsequent four doses given on the following 2 days at 08.00 in the morning and in the evening at 20.00, and illustrations on the AL blister packs that were taken home were used to support the explanations. Children weighing 5–14 kg were to take single tablet per dose while those weighing 15–24 kg two tablets per dose. The caregivers were advised to administer AL after a meal or with food, to complete all doses even if the child appeared better, and to return to the health facility immediately if the child’s condition worsened.
Content and schedule of SMS reminders
Day of sending
AL dose 2
8 h after first dose
Hello [name of care giver], have you remembered to give your child the [dose number] dose of malaria medicine? If not, please do so. Thank you, [Name of HF]
AL dose 3
AL dose 4
AL dose 5
AL dose 6
Day 3 health facility post-treatment visita
Hello [name of care giver], please remember to bring the child back to hospital [tomorrow on day 2/today on day 3] to confirm clearance of malaria parasites. Thank you, [Name of HF]
Hello [name of care giver] I hope the child is doing well. If not, please bring them back to the hospital as soon as possible. Thank you, [Name of HF]
Day 28 health facility post-treatment visit
Hello [name of care giver], please bring your child back to the hospital [tomorrow on day 27/today on day 28] for day 28 post-treatment as advised by the doctor. Thank you, [Name of HF]
During recruitment, caregivers were informed that they would be visited at home but not informed of the specific day of the visit. They were advised to keep AL blister packs after completing the treatment course. Home visits were undertaken by a study nurse within 24 h of expected completion of the individual doses of interest (doses 2 and 3 in category 1, doses 4 and 5 in category 2, and dose 6 in category 3). During the home visits, adherence to AL was assessed using pill counts and caregivers’ reports to determine the number of pills taken prior to the visit and the timing of each dose. Caregivers were also asked whether they had received text message reminders. Caregivers who returned to the health facility on day 3 (category 1 and 2) were not financially compensated for transport costs as this was considered routine, however those who returned to the facility on day 28 received travel compensation of approximately 2 USD.
Outcomes and definitions
Two primary outcomes were investigated in the trial. The first outcome was the proportion of patients adhering to the complete AL course (doses 2–6) measured in category 3 using the combination of pill count and self-reporting. The definition of correct AL adherence was based on two criteria of which both had to be met: (1) completion of all doses; and, (2) correct timing of all doses. To assess completion of all doses the evidence of empty AL blister pack during the home visit was used. In the absence of blister packs, caregivers’ reports were used. To assess timing, caregivers’ report of administered doses, within ±1 h for dose 2 and ±2 h for doses 3–6, compared to the instructions given at the time of recruitment, was classified as correct. The second primary outcome was the proportion of patients in combined categories 1 and 2 who returned to the health facility on day 3 after expected completion of AL treatment.
Two secondary outcomes were also investigated in the trial. The first secondary outcome was the proportion of patients adhering to the individual AL doses measured within 24 h of expected dose administrations, i.e., for doses 2 and 3 in category 1, doses 4 and 5 in category 2, and for dose 6 in category 3. The adherence definitions for these patient groups followed the criteria of dose completion based on appropriate number of tablets found at the time of the visit and correct timing, using the same time allowances as described for the primary outcome. Finally, the last trial outcome was the proportion of patients across all categories that returned to the health facility on day 28.
Sample size calculation
The sample size estimation was based on the first primary outcome (i.e., adherence to the full course of AL treatment in category 3) . Assuming adherence of 65% in the control group, effect size of 10%, 15% loss to follow-up, 80% power and 0.05 level of significance, the estimated sample size was 400 participants per arm. In addition, 300 participants per arm were included in each of the first and second categories. These sample sizes were estimated to be sufficient to detect an effect size of 10% for an estimated individual AL dose adherence at 75% in the control group, assuming a 10% loss to follow-up and the same power assumptions. Finally, for the measurement of the day 3 return to health facilities, the combined sample size in categories 1 and 2 (600 per arm), had more than 90% power to detect a 10% difference from an estimate for the control group of 45% of patients returning on day 3. Due to slower recruitment than expected and on advice from the Trial Steering Committee, an interim analysis was conducted on the primary adherence outcome in category 3. The interim analysis found ~70% adherence in the control group, higher than the 65% initially estimated, and only 10% rather than 15% loss to follow-up. The sample size was therefore recalculated using other assumptions as above and the recruitment was terminated when 645 patients in category 3 and 1677 in total were enrolled.
The primary analytic approach was intention-to-treat (ITT) including all randomized patients with available outcome data. The secondary analytic approach was per-protocol (PP) where adherence analyses excluded patients who were inadvertently recruited without meeting enrolment criteria and those who did not receive SMS reminders in the intervention group. SMS exposure was classified on the basis of a caregiver’s report regarding delivery of any SMS reminder.
To estimate effects of the intervention on outcomes, mixed effects logistic regression models, with intervention arm as an independent variable adjusted for clustering by site, was used. The effect was expressed as an odds ratio (OR) with corresponding 95% confidence interval and p value. Participants’ characteristics were tabulated by randomization group. To further assess potential confounders, multivariable regression was performed by examining each potential confounder as an independent variable with randomization group and retaining any of the covariates, which changed the unadjusted OR of randomization group by more than 5%.
All trial data were double entered, verified and cleaned in Access 2013 (Microsoft Corporation, Seattle, WA), and thereafter analysed in Stata version 12 (StataCorp, College Station, TX).
Enrolment and patient characteristics
The characteristics of the study subjects by arm and category
Control N = 254
Intervention N = 259
Control N = 262
Intervention N = 257
Control N = 333
Intervention N = 312
Control N = 849
Intervention N = 828
Temperature ≥37.5 °C
Parasite density >10,000/µl
Relationship to the child
No formal education
Secondary and above
Phone ownership status
Adherence to complete AL course
Effects of the intervention on AL adherence measured the day after expected completion of the full 3-day course—ITT analysis in category 3
N = 289
N = 273
N = 562
OR (95% CI)
All AL doses completed
All doses timely completed
Adherence to individual AL doses
Effects of the intervention on adherence to individual AL doses measured within 24 h of expected completion of the specific dose—ITT analysis by category
OR (95% CI)
N = 237
N = 241
n = 478
N = 226
N = 239
N = 465
N = 289
N = 273
N = 562
Patients’ return to health facility
Effects of the intervention on patients return to the health facility for post-treatment review
OR (95% CI)
Day 3 return
N = 516
N = 516
N = 1032
(Patients from category 1 and 2)
Day 28 return
N = 849
N = 828
N = 1677
(Patients from all categories)
Adjustment for covariates
No covariate met the 5% inclusion criteria described above for either outcome of interest (Additional files 3 and 4) and therefore only unadjusted effects of the intervention are presented, as above. Furthermore, no covariate showed statistically significant associations with outcome at p value of <0.10 on ITT or on PP analysis (Additional files 3 and 4).
This randomized controlled trial in western Kenya showed that SMS reminders significantly increased the rates of return to the health facility following anti-malarial treatment but did not have any effect on adherence to AL medications. The results of this efficacy trial comparing an SMS intervention to optimum clinical practices have several important implications.
Nearly all children completed all AL doses in this trial, which indicates substantially higher adherence than previously observed in evaluations conducted under the routine conditions in the same area [32, 33], in other parts of Kenya , and across Africa [40–45]. The high availability of AL blister packs during home visits and the evidence of empty packs provided confidence of high completion rates. Timely completion of all AL doses was lower (71%), but still substantially higher than reported in many previous studies [23, 40–42]. Adherence results for individual doses measured by home visits conducted closer to the expected time of administration were similar with measurements three days after the treatment. This suggests that self-reporting was unlikely to have introduced recall bias. While non-completion of AL doses compromises treatment outcome and contributes to the development of resistance [25, 46, 47] it is unclear how strictly dose intervals must be adhered to in order to avoid adverse consequences and this trial was not designed to examine this.
Two other previous effectiveness trials tested effects of innovative SMS reminders on patients’ adherence to anti-malarials and these showed discordant results, but lower overall adherence [22, 23]. Due to methodological differences where different modalities of SMS interventions were used in different settings, comparisons between studies are problematic. Under the trial conditions reported here, SMS reminders were unnecessary as adherence levels were already high. It is possible that the excluded patients from the trial were those in whom poor adherence was most likely. This can only be a partial explanation for high adherence rates, since relatively few caregivers were excluded simply because they declined to take part or lacked access to SMS reminders (most exclusions were for children without malaria).
A recent review of anti-malarial adherence studies suggests that interactions between research teams or medical staff and patients is likely to influence adherence levels . Specifically, the conduct of consultations by research staff, parasitological confirmation, consenting of patients prior to the treatment, awareness of participants about home visits, dispenser’s observation of the swallowing of the first dose, may all have contributed to higher adherence levels in this trial. The importance of optimum clinical practices, including appropriate drug dispensing and counselling according to standard guidelines, either provided under the trial or routine conditions, seems to be a factor for adherence . Under ‘real world’ conditions SMS reminders may lead to improved adherence to anti-malarial medicines . However it can be argued that ‘real world’ conditions can be altered by the implementation of policy. For instance, healthcare providers in routine settings could provide explanations and demonstrate the illustrated instructions on blister packs as done in this trial. The investment required for SMS reminder systems should be compared against investment in the basic essentials and interventions to improve provider adherence to national treatment guidelines.
In contrast to the findings on adherence, SMS reminders increased the rates of patients returning to health facilities for routine follow-up. Increasing the day 3 return from 74 to 81% and the day 28 return from 53 to 63% is a relatively modest but still significant impact on behaviour. Two trials in Kenya have shown similar effects of SMS on postpartum  and postoperative  attendance, as well as a larger 18% effect on attendance for follow-up HIV testing . Post-treatment attendances among patients not receiving SMS reminders were significantly higher than the range 12–41% observed in Kenyan appointment trials, as well as higher than the 44% of sick children returning to health facility following outpatient counselling in Sudan . In the Kenyan trial reported in this manuscript, day 28 returns are likely to have been positively influenced by financial transport compensations and day 3 returns are likely to have been influenced by home visits. Nevertheless, the SMS reminder was seen to be significant in improving returns at both day 3 and day 28 despite this background. The costs and benefits of improved day 3 post-treatment returns among children receiving SMS reminders should be considered for routine use, particularly given the importance of pragmatic, artemisinin resistance monitoring [29, 30].
When optimum care under the trial conditions is provided, text-message reminders can increase a child’s return to the health facility following anti-malarial treatment, without an additional effect on already high levels of AL adherence that occur under trial conditions. Further effectiveness studies under varying real world conditions in different settings are needed to determine the optimum role of text-message reminders in improving patients’ adherence to anti-malarial medicines.
AOT, RWS and DZ originated the idea and were involved in the design of the trial. AOT, AO, SG, CJ, and JM were involved in the development of the standard operating procedures, data collection tools and structure of the database. AOT, JM and BA cleaned and analysed data. PB provided input in trial management and revised the manuscript. AOT and DZ drafted the manuscript. All authors read and approved the final manuscript.
This research was supported by the MRC/DfID/Wellcome Trust Joint Global Health Trial scheme (Grant #MR/K007351/1 to AOT). This UK funded award is part of the European and Developing Countries Clinical Trials Partnership (EDCTP2) programme supported by the European Union. RWS is supported by the Wellcome Trust as Principal Research Fellow (# 079080 & # 103602). We would like to thank the members of the Trial Steering Committee namely: Professor Umberto D’Alessandro (chairperson), Dr. Alex Rowe (member), Dr. Modest Mulenga (member) and Ms Jennifer O’ Callaghan (funder’s representative). We are grateful to all caregivers of children who participated in the study. This paper is submitted with the permission of the Director of KEMRI.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets analysed during the study are available on reasonable request.
Ethics approval and consent to participate
The protocol was approved by the Kenya Medical Research Institute (KEMRI) ethical review committee (SSC Protocol No 2554) and the University of Oxford ethical review board (OXTREC Number 1011-13). Written informed consent was obtained from caregivers of all study participants. The trial was registered at the ISRCTN registry (ISRCTN39512726).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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