Targeted client communication via mobile devices for improving maternal, neonatal, and child health

Cochrane Database Syst Rev. 2020 Jul 14;8(8):CD013679. doi: 10.1002/14651858.CD013679.

Abstract

Background: The global burden of poor maternal, neonatal, and child health (MNCH) accounts for more than a quarter of healthy years of life lost worldwide. Targeted client communication (TCC) via mobile devices (MD) (TCCMD) may be a useful strategy to improve MNCH.

Objectives: To assess the effects of TCC via MD on health behaviour, service use, health, and well-being for MNCH.

Search methods: In July/August 2017, we searched five databases including The Cochrane Central Register of Controlled Trials, MEDLINE and Embase. We also searched two trial registries. A search update was carried out in July 2019 and potentially relevant studies are awaiting classification.

Selection criteria: We included randomised controlled trials that assessed TCC via MD to improve MNCH behaviour, service use, health, and well-being. Eligible comparators were usual care/no intervention, non-digital TCC, and digital non-targeted client communication.

Data collection and analysis: We used standard methodological procedures recommended by Cochrane, although data extraction and risk of bias assessments were carried out by one person only and cross-checked by a second.

Main results: We included 27 trials (17,463 participants). Trial populations were: pregnant and postpartum women (11 trials conducted in low-, middle- or high-income countries (LMHIC); pregnant and postpartum women living with HIV (three trials carried out in one lower middle-income country); and parents of children under the age of five years (13 trials conducted in LMHIC). Most interventions (18) were delivered via text messages alone, one was delivered through voice calls only, and the rest were delivered through combinations of different communication channels, such as multimedia messages and voice calls. Pregnant and postpartum women TCCMD versus standard care For behaviours, TCCMD may increase exclusive breastfeeding in settings where rates of exclusive breastfeeding are less common (risk ratio (RR) 1.30, 95% confidence intervals (CI) 1.06 to 1.59; low-certainty evidence), but have little or no effect in settings where almost all women breastfeed (low-certainty evidence). For use of health services, TCCMD may increase antenatal appointment attendance (odds ratio (OR) 1.54, 95% CI 0.80 to 2.96; low-certainty evidence); however, the CI encompasses both benefit and harm. The intervention may increase skilled attendants at birth in settings where a lack of skilled attendants at birth is common (though this differed by urban/rural residence), but may make no difference in settings where almost all women already have a skilled attendant at birth (OR 1.00, 95% CI 0.34 to 2.94; low-certainty evidence). There were uncertain effects on maternal and neonatal mortality and morbidity because the certainty of the evidence was assessed as very low. TCCMD versus non-digital TCC (e.g. pamphlets) TCCMD may have little or no effect on exclusive breastfeeding (RR 0.92, 95% CI 0.79 to 1.07; low-certainty evidence). TCCMD may reduce 'any maternal health problem' (RR 0.19, 95% CI 0.04 to 0.79) and 'any newborn health problem' (RR 0.52, 95% CI 0.25 to 1.06) reported up to 10 days postpartum (low-certainty evidence), though the CI for the latter includes benefit and harm. The effect on health service use is unknown due to a lack of studies. TCCMD versus digital non-targeted communication No studies reported behavioural, health, or well-being outcomes for this comparison. For use of health services, there are uncertain effects for the presence of a skilled attendant at birth due to very low-certainty evidence, and the intervention may make little or no difference to attendance for antenatal influenza vaccination (RR 1.05, 95% CI 0.71 to 1.58), though the CI encompasses both benefit and harm (low-certainty evidence). Pregnant and postpartum women living with HIV TCCMD versus standard care For behaviours, TCCMD may make little or no difference to maternal and infant adherence to antiretroviral (ARV) therapy (low-certainty evidence). For health service use, TCC mobile telephone reminders may increase use of antenatal care slightly (mean difference (MD) 1.5, 95% CI -0.36 to 3.36; low-certainty evidence). The effect on the proportion of births occurring in a health facility is uncertain due to very low-certainty evidence. For health and well-being outcomes, there was an uncertain intervention effect on neonatal death or stillbirth, and infant HIV due to very low-certainty evidence. No studies reported on maternal mortality or morbidity. TCCMD versus non-digital TCC The effect is unknown due to lack of studies reporting this comparison. TCCMD versus digital non-targeted communication TCCMD may increase infant ARV/prevention of mother-to-child transmission treatment adherence (RR 1.26, 95% CI 1.07 to 1.48; low-certainty evidence). The effect on other outcomes is unknown due to lack of studies. Parents of children aged less than five years No studies reported on correct treatment, nutritional, or health outcomes. TCCMD versus standard care Based on 10 trials, TCCMD may modestly increase health service use (vaccinations and HIV care) (RR 1.21, 95% CI 1.08 to 1.34; low-certainty evidence); however, the effect estimates varied widely between studies. TCCMD versus non-digital TCC TCCMD may increase attendance for vaccinations (RR 1.13, 95% CI 1.00 to 1.28; low-certainty evidence), and may make little or no difference to oral hygiene practices (low-certainty evidence). TCCMD versus digital non-targeted communication TCCMD may reduce attendance for vaccinations, but the CI encompasses both benefit and harm (RR 0.63, 95% CI 0.33 to 1.20; low-certainty evidence). No trials in any population reported data on unintended consequences.

Authors' conclusions: The effect of TCCMD for most outcomes is uncertain. There may be improvements for some outcomes using targeted communication but these findings were of low certainty. High-quality, adequately powered trials and cost-effectiveness analyses are required to reliably ascertain the effects and relative benefits of TCCMD. Future studies should measure potential unintended consequences, such as partner violence or breaches of confidentiality.

Trial registration: ClinicalTrials.gov NCT02412865 NCT02412956 NCT01610752 NCT03189004 NCT02567006 NCT03024606 NCT02904642 NCT02214849 NCT02781714 NCT02903186 NCT03180138 NCT01894126 NCT01775150 NCT03688217 NCT03612518 NCT03341195 NCT03576157 NCT02371213 NCT03023033 NCT03135288 NCT03332108 NCT03355989 NCT03379467 NCT03402646 NCT03516682 NCT03705455 NCT03797950 NCT03890978 NCT02491177 NCT02662595.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Systematic Review

MeSH terms

  • Breast Feeding / statistics & numerical data
  • Cell Phone*
  • Child Health / standards*
  • Child Health / statistics & numerical data
  • Child, Preschool
  • Communication*
  • Delivery, Obstetric / standards
  • Female
  • HIV Infections / drug therapy
  • Health Behavior
  • Health Services Needs and Demand*
  • Health Status
  • Humans
  • Infant
  • Infant Health / standards*
  • Infant Health / statistics & numerical data
  • Infant, Newborn
  • Maternal Health / standards*
  • Maternal Health / statistics & numerical data
  • Medication Adherence / statistics & numerical data
  • Postpartum Period
  • Pregnancy
  • Prenatal Care / statistics & numerical data
  • Quality Improvement
  • Randomized Controlled Trials as Topic
  • Text Messaging

Associated data

  • ClinicalTrials.gov/NCT02412865
  • ClinicalTrials.gov/NCT02412956
  • ClinicalTrials.gov/NCT01610752
  • ClinicalTrials.gov/NCT03189004
  • ClinicalTrials.gov/NCT02567006
  • ClinicalTrials.gov/NCT03024606
  • ClinicalTrials.gov/NCT02904642
  • ClinicalTrials.gov/NCT02214849
  • ClinicalTrials.gov/NCT02781714
  • ClinicalTrials.gov/NCT02903186
  • ClinicalTrials.gov/NCT03180138
  • ClinicalTrials.gov/NCT01894126
  • ClinicalTrials.gov/NCT01775150
  • ClinicalTrials.gov/NCT03688217
  • ClinicalTrials.gov/NCT03612518
  • ClinicalTrials.gov/NCT03341195
  • ClinicalTrials.gov/NCT03576157
  • ClinicalTrials.gov/NCT02371213
  • ClinicalTrials.gov/NCT03023033
  • ClinicalTrials.gov/NCT03135288
  • ClinicalTrials.gov/NCT03332108
  • ClinicalTrials.gov/NCT03355989
  • ClinicalTrials.gov/NCT03379467
  • ClinicalTrials.gov/NCT03402646
  • ClinicalTrials.gov/NCT03516682
  • ClinicalTrials.gov/NCT03705455
  • ClinicalTrials.gov/NCT03797950
  • ClinicalTrials.gov/NCT03890978
  • ClinicalTrials.gov/NCT02491177
  • ClinicalTrials.gov/NCT02662595