Targeted client communication via mobile devices for improving sexual and reproductive health

Cochrane Database Syst Rev. 2020 Jul 14;8(8):CD013680. doi: 10.1002/14651858.CD013680.

Abstract

Background: The burden of poor sexual and reproductive health (SRH) worldwide is substantial, disproportionately affecting those living in low- and middle-income countries. Targeted client communication (TCC) delivered via mobile devices (MD) (TCCMD) may improve the health behaviours and service use important for sexual and reproductive health.

Objectives: To assess the effects of TCC via MD on adolescents' knowledge, and on adolescents' and adults' sexual and reproductive health behaviour, health service use, and health and well-being.

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 of TCC via MD to improve sexual and reproductive health behaviour, health service use, and health and well-being. Eligible comparators were standard care or no intervention, non-digital TCC, and digital non-targeted 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. We have presented results separately for adult and adolescent populations, and for each comparison.

Main results: We included 40 trials (27 among adult populations and 13 among adolescent populations) with a total of 26,854 participants. All but one of the trials among adolescent populations were conducted in high-income countries. Trials among adult populations were conducted in a range of high- to low-income countries. Among adolescents, nine interventions were delivered solely through text messages; four interventions tested text messages in combination with another communication channel, such as emails, multimedia messaging, or voice calls; and one intervention used voice calls alone. Among adults, 20 interventions were delivered through text messages; two through a combination of text messages and voice calls; and the rest were delivered through other channels such as voice calls, multimedia messaging, interactive voice response, and instant messaging services. Adolescent populations TCCMD versus standard care TCCMD may increase sexual health knowledge (risk ratio (RR) 1.45, 95% confidence interval (CI) 1.23 to 1.71; low-certainty evidence). TCCMD may modestly increase contraception use (RR 1.19, 95% CI 1.05 to 1.35; low-certainty evidence). The effects on condom use, antiretroviral therapy (ART) adherence, and health service use are uncertain due to very low-certainty evidence. The effects on abortion and STI rates are unknown due to lack of studies. TCCMD versus non-digital TCC (e.g. pamphlets) The effects of TCCMD on behaviour (contraception use, condom use, ART adherence), service use, health and wellbeing (abortion and STI rates) are unknown due to lack of studies for this comparison. TCCMD versus digital non-targeted communication The effects on sexual health knowledge, condom and contraceptive use are uncertain due to very low-certainty evidence. Interventions may increase health service use (attendance for STI/HIV testing, RR 1.61, 95% CI 1.08 to 2.40; low-certainty evidence). The intervention may be beneficial for reducing STI rates (RR 0.61, 95% CI 0.28 to 1.33; low-certainty evidence), but the confidence interval encompasses both benefit and harm. The effects on abortion rates and on ART adherence are unknown due to lack of studies. We are uncertain whether TCCMD results in unintended consequences due to lack of evidence. Adult populations TCCMD versus standard care For health behaviours, TCCMD may modestly increase contraception use at 12 months (RR 1.17, 95% CI 0.92 to 1.48) and may reduce repeat abortion (RR 0.68 95% CI 0.28 to 1.66), though the confidence interval encompasses benefit and harm (low-certainty evidence). The effect on condom use is uncertain. No study measured the impact of this intervention on STI rates. TCCMD may modestly increase ART adherence (RR 1.13, 95% CI 0.97 to 1.32, low-certainty evidence, and standardised mean difference 0.44, 95% CI -0.14 to 1.02, low-certainty evidence). TCCMD may modestly increase health service utilisation (RR 1.17, 95% CI 1.04 to 1.31; low-certainty evidence), but there was substantial heterogeneity (I2 = 85%), with mixed results according to type of service utilisation (i.e. attendance for STI testing; HIV treatment; voluntary male medical circumcision (VMMC); VMMC post-operative visit; post-abortion care). For health and well-being outcomes, there may be little or no effect on CD4 count (mean difference 13.99, 95% CI -8.65 to 36.63; low-certainty evidence) and a slight reduction in virological failure (RR 0.86, 95% CI 0.73 to 1.01; low-certainty evidence). TCCMD versus non-digital TCC No studies reported STI rates, condom use, ART adherence, abortion rates, or contraceptive use as outcomes for this comparison. TCCMD may modestly increase in service attendance overall (RR: 1.12, 95% CI 0.92-1.35, low certainty evidence), however the confidence interval encompasses benefit and harm. TCCMD versus digital non-targeted communication No studies reported STI rates, condom use, ART adherence, abortion rates, or contraceptive use as outcomes for this comparison. TCCMD may increase service utilisation overall (RR: 1.71, 95% CI 0.67-4.38, low certainty evidence), however the confidence interval encompasses benefit and harm and there was considerable heterogeneity (I2 = 72%), with mixed results according to type of service utilisation (STI/HIV testing, and VMMC). Few studies reported on unintended consequences. One study reported that a participant withdrew from the intervention as they felt it compromised their undisclosed HIV status.

Authors' conclusions: TCCMD may improve some outcomes but the evidence is of low certainty. The effect on most outcomes is uncertain/unknown due to very low certainty evidence or lack of evidence. High quality, adequately powered trials and cost effectiveness analyses are required to reliably ascertain the effects and relative benefits of TCC delivered by mobile devices. Given the sensitivity and stigma associated with sexual and reproductive health future studies should measure unintended consequences, such as partner violence or breaches of confidentiality.

Trial registration: ClinicalTrials.gov NCT03117842 NCT02093884 NCT02680613 NCT03122275 NCT03482388 NCT03224390 NCT02872363 NCT03662165 NCT02417233 NCT02905513 NCT02905461 NCT02376023 NCT01761643 NCT01317277 NCT02756949 NCT02579785 NCT03118219 NCT01630304 NCT03478397 NCT02509702 NCT02627365 NCT03082482 NCT03119337 NCT03205982 NCT03253783 NCT03259698 NCT03367130 NCT03394391 NCT03738410 NCT03760211 NCT03928717 NCT02319330.

Publication types

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

MeSH terms

  • Abortion, Legal / statistics & numerical data
  • Adolescent
  • Cell Phone*
  • Communication*
  • Contraception / statistics & numerical data
  • Health Behavior
  • Health Knowledge, Attitudes, Practice
  • Health Services Needs and Demand / statistics & numerical data
  • Humans
  • Quality Improvement
  • Randomized Controlled Trials as Topic
  • Reproductive Health / standards*
  • Sexual Health / standards*
  • Sexually Transmitted Diseases
  • Text Messaging
  • Uncertainty
  • Young Adult

Associated data

  • ClinicalTrials.gov/NCT03117842
  • ClinicalTrials.gov/NCT02093884
  • ClinicalTrials.gov/NCT02680613
  • ClinicalTrials.gov/NCT03122275
  • ClinicalTrials.gov/NCT03482388
  • ClinicalTrials.gov/NCT03224390
  • ClinicalTrials.gov/NCT02872363
  • ClinicalTrials.gov/NCT03662165
  • ClinicalTrials.gov/NCT02417233
  • ClinicalTrials.gov/NCT02905513
  • ClinicalTrials.gov/NCT02905461
  • ClinicalTrials.gov/NCT02376023
  • ClinicalTrials.gov/NCT01761643
  • ClinicalTrials.gov/NCT01317277
  • ClinicalTrials.gov/NCT02756949
  • ClinicalTrials.gov/NCT02579785
  • ClinicalTrials.gov/NCT03118219
  • ClinicalTrials.gov/NCT01630304
  • ClinicalTrials.gov/NCT03478397
  • ClinicalTrials.gov/NCT02509702
  • ClinicalTrials.gov/NCT02627365
  • ClinicalTrials.gov/NCT03082482
  • ClinicalTrials.gov/NCT03119337
  • ClinicalTrials.gov/NCT03205982
  • ClinicalTrials.gov/NCT03253783
  • ClinicalTrials.gov/NCT03259698
  • ClinicalTrials.gov/NCT03367130
  • ClinicalTrials.gov/NCT03394391
  • ClinicalTrials.gov/NCT03738410
  • ClinicalTrials.gov/NCT03760211
  • ClinicalTrials.gov/NCT03928717
  • ClinicalTrials.gov/NCT02319330