CClinicalTrials.gg
Status unknownNCT02121821Updated Apr 24, 2014

Impact Evaluation of the Pilot SMS Mother Reminder System

An interventional study of SMS reminder messages in Effects of the SMS Mother Reminder System on Use of Health Care., sponsored by African Strategies for Health. Status unknown at 1 site in Uganda. Open to female participants. Per ClinicalTrials.gov, last updated 2014-04-24.

Sponsored by African Strategies for Health · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Apr 2014), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
11,454
Allocation
Randomized
Sex
Female
01

Study summary

The study aims to assess the effects of the SMS Mother Reminder system on use of health care in Uganda. A secondary aim of the study is to determine the behavioral factors and cost-effectiveness, as well as test the usability of the SMS Mother Reminder in Uganda.

Read the detailed description

USAID/Uganda is commissioning a prospective impact evaluation of the initial SMS component of Uganda's National Health Record Program (NHRP) in order to inform strategic targeting of eHealth and future investments after the pilot phase of the NHRP mobile platform "SMS Mother Reminder". This impact evaluation will be designed to answer the following questions:

Primary evaluation question:

  • What is the effect on maternal health outcomes (ANC4 and IPTP2) of the village health teams' use of the SMS Mother Reminder system?

Secondary evaluation questions:

  • What factors most influence changes in health workers, village health teams and expectant women's knowledge, attitudes and practices in maternal health?
  • To what extent is using the SMS Mother Reminder application to track and inform pregnant women a cost-effective intervention from the perspectives of USAID?
  • To what extent can users easily carry out specific tasks (e.g. entering the information of pregnant women) of the SMS Mother Reminder application on mobile devices?

This study is funded by USAID through the African Strategies for Health project.

02

Conditions studied

  • Effects of the SMS Mother Reminder System on Use of Health Care.
03

In context

Lead sponsor

This is the only study on the registry with African Strategies for Health as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Pregnant

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
11,454 participants (estimated)

Study arms

  • No intervention
    Control

    A control group of pregnant women receiving no intervention (i.e. no SMS reminders).

  • Experimental
    SMS reminder messages

    The intervention group will be composed of pregnant women receiving SMS reminder messages via the SMS Mother Reminder system.

    Behavioral: SMS reminder messages

Interventions

  • BehavioralSMS reminder messages

    The study is prospective and interventional comparing differences between pregnant women who receive reminder messages via the SMS Mother Reminder system to those who are not. Pregnant women will be followed from their first ANC visit at a health facility through delivery. The study will examine the effect of the mobile phone intervention on attendance to ANC appointments and IPTP2 coverage. The intervention group will be composed of pregnant women receiving SMS reminder messages in comparison with a control group of pregnant women receiving no intervention (i.e. no SMS reminders).

06

What researchers measure

Primary outcomes

  1. ANC visits

    Pregnant women attend 4 Antenatal care visits (ANC)

    Time frame: 1 year

  2. SP doses

    Pregnant women receive at least 2 doses of intermittent preventive treatment of malaria in pregnancy using sulfadoxine-pyrimethamine (SP).

    Time frame: 1 year

07

Study locations

1 site
  • Gulu District Health Centers
    Gulu, Uganda
    • Donald Shepard, Ph.D. · Contact · shepard@brandeis.edu · +1-781 736-3975
    • Donald Shepard, Ph.D. · Principal investigator
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 24, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02121821
Lead sponsor
African Strategies for Health
Collaborators
United States Agency for International Development (USAID)
Responsible party
Sponsor
First posted
Apr 24, 2014
Start date
May 2014
Primary completion
May 2015 (estimated)
Completion
Sep 2015 (estimated)
Last update
Apr 24, 2014

Study contacts

Lungi Okoko, MPH
Contact
lokoko@as4h.org
+1 703-667-3722
Donald Shepard, Ph.D.
principal investigator · Brandeis University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2014. You cannot join it, but the record below documents what was studied.

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