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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02121821
Other study ID # MSH-001
Secondary ID
Status Not yet recruiting
Phase N/A
First received April 22, 2014
Last updated April 22, 2014
Start date May 2014
Est. completion date September 2015

Study information

Verified date April 2014
Source African Strategies for Health
Contact Lungi Okoko, MPH
Phone +1 703-667-3722
Email lokoko@as4h.org
Is FDA regulated No
Health authority Uganda: Mildmay Uganda research and Ethics Committee (MUREC)
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 11454
Est. completion date September 2015
Est. primary completion date May 2015
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Pregnant

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms

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

Intervention

Behavioral:
SMS 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).

Locations

Country Name City State
Uganda Gulu District Health Centers Gulu

Sponsors (2)

Lead Sponsor Collaborator
African Strategies for Health United States Agency for International Development (USAID)

Country where clinical trial is conducted

Uganda, 

Outcome

Type Measure Description Time frame Safety issue
Primary ANC visits Pregnant women attend 4 Antenatal care visits (ANC) 1 year No
Primary SP doses Pregnant women receive at least 2 doses of intermittent preventive treatment of malaria in pregnancy using sulfadoxine-pyrimethamine (SP). 1 year No