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Clinical Trials/NCT01775150
NCT01775150
Unknown
Not Applicable

Using Mobile Phone Text Messaging to Reduce Maternal and Infant Deaths in Remote Rural Areas in China

Ottawa Hospital Research Institute1 site in 1 country5,646 target enrollmentOctober 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bleeding
Sponsor
Ottawa Hospital Research Institute
Enrollment
5646
Locations
1
Primary Endpoint
Neonatal death
Last Updated
13 years ago

Overview

Brief Summary

We plan to integrate WHO educational material using mobile phone text messaging, target on pregnant women in remote rural areas in China. We hypothsized that text messaging can have major impact on reducing maternal and infant deaths in rural China because text messaging is accessible, acceptable, and affordable.

Detailed Description

1. Sampling method: Random sampling method will be used. Counties in Huaihua area of Chinese province of Hunan will be randomly allocated to intervention and non-intervention groups. 2. The intervention: Mobile phone text messages containing maternal and newborn health care education material will be sent to mothers-to-be at the first, second and third trimester, and again postpartum period. 3. Statistical analysis: We will first compare the baseline characteristics (including the average income, adult educational level, and maternal and perinatal mortality rates in the past two years) between the 2 arms of experiment. For costs data, total costs, costs per participating woman, and costs per maternal/infant death avoided will be reported. For primary outcomes, we will determine and report rate ratios, risk differences, and numbers needed to treat (NNT) from the experimental arm (i.e., mobile phone text messaging), using the usual care arm (no text messaging) as the reference. Relative risks and 95% confidence intervals will be expressed as the effect measures. We will estimate the adjusted relative risks and 95% confidence intervals by regression analysis. Mixed models taking consideration of multi-level measures (e.g., mortality and morbidity measured at individual level and intervention measured at village level) will be used in the regression analysis (Donner and Klar, 2000).

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
May 2013
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • women who were registered by local Maternal Child Health unit during the study period

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Neonatal death

Time Frame: 28 days

28 days after birth

Secondary Outcomes

  • Maternal death(300 days)

Study Sites (1)

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