Skip to content

Point-of-Delivery Prenatal Test Results Through mHealth to Improve Birth Outcome

Point-of-Delivery Prenatal Test Results Through mHealth to Improve Birth Outcome

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03027258
Acronym
mHealth
Enrollment
300
Registered
2017-01-23
Start date
2016-09-30
Completion date
2018-01-31
Last updated
2017-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatitis B, HIV, Sickle Cell Disease

Keywords

Mobile health technology

Brief summary

The investigators propose to adopt sustainable community networks (in this case churches) to implement an integrated community-based screening that incorporates mobile health technology (mHealth) to make prenatal test results available at the point-of-delivery to guide medical management.

Detailed description

The investigators will develop and test the feasibility, acceptability, and usability of a mobile health platform that captures results for HIV, Hepatitis B virus (HBV) and sickle cell genotype obtained from participants during the Healthy Beginning Initiative (HBI) program; store data in a secure, web-based database; encrypt data on a smart card which is given to participants, and make these data available at the point-of-delivery using a cell-phone application to read the smart card. Data on the web-based database can also be accessed directly using the cell phone application. Evidence exists that when clinician have maternal records available at the point of delivery, they are more likely to initiate antiretroviral prophylaxis for HIV-exposed infants, administer the first dose of hepatitis B vaccine with 24 hours for infants born to women who have positive hepatitis B surface antigen and screen infants born to mothers with sickle cell trait to allow early identification and initiation of penicillin prophylaxis for infants who have sickle cell disease.

Interventions

OTHERmHealth

HBI participants who consent will be enrolled in this study and will have data collected from their community screening stored in a secure, web-based database. The stored data will be encrypted into a Quick Response code embedded in a smart card. A unique identification number and participant's blood group type will be on the outside of the card. There will be no names or any other identifiers. Each participating center will identify a dedicated delivery room staff that will be trained to read the contents of the card using the cell phone application as well as enter new data in the participant's profile. When a participant presents at delivery without the card, information can still be obtained from the secure, web-based database and confirmed using the participant's name, date of birth and cell phone number. This information is provided to the clinician to guide management of the infant.

Sponsors

Fogarty International Center of the National Institute of Health
CollaboratorNIH
University of Nevada, Las Vegas
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women; 18 years or older enrolled in the Healthy Beginning Initiative * One of the three conditions - HIV, Hepatitis B, and Sickle cell trait/disease

Exclusion criteria

* Those who do not accept to have their information uploaded on the secure database

Design outcomes

Primary

MeasureTime frameDescription
Reach6 monthsReach will be calculated as: the proportion of enrolled pregnant women relative to eligible pregnant women in the study catchment area.
Effectiveness6 monthsEffectiveness will be determined by assessing the impact of the mHealth platform on key outcomes such as screening for HIV, HBV, and sickle cell genotype, and health care utilizations for follow up visits. This will be measured by calculating the percentage of pregnant women that used the smart card at the point-of-delivery.
Adoption6 monthsAdoption rates will be calculated using the proportion of interested health care settings to the total number eligible for participation.
Acceptability6 monthsThe proportion of enrolled pregnant women who accept to use the smart card for their health care services

Countries

Nigeria

Contacts

Primary ContactEchezona Ezeanolue, MD, MPH
echezona.ezeanolue@unlv.edu7028952687
Backup ContactSemiu O Gbadamosi, MD, MPH
semiu.gbadamosi@unlv.edu7028351946

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026