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Reduction of Adverse Pregnancy Outcomes With a Smartphone Application in Ghana

Reduction of Adverse Pregnancy Outcomes With a Smartphone Application in Ghana: a Cluster Randomized Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02185625
Enrollment
3773
Registered
2014-07-09
Start date
2014-07-31
Completion date
2014-09-30
Last updated
2016-05-19

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

Conditions

Delivery, Obstetric, Infant Mortality, Midwifery, Postpartum Hemorrhage, Stillbirth

Brief summary

The purpose of this study is to determine whether use of the Safe Delivery smartphone application by midwives can reduce excess blood loss from bleeding, and infant death during childbirth in Ghanaian women. Moreover, it will be investigated whether the Safe Delivery application can increase midwives' knowledge and skills in managing childbirth. Fifteen hospitals in Greater Accra, Ghana, will be cluster randomized to either use the Safe Delivery application (intervention), or to no intervention (control). In the intervention hospitals, midwives will be educated in the use of Safe Delivery. Pregnant women will be enrolled at delivery and followed until 7 days postpartum. Data collection will begin July 2014 and is expected to be finished by October 2014.

Interventions

The intervention is the use of a smartphone application called Safe Delivery, designed by University of Copenhagen, Denmark and Maternity Foundation Denmark. The application contains animated videos aimed to train midwives in the prevention and management of postpartum hemorrhage and the treatment of neonatal resuscitation. The instructions in the videos are based on WHO recommendations, and the application is designed to be an on-going tool for midwives, so that they can drill themselves in the emergencies of postpartum hemorrhage and neonatal resuscitation.

Sponsors

University of Copenhagen
CollaboratorOTHER
University of Ghana
CollaboratorOTHER
Maternity Foundation
CollaboratorUNKNOWN
Augustinus Fonden
CollaboratorOTHER
Lundbeck Foundation
CollaboratorOTHER
Edith and Godtfred Kirk Christiansen Foundation
CollaboratorUNKNOWN
Aase and Ejnar Danielsens Foundation
CollaboratorOTHER
University of Aarhus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

for Hospitals: * Located in the region of Greater Accra. * The hospital should have at least 10 midwives employed. * The patient flow for each midwife should be at least 10 deliveries per month. * The annual average number of deliveries should be at least 1,200. Inclusion criteria for midwives: * Should have no leave or vacation from June 17th to September 17th 2014. * Should have a full time employment at the delivery ward (conducting deliveries 100% of the work time). * Should be willing and available to participate in an information meeting at the hospital where the balloting among eligible midwives will take place. * Should give an informed consent to participate in the study. * Should be willing and available to participate in a workshop July 14th 2014 (this is the day of randomization, and intervention midwives will receive smartphone training). * Should be willing and available to participate in a workshop September 17th 2014 (to complete an end of study questionnaire, the key feature questionnaire, and control midwives will receive smartphones). * Should be proficient in English to understand the spoken instructions in the animated videos. Inclusion criteria for women in labor: * Should be in active labor. * Should give informed consent to participate in the study. * Should give birth vaginally. The women in labor and their newborn children will be the primary observational units.

Design outcomes

Primary

MeasureTime frameDescription
Postpartum Hemorrhage.Measurements 2 hours after delivery.Postpartum Hemorrhage is defined as blood loss greater than 500 ml from bleeding associated with childbirth within first 2 hours postpartum.

Secondary

MeasureTime frameDescription
Blood lossMeasurements 2 hours after delivery.Amount of blood loss (ml) from bleeding associated with childbirth within first 2 hours postpartum.
Key feature questionnaire (KFQ).At baseline and 2 months after randomization.The KFQ questionnaire measures midwives' knowledge in relation to 1) active management of the third stage of labour, 2) treatment of postpartum hemorrhage, 3) manual removal of placenta, and 4) neonatal resuscitation. The midwives' performance will be scored by research assistants by use of the KFQ tool.
Objective structured assessment of technical skill (OSATS).At baseline and 2 months after randomization.The OSATS tool measures midwives' skills in relation to 1) active management of the third stage of labour, 2) treatment of postpartum hemorrhage, 3) manual removal of placenta, and 4) neonatal resuscitation. The midwives' performance will be scored by research assistants by use of the OSATS tool.
Fresh stillbirthAt delivery.Delivery of a fetus with a birth weight above 1,000 g birth weight who at birth has no signs of life (breathing, crying or movement) with intact skin.
Neonatal mortality 7 days postpartum.Within 7 days postpartum.A baby born alive with a birth weight above 1000 g who dies within 7 days postpartum.

Countries

Ghana

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026