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SURVIVAL PLUSS: Increasing Capacity for Mama-baby Survival in Post-conflict Uganda and South Sudan

SURVIVAL PLUSS: Increasing Capacity for Mama-baby Survival in Post-conflict Uganda and South Sudan

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02605369
Enrollment
1877
Registered
2015-11-16
Start date
2018-01-03
Completion date
2019-02-28
Last updated
2023-10-10

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

Conditions

Low Birthweight, Neonatal Death, Neonatal Hypoglycemia, Preterm Birth

Keywords

Facility births

Brief summary

Universal coverage of good quality facility based care globally could prevent nearly 113,000 maternal deaths, 531,000 stillbirths and 1.3 million neonatal deaths annually by 2020. Yet, only 57% of pregnant Ugandan women choose to deliver at health facilities. This unacceptably low coverage of facility based births could explain, in part, the high maternal and perinatal mortality estimates in Uganda. While multiple studies have examined factors associated with this low utilization of health services around the time of birth, there is inadequate implementation research exploring the best systematic methods that could promote uptake and scale up of facility based births. This study will therefore examine the effect of an intervention package (peer counselling by pregnancy buddies on facility based births, mobile phone messaging promoting facility based births and provision of mama-kits) on the frequency of facility based births and perinatal mortality. The study, a cluster randomized community based intervention trial in post-conflict Northern Uganda, will provide data crucial in framing national policy regarding measures to promote the use of health facilities.

Interventions

BEHAVIORALIntervention arm: An integrated package

See description in previous column

Sponsors

Centre For International Health
CollaboratorOTHER
Makerere University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women at 28 or more weeks of gestation * Residence in the selected clusters * Pregnant women under 18 years of age will be included since they are considered as emancipated minors in Uganda

Exclusion criteria

* Intention to move from the study area within one year * Psychiatric ailments that may inhibit the informed consent process

Design outcomes

Primary

MeasureTime frameDescription
Facility based birthDay 1Delivery at a health facility

Secondary

MeasureTime frameDescription
Timely initiation of breastfeedingUp-to one hour after birthInitiation of breastfeeding with the first hour after birth
Severe illnessDay 28Severe illness within the first month of life
The percent of newborns attended by a health care pro-vider during the first 48 hours following birthUp-to 48 hours after birthProportion of babies seen by a health care work in the first 48 hours after birth
The percent of newborns attended by a health care pro-vider during the first 7 days following birth1 weekProportion of babies seen by a health care work in the first one week after birth
Neonatal deathDay 28Death within the first month of life

Other

MeasureTime frameDescription
Neonatal hypoglycemiaUp-to 7 days after birthProportion of infants with random blood glucose less than 47mg/dl
Preterm birth7 days postpartumProportion of infants born at less than 37 completed weeks of gestation measured by the New Ballad Score
Low birthweightUp-to 48 hours after birthProportion of infants with a birthweight =\< 2500gms

Countries

Uganda

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026