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Faith Leaders Advocating for Maternal Empowerment (FLAME)

Faith Leaders Advocating for Maternal Empowerment (FLAME)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04039932
Enrollment
18
Registered
2019-07-31
Start date
2018-06-01
Completion date
2019-12-31
Last updated
2021-10-27

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

Conditions

Maternal Health Services, Perinatal Care, Prenatal Care

Brief summary

In 2015, the average Ethiopian woman had a 1 in 64 lifetime risk of death due to complications of childbirth and 87,414 newborns died before their 28th day of life. Demand for MNCH services, however, remains low in Ethiopia's rural communities most at risk with only 16% of women delivering in a health facility. The investigator's project responds to the challenge of creating demand for existing MNCH services in rural Ethiopia, which fell short of reaching Millennium Development Goal targets for reducing preventable maternal and neonatal deaths. This study addresses two strategic drivers to prevent maternal mortality identified by USAID including improving individual, household, and community behaviors and norms and increasing equity of access and use of services by the most vulnerable. The primary objective of the study is to determine the impact of a behavior change intervention that partners Ethiopian Orthodox priests with members of the Health Development Army (HDA) and trains them to conduct maternal health outreach to increase births attended by skilled health personnel among women who attend ≥1 ANC visits.

Interventions

BEHAVIORALFLAME

The FLAME intervention trains pairs of faith leaders and community health workers and deploys them to conduct behavior change outreach in their communities.

Sponsors

University of Gondar
CollaboratorOTHER
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Cluster randomized trial assigning facility catchment areas to intervention vs. standard of care

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Pregnant women * Willing to receive intervention counseling

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Facility deliveryThrough study completion, an average of 18 monthsThe proportion of births attended by skilled health personnel among the women who attended ≥1 ANC visits

Secondary

MeasureTime frameDescription
Any ANCThrough study completion, an average of 18 monthsNumber of women who attended ≥1 ANC visits
Complete ANCThrough study completion, an average of 18 monthsNumber of women who attended ANC 4

Countries

Ethiopia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026