Maternal Mortality Clinical Trial
— EWHOfficial title:
Enhancing All Community Health Workers on Maternal and Newborn Health: Rorya Tanzania
NCT number | NCT03024905 |
Other study ID # | 108026 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 16, 2017 |
Est. completion date | May 2019 |
Verified date | August 2019 |
Source | Bruyere Research Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this trial is to establish if several interventions will help women in rural Tanzania access health care services during pregnancy and at the time of delivery. The interventions include education about the importance of attending antenatal care visits with nurses and facility deliveries, a voucher for transport to access the health facility at the time of delivery, and supplies to be used either at the health facility, or on route if the women does not make it to the health facility.
Status | Completed |
Enrollment | 17000 |
Est. completion date | May 2019 |
Est. primary completion date | May 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: 1. Women must be pregnant. 2. Women must live in Rorya District, but not in Shirati Town. 3. Women must deliver in Rorya District . Exclusion Criteria: 1. Women who live outside or deliver outside of Rorya District. 2. Women who deliver preterm, before they have exposure to all the interventions. |
Country | Name | City | State |
---|---|---|---|
Tanzania | Shirati District Hospital Research Office | Shirati, Rorya District | Mara Region |
Lead Sponsor | Collaborator |
---|---|
Bruyere Research Institute | Ottawa Hospital Research Institute, Shirati KMT Hospital |
Tanzania,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Facility births | Number of women attending health facilities for delivery | During baseline vs during intervention periods until end of study (2 years) | |
Secondary | Antenatal Care visits | Number of times women attend health facility for antenatal visits | During baseline vs during intervention until end of study (2 years) | |
Secondary | Postpartum visits | Number of women attending health facility for postpartum visits | During baseline vs during intervention until end of study (2 years) | |
Secondary | Use of transport intervention | Number of women using the free transport intervention | During Intervention until end of study (2 years) | |
Secondary | Use of birth kit | Number of women using the birth kit | During Intervention until end of study (2 years) |
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