An mHealth Strategy to Reduce Pre-Eclampsia and Infant Death in Tanzania
Pre-Eclampsia, Eclampsia, Hypertension, Pregnancy-Induced
About this trial
This is an interventional health services research trial for Pre-Eclampsia focused on measuring Pre-eclampsia, Eclampsia, mHealth, mobile health, Gestosis, Hypertension, Pregnancy-Induced
Eligibility Criteria
Inclusion Criteria:
- at least 5 months pregnant
Exclusion Criteria:
- Unable to provide consent.
Sites / Locations
- Ifakara Health Institute
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Intervention Arm
Enhanced Usual Care
Community-based Pre-eclampsia/Eclampsia Detection and Management Strengthened Referral Network from Community to Referral hospital levels Antenatal Care Nurses will receive training on best practices for PE detection and management per Tanzanian Standard Treatment Guidelines. Antenatal Care Nurses will be given smartphones and will be trained to complete Case Report Forms (CRF) to log key indicators and activities at each ANC visit, delivery and Postnatal Care visits of enrolled participants. Antenatal Care Nurses will receive bluetooth blood pressure monitors. Community Health Workers within the intervention arm facilities will receive training in pre-eclampsia features and will be provided with smart phones and access to a smart phone application that will prompt them to initiate follow ups with pregnant women within the community and they will receive SMS/text messages reminders about pregnant women within the community who require follow up.
Antenatal Care Nurses will receive training on best practices for PE detection and management per Tanzanian Standard Treatment Guidelines. Antenatal Care Nurses will be given smartphones and will be trained to complete Case Report Forms (CRF) to log key indicators and activities at each ANC visit, delivery and Postnatal Care visits of enrolled participants. Antenatal Care Nurses will receive bluetooth blood pressure monitors.