Health Condition 1: O149- Unspecified pre-eclampsia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Women who have pre-eclampsia, their significant others, and healthcare personnel caring for such women will be included in Focus Group Discussions for the development of Shared Decision making tools. In the second phase of the study, the impact of the developed tools will be evaluated in clinical situations by involving women with pre-eclampsia and healthcare personnel.
Exclusion criteria
Exclusion criteria: Women/ patients who do not have pre-eclampsia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| In pregnant women with lived experience of pre-eclampsia, effectiveness of the education and SDM tools, particularly with respect to timing of birth, will be measured using the Ottawa decisional conflict self report scale. Interaction tests will be used to look at differences in effect in different sub-groups (gestational age at time of intervention, parity, ethnicity, setting)Timepoint: End of the study (at 1 year) | — |
Secondary
| Measure | Time frame |
|---|---|
| Post-intervention surverys will access acceptability amongst all participantsTimepoint: End of the study (1 year) | — |
Countries
India, Sierra Leone, Zambia
Contacts
BVVS S Nijalingappa Medical College and HSK Hospital and Research Centre