About this trial
Detailed Description The doula-led intervention developed during the first phase of this project will be pilot tested for feasibility. Following the recruitment procedures described in the recruitment and retention plan, approximately 75 participants will be enrolled into the study. Twenty-five of the participants will receive regular doula care and 25 of the participants will receive care from a doula trained in the PMAD doula training throughout their pregnancy, childbirth, and postpartum time period, following the intervention procedures developed in Aim 2 of this study. Twenty-five women will not receive care from a doula and will receive perinatal care as usual. Women in all groups will take surveys via REDCap during their enrollment in the intervention, at 1 month postpartum, 3 months, and 6 months postpartum (at the conclusion of the intervention). All participants who receive the PMAD doula intervention will complete checklists after each session with their doula, to assess fidelity to the intervention. Participant communication with their doula via patient notebook will also be assessed for fidelity to the intervention.
Eligibility criteria
Qualifiers
Participants must be over the age of 18
Currently pregnant and between 13 and 26 gestational weeks at the time of enrollment
Live in a HRSA-designated rural area of Montana
Disqualifiers
They are under the age of 18
Not currently pregnant
Not between 13-26 gestational weeks at the time of enrollment
If they do not live in a HRSA-designated rural are of Montana.
Trial design
Treatments tested in this trial
- Standard Doula Care Plus PMAD Intervention
- Standard Doula Care