Understanding the Role of Doulas in Supporting People With PMADs
University of Montana · NCT05763537
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 75
- US sites recruiting
- 1
- Study start
- November 26, 2024
- Record last updated
- August 14, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Standard Doula Care Plus PMAD Intervention; Standard Doula Care
Conditions: Maternal Health; Pregnancy; Delivery, Obstetric; Self Efficacy; Social Support; Mental Health; Substance-Related Disorders; Postpartum Depression; Depression; Mental Health Services
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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
Exclusion Criteria
- 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.
Recruiting US locations
University of Montana
Missoula, MT 59812
Site contact: Jessica L Liddell, PhD · 4357576780 · jessica.liddell@mso.umt.edu
Study contacts (from the official record)
- Jessica L Liddell, PhD · 4357576780 · jessica.liddell@mso.umt.edu
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