Exploring how doulas help people with perinatal mood and anxiety disorders
Understanding the Role of Doulas in Supporting People With PMADs
This study is testing whether having a specially trained doula can help people dealing with mood and anxiety issues during and after pregnancy feel better.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 75 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | University of Montana Academic / other |
| Locations | 1 site (Missoula, Montana) |
| Trial ID | NCT05763537 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of doula support for individuals experiencing perinatal mood and anxiety disorders (PMADs) during pregnancy and postpartum. Approximately 75 participants will be enrolled, with some receiving standard doula care and others receiving specialized care from doulas trained in PMAD support. Participants will complete surveys at various intervals to assess their experiences and outcomes. The study aims to gather data on the feasibility of the intervention and its impact on maternal health.
Who should consider this trial
Good fit: Ideal candidates are pregnant individuals aged 18 and older, between 13 and 26 weeks of gestation, residing in rural areas of Montana.
Not a fit: Patients who are not currently pregnant or do not live in designated rural areas of Montana may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance support for individuals with PMADs, leading to improved maternal mental health outcomes.
How similar studies have performed: Previous studies have shown positive outcomes with doula support in maternal health, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion 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.
Where this trial is running
Missoula, Montana
- University of Montana — Missoula, Montana, United States (Recruiting)
Study contacts
- Study coordinator: Jessica L Liddell, PhD
- Email: jessica.liddell@mso.umt.edu
- Phone: 4357576780
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.