Understanding pregnancy outcomes in Indigenous American women in the Midwest
Midwest Birth Outcomes and American Indian Pregnancy: Associations With Historical Trauma and Psychosocial Stress
This study looks at how stress and past trauma affect pregnancy outcomes for Indigenous American women in the Midwest to help improve their health and reduce issues like preterm births and infant mortality.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Sanford Health Academic / other |
| Locations | 2 sites (Fargo, North Dakota and 1 other locations) |
| Trial ID | NCT06008561 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on the pregnancy experiences of Indigenous American women in the Midwest, particularly examining how historical trauma and stress impact adverse pregnancy outcomes. By collecting data on the women's experiences with trauma, stress, and physiological responses, the study aims to uncover the biological mechanisms that contribute to high rates of infant mortality and preterm births in this population. The findings could lead to targeted interventions to address these health disparities and improve perinatal health outcomes for Indigenous American women.
Who should consider this trial
Good fit: Ideal candidates for this study are Indigenous American women who are at least 18 years old and less than 26 weeks pregnant with a healthy single baby.
Not a fit: Patients who have undergone assistive reproductive technology or have a history of cardiac and endocrine disease may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights that lead to improved interventions and support for Indigenous American women during pregnancy, ultimately reducing adverse outcomes.
How similar studies have performed: While there is limited research specifically addressing this population, studies focusing on psychosocial stressors and pregnancy outcomes have shown promise in other contexts, indicating potential for success in this novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * At least 18 years old * Less than 26 weeks * Healthy single baby pregnancy * Indigenous American Exclusion Criteria: * Assistive reproductive technology (in-vitro fertilization) * Have a history of cardiac and endocrine disease
Where this trial is running
Fargo, North Dakota and 1 other locations
- Sanford Health — Fargo, North Dakota, United States (Recruiting)
- Sanford Health — Sioux Falls, South Dakota, United States (Recruiting)
Study contacts
- Principal investigator: Anna M Strahm, PhD — Sanford Health
- Study coordinator: Grace Biermann, MPH
- Email: strahmlab@sanfordhealth.org
- Phone: 6053126457
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.