RECRUITING

Midwest Birth Outcomes and Indigenous American Pregnancy

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Indigenous American pregnancies in the Midwest have disproportionally high rates of adverse outcomes, however little research has been done on how historical trauma and stress may impact these adverse outcomes. This project gathers data from pregnant Indigenous American women on their experiences with historical trauma, stress, and birth outcomes, as well as physiological data of how they respond to stress, in order to better understand the associations between these factors and the biological mechanisms underlying them. Understanding the mechanisms by which both historical and proximal stress "get under the skin" and influence pregnancy health and perinatal outcomes, will afford new targets of intervention to help reduce these IA health disparities.

Official Title

Midwest Birth Outcomes and American Indian Pregnancy: Associations With Historical Trauma and Psychosocial Stress

Quick Facts

Study Start:2023-10-31
Study Completion:2025-11-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06008561

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * At least 18 years old
  2. * Less than 26 weeks
  3. * Healthy single baby pregnancy
  4. * Indigenous American
  1. * Assistive reproductive technology (in-vitro fertilization)
  2. * Have a history of cardiac and endocrine disease

Contacts and Locations

Study Contact

Valentina Ayala Catalan
CONTACT
6053126406
strahmlab@sanfordhealth.org

Principal Investigator

Anna M Strahm, PhD
PRINCIPAL_INVESTIGATOR
Sanford Health

Study Locations (Sites)

Sanford Health
Fargo, North Dakota, 58104
United States
Sanford Health
Sioux Falls, South Dakota, 57104
United States

Collaborators and Investigators

Sponsor: Sanford Health

  • Anna M Strahm, PhD, PRINCIPAL_INVESTIGATOR, Sanford Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-10-31
Study Completion Date2025-11-30

Study Record Updates

Study Start Date2023-10-31
Study Completion Date2025-11-30

Terms related to this study

Additional Relevant MeSH Terms

  • Pregnancy