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Today Not Tomorrrow Pregnancy and Infant Support Program for Minority Health
N/A
Waitlist Available
Led By Jasmine Y Zapata, MD, MPH
Research Sponsored by University of Wisconsin, Madison
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights
Study Summary
This trial project will provide African American women with prenatal care and support through community-based doulas, group-based prenatal care, and community-based pregnancy support groups.
Eligible Conditions
- Minority Health
- Maternal-Child Health Services
- Trust
- Maternal Child Health
- Support Groups
- Quality of Care
- Prenatal Stress
- Mental Health
- Sudden Infant Death Syndrome
- Prenatal Care
- Infant Mortality
- Racial Bias
- Pregnancy Complications
- Adverse Childhood Experiences
- Healthcare Inequalities
- Social Determinants of Health
- Physician-Patient Relationship
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Participant recruitment as assessed by percentage of participants enrolled in Today Not Tomorrow Pregnancy and Infant Support Program (TNT-PISP)
Retention rate of participants as assessed by percentage of participants adhered to study for 2 years
Secondary outcome measures
Percentage of participants breastfed babies at time of birth
Percentage of participants opted for inter-conception care plans
Preliminary Maternal Child Health Outcomes: Birth gestational age
+2 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: TNT PISP interventionExperimental Treatment1 Intervention
Participants in TNT PISP intervention group will come to once monthly educational support group sessions and will be additionally enrolled in the community based doula program where they will receive 1 on 1 doula and lactation support throughout their pregnancy, delivery, and postpartum period. They will receive prenatal care clinical visits on their own with their prenatal care provider. In phase 2 of the study, participants will be offered on site prenatal care once per month.
Group II: ControlActive Control1 Intervention
Participants in control group will have no enhanced prenatal care support. They will attend visits on their own with their prenatal care provider and participation in this research study will not interfere with the prenatal care.
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Who is running the clinical trial?
Wisconsin Partnership ProgramOTHER
7 Previous Clinical Trials
434 Total Patients Enrolled
University of Wisconsin, MadisonLead Sponsor
1,182 Previous Clinical Trials
3,167,363 Total Patients Enrolled
Jasmine Y Zapata, MD, MPHPrincipal InvestigatorUniversity of WI School of Medicine and Public Health
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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