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Today Not Tomorrow Pregnancy and Infant Support Program (TNT- PISP)

Primary Purpose

Infant Mortality, Infant Death, Racial Bias

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Today Not Tomorrrow Pregnancy and Infant Support Program
Sponsored by
University of Wisconsin, Madison
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Infant Mortality focused on measuring TNT-PISP

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Pregnant self- identified black women
  • Living in Dane County Wisconsin

Exclusion Criteria:

  • Not pregnant or did not deliver within the last year
  • Do not self- identify as a black woman

Sites / Locations

  • University of Wisconsin Madison

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

TNT PISP intervention

Control

Arm Description

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.

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.

Outcomes

Primary Outcome Measures

Participant recruitment as assessed by percentage of participants enrolled in Today Not Tomorrow Pregnancy and Infant Support Program (TNT-PISP)
TNT-PISP is aiming to recruit 20 self-identified African American women into the TNT-PISP Pilot. The actual recruitment will be measured as percentage of participants recruited, assuming recruitment of 20 participants per arm as 100%
Retention rate of participants as assessed by percentage of participants adhered to study for 2 years
Retention rate of participants as assessed by percentage of participants adhered to study for 2 years

Secondary Outcome Measures

Preliminary Maternal Child Health Outcomes: Birth weight
Birth weight of baby will be assessed from the medical records in the TNT-PISP group and the control group to assess the effect of the intervention on the preliminary maternal child health outcome.
Preliminary Maternal Child Health Outcomes: Birth gestational age
Birth gestational age will be assessed from the medical records in the TNT-PISP group and the control group to assess the effect of the intervention on the preliminary maternal child health outcome.
Percentage of participants breastfed babies at time of birth
Percentage of participants breastfed babies at time of birth as per the medical records
Percentage of participants opted for inter-conception care plans
Percentage of participants opted for inter-conception care plans as per the medical records
Rate of attendance to 6- week postpartum visit
Rate of attendance to 6- week postpartum visit as per the medical records

Full Information

First Posted
September 19, 2019
Last Updated
September 12, 2022
Sponsor
University of Wisconsin, Madison
Collaborators
Wisconsin Partnership Program
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1. Study Identification

Unique Protocol Identification Number
NCT04100577
Brief Title
Today Not Tomorrow Pregnancy and Infant Support Program (TNT- PISP)
Official Title
Addressing Black Infant Mortality in Wisconsin Through a Collaborative Health Equity Approach Through Community Based Group Prenatal Care and Infant Support
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
October 3, 2019 (Actual)
Primary Completion Date
August 31, 2022 (Actual)
Study Completion Date
August 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Wisconsin, Madison
Collaborators
Wisconsin Partnership Program

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This pilot project aims to implement and investigate the feasibility and acceptability of a unique community based prenatal care and support model for African American women and infants in Dane County. The model, the "Today Not Tomorrow Pregnancy and Infant Support Program (TNT-PISP)" builds on emerging evidence about how to effectively implement and sustain prenatal care in black communities. It combines three approaches-community-based doula programs; group-based models of prenatal care, such as Centering Pregnancy; and community-based pregnancy support groups-into once monthly group sessions held during the prenatal and immediate postpartum period. The project is based at the Today Not Tomorrow Family Resource Center in Madison's East Side Community Center, and carried out in close collaboration with Project Babies, Harambee Village Doulas, and the African American Breastfeeding Alliance of Dane County, Inc.
Detailed Description
Wisconsin leads the nation in the number of African American babies dying before their 1st birthday. These deaths are primarily due to complications of prematurity - babies being born too early and too soon. Additionally, Wisconsin's black infant mortality rate is significantly higher than that of whites and represents a serious health inequity that is critical for local research and advocacy efforts to address. The factors leading to inequities in preterm birth and infant mortality are complex and multifactorial; therefore, multidisciplinary and innovative approaches to prenatal and inter conception care are critical to improve these outcomes. Previous research and feedback from black women living in Dane County has shown that lack of social support and culturally relevant models of preconception, prenatal, and inter-conception care has been a barrier to optimal quality of care and maternal child health outcomes. Further research has demonstrated that evidence based intervention approaches used nationally such as a) community-based doula programs, b) group-based models of prenatal care such as Centering Pregnancy, and c) community-based pregnancy and inter conception support groups hold promise as relevant prevention strategies, yet there are many barriers to their effective adoption in communities of color. In response to the current birth outcome inequities that exist in Wisconsin, the objective of the current proposal is to implement and investigate a novel approach that combines aspects of all three of the above-mentioned evidence-based models and builds upon emerging evidence about how to effectively implement and sustain prenatal care interventions in Black communities: the TNT-PISP. The TNT-PISP approach is based on increasing evidence that models of prenatal care that are community driven, group based, culturally relevant, family centered, and include enhanced social support have the potential to significantly decrease African American prematurity rates and improve other maternal and infant health measures. TNT-PISP is a collaborative community-based support group uniquely designed to serve black women and infants through once monthly group sessions delivered prenatally and in the immediate postpartum period. Each 2 hour TNT-PISP session will be held at the Today Not Tomorrow Family Resource Center located on Madison's Eastside and will be led by local African American community-based doulas supported by and in collaboration with a host of other community partners and healthcare professionals from diverse backgrounds. Each session will consist of food, hands on learning activities, peer to peer socio-emotional support, guest speakers, relationship building activities, and dynamic discussions on a host of pregnancy and newborn care related topics. In addition to group sessions, participants will be additionally have the option to be enrolled in a community based doula program to receive support outside the group sessions, and culturally sensitive mental health and case management support services on an as-needed basis. Via partnerships with various healthcare providers and systems, there are also tentative plans for future expansion so that select participants will additionally be able to receive their prenatal care exams on site. Assessments with individual participants in each study arm will occur at three contact points: At start of pregnancy, around time of birth/early postpartum and ~ 6 months postpartum. At each time of contact, they will be asked to complete a series of questionnaires and participate in a semi-structured interview with PI. If additionally consented, medical records of all study participants will be analyzed to assess secondary outcomes. This is a pilot study. As the study transition to larger scale efficacy trials in future, it will be important to be able to link to and review patient perinatal outcomes. Feasibility questions asked in this study are 1) Will it be obvious who meets and who does not meet our eligibility criteria? Are the eligibility criteria sufficient or too restrictive? 2) Will our study questionnaires and data collection tools be easy to understand and user friendly? 3) What systems levels facilitators and barriers will contribute to the implementation and success of this pilot program? 4) Will participants be pleased with the curriculum/design of the TNT-PISP pilot intervention? Is delivering prenatal care on site something participants would find beneficial in addition to group education/support sessions? 5) Will our team have the capacity to implement and maintain the TNT-PISP program? Part of the feasibility trial of this study is assessing how receptive mothers are to us accessing their medical records and data retrieval logistics. Additionally, semi structured interviews with up to 10 key academic/community based stakeholders involved in the implementation process of TNT-PISP program will be obtained and evaluated via thematic analysis. Interviews with these key stakeholders will not be compensated and will be on a volunteer basis. These interviews will collect information on the facilitators and barriers to implementing and maintaining the program from their standpoint. Finally, two focus groups will occur over the course of the study period. The first focus group will involve self-identified black women living in Dane County interested in providing feedback on the ideal design of a culturally relevant community based prenatal care and support program such as the TNT-PISP pilot. The second focus group will be limited to research participants who participated in the TNT PISP intervention for at least 1 session and will provide feedback on facilitators and barriers to its acceptability and feasibility as well as preliminary feedback on maternal child health outcomes and attitudes impacted as a result of the program. All individuals involved in conducting one on one interviews/focus groups will be women of color on the research team to facilitate comfort and trust for the participants. All focus groups and individual interviews will be audio recorded. One on one interviews will occur either on the phone or at a comfortable public location of the subject's desire (ex: library or at the TNT Family Resource Center). One on one interviews will take place in a private room to ensure as much privacy as possible. Subjects will also have the option for the interview to occur in their home and if that occurs, they will be made aware that the interviewer is a mandatory reporter if any concerning activities in the home were to be observed. The focus groups will take place at the TNT-Family Resource Center. All one on one interviews will be conducted by Dr. Zapata. All focus groups will be conducted by Dr. Zapata in collaboration with other research team members listed in the protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infant Mortality, Infant Death, Racial Bias, Prenatal Stress, Prenatal Care, Maternal Child Health, Health Problems in Pregnancy, Adverse Childhood Experiences, Mental Health, Support Groups, Minority Health, Healthcare Disparities, Maternal-child Health Services, Social Determinants of Health, Trust, Physician-Patient Relations, Quality of Care
Keywords
TNT-PISP

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A longitudinal, quasi-experimental design with two study arms will be used. Study arm 1 will consist of self-identified pregnant black women who are enrolled in the TNT-PISP intervention and Study arm 2 will consist of self-identified pregnant black women who are not enrolled in the TNT-PISP intervention. During the recruitment process, potential study participants will be able to self- select which study arm they would like to be in after each arm is described in detail. Although self-selection is traditionally discouraged in research, given the vulnerable population the investigator will be working with and historic distrust with medical community, investigator believe there is power in giving women of color choice in how they wish to navigate and engage with this study.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TNT PISP intervention
Arm Type
Experimental
Arm Description
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.
Arm Title
Control
Arm Type
No Intervention
Arm Description
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.
Intervention Type
Other
Intervention Name(s)
Today Not Tomorrrow Pregnancy and Infant Support Program
Intervention Description
The Today Not Tomorrow Pregnancy and Infant Support Program (TNT-PISP) is a collaborative community-based support group uniquely designed to serve black women and infants through once monthly group sessions delivered prenatally and in the immediate postpartum period.
Primary Outcome Measure Information:
Title
Participant recruitment as assessed by percentage of participants enrolled in Today Not Tomorrow Pregnancy and Infant Support Program (TNT-PISP)
Description
TNT-PISP is aiming to recruit 20 self-identified African American women into the TNT-PISP Pilot. The actual recruitment will be measured as percentage of participants recruited, assuming recruitment of 20 participants per arm as 100%
Time Frame
2 years
Title
Retention rate of participants as assessed by percentage of participants adhered to study for 2 years
Description
Retention rate of participants as assessed by percentage of participants adhered to study for 2 years
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Preliminary Maternal Child Health Outcomes: Birth weight
Description
Birth weight of baby will be assessed from the medical records in the TNT-PISP group and the control group to assess the effect of the intervention on the preliminary maternal child health outcome.
Time Frame
At child birth or at 38 week average gestation time whichever will come first
Title
Preliminary Maternal Child Health Outcomes: Birth gestational age
Description
Birth gestational age will be assessed from the medical records in the TNT-PISP group and the control group to assess the effect of the intervention on the preliminary maternal child health outcome.
Time Frame
At child birth or at 38 week average gestation time whichever will come first
Title
Percentage of participants breastfed babies at time of birth
Description
Percentage of participants breastfed babies at time of birth as per the medical records
Time Frame
up to 2 years
Title
Percentage of participants opted for inter-conception care plans
Description
Percentage of participants opted for inter-conception care plans as per the medical records
Time Frame
2 years
Title
Rate of attendance to 6- week postpartum visit
Description
Rate of attendance to 6- week postpartum visit as per the medical records
Time Frame
6 week postpartam

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Pregnant self- identified black women Living in Dane County Wisconsin Exclusion Criteria: Not pregnant or did not deliver within the last year Do not self- identify as a black woman
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jasmine Y Zapata, MD, MPH
Organizational Affiliation
University of WI School of Medicine and Public Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Wisconsin Madison
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53792
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Today Not Tomorrow Pregnancy and Infant Support Program (TNT- PISP)

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