COMPLETED

Father Inclusive Prenatal Care Study

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

Young families need additional institutional support to help them meet the challenges of parenthood. Prenatal clinics are well situated to address some of their needs by expanding services to include fathers. The Father Inclusive Prenatal Care (FIPC) model is designed to prepare young men for the challenges of parenting by supporting the development of their relationship skills as part of routine prenatal healthcare. This approach involves assessing expectant fathers and mothers with a "parent prep-check" (PPC) to identify their needs and then offer services to address those needs and prepare them for parenthood. Services include: (1) parent education about how to understand and care for infants, and how to build secure parent-child bonds; (2) an evidence-based co-parenting program to strengthen and stabilize their family; and (3) educational and employment support designed to help young parents find and keep living wage jobs. The project will be implemented through several community based healthcare sites that are well positioned to engage young fathers through their prenatal clinics. To extend the reach and accessibility of the model, trainings and most services will be available online. As a result of participating in this project it is expected that young couples will have better co-parenting relationships and be better prepared to take care of their infants.

Official Title

Preparing for Parenthood: A Father Inclusive Model of Prenatal Care

Quick Facts

Study Start:2021-06-09
Study Completion:2025-09-29
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05652387

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:17 Years to 29 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Women: pregnant woman
  2. * Men \& women have to be willing to participate at baseline interview together
  1. * Men \& Women: Language other than Spanish or English and cognitive disability interfering with ability to understand the informed consent process.

Contacts and Locations

Principal Investigator

Wrenetha A Julion, PhD, MPH, RN
PRINCIPAL_INVESTIGATOR
Rush University Medical Center
Paul w Florsheim, PhD
PRINCIPAL_INVESTIGATOR
University of Wisconsin, Milwaukee

Study Locations (Sites)

Rush University Medical Center
Chicago, Illinois, 60612
United States

Collaborators and Investigators

Sponsor: Rush University Medical Center

  • Wrenetha A Julion, PhD, MPH, RN, PRINCIPAL_INVESTIGATOR, Rush University Medical Center
  • Paul w Florsheim, PhD, PRINCIPAL_INVESTIGATOR, University of Wisconsin, Milwaukee

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 Date2021-06-09
Study Completion Date2025-09-29

Study Record Updates

Study Start Date2021-06-09
Study Completion Date2025-09-29

Terms related to this study

Keywords Provided by Researchers

  • fatherhood
  • prenatal care
  • coparenting
  • parenting education

Additional Relevant MeSH Terms

  • Antenatal Care
  • Pregnancy Related
  • Parent-Child Relations
  • Parenting
  • Education
  • Counseling