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Interconception Care at the University of Mississippi Medical Center

NCT03024385 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 1625

Last updated 2020-04-27

No results posted yet for this study

Summary

This model will utilize tools from the IMPLICIT (Interventions to Minimize Preterm and Low Birth Weight Infant through Continuous Quality Improvement Techniques) Network (collaboration of academic family medicine providers). The project involves assessing maternal risk behaviors that significantly affect subsequent birth outcomes: specifically smoking cessation, maternal depression, family planning and preconception folic acid supplementation during well child (WCC) visits. There is evidence that screening mothers for depression can be done at WCC. Data from IMPLCIT network has demonstrated increased screening and referral rates as well as decreased rates of prematurity. This is the first collaborative effort between Pediatrics and Family Medicine.

Conditions

Interventions

BEHAVIORAL

Well Child Visits

Mothers of young infants will be screened for maternal behaviors that affect the outcome of future pregnancies. These behaviors are related to the following: family planning; smoking status, prenatal vitamin use and maternal depression. Mothers with positive screens will be offered appropriate resources. This will all take place during the child's routine well-child visit.

Sponsors & Collaborators

  • IMPLICIT Network

    collaborator UNKNOWN

  • March of Dimes

    collaborator OTHER

  • University of Mississippi Medical Center

    lead OTHER

Principal Investigators

  • Sarah MH Jones, MD · University of Mississippi Medical Center

Eligibility

Min Age
13 Years
Max Age
67 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-03-20
Primary Completion
2025-01-31
Completion
2026-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03024385 on ClinicalTrials.gov