Testing the Effectiveness of the Her Health Program to Add Healthcare Value in the Fourth Trimester
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Her Health Program.
- Who it may be relevant to
- Registry conditions: Postpartum, Pregnancy Related. Basic parameters: from 16 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The goal of this clinical trial is to learn if a program Woman's Hospital has made, called the Her Health Program, can help women be healthy and get healthcare in the first year after having a baby. The main question\[s\] the study aims to answer are: * Can the Her Health program increase access to healthcare in the first year postpartum? * Can the Her Health program increase knowledge about healthcare and change feelings toward the healthcare system? Participants will complete one research visit in which they will be enrolled and told which group they will be in- "Her Health Program" group or "Usual Care" group. If they are placed in the "Her Health Program" group, they will receive their usual care + the addition of an extra healthcare team member(called a community health navigator) to to work with patients and care team for a year postpartum. Researchers will compare those who receive the Her Health Program and those who do not receive the program to see if the Her Health Program can help women get healthcare in the first year after having a baby.
Interventions
- Behavioral Her Health Program
Addition of a community health worker navigator to assist subject in navigating their health in the first year postpartum.
Primary outcome measures
- Postpartum visit attendance [Time frame: 12 weeks postpartum]
Secondary outcome measures (4)
- Medical trust [Time frame: 12 months postpartum]
- Health literacy [Time frame: 12 months postpartum]
- Self-efficacy [Time frame: 12 months postpartum]
- Healthcare costs [Time frame: 12 months postpartum]
Eligibility criteria
Inclusion criteria
- At least 16 years old at the time of consent.
- Gave birth within 7 days before randomization
- Medicaid enrolled
- Address of residence within a disadvantaged area (ADI>5).
- Clearly understands the study procedures and visit schedule, alternative treatments, and risks involved with the study, and voluntarily agrees to participate by giving verbal and written informed consent
Exclusion criteria
- Use of private health insurance exclusively
- Does not speak English.
- Plans to move out of state during the study time period
- Unwilling to provide permission to link study records, medical records, and Medicaid and Vital Records Database records.
- Unwilling to provide informed consent
- Unwilling to be randomized.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- Woman's Hospital — Baton Rouge
Identifiers
NCT: NCT06298214 · RP-23-019