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NCT06133829 · ClinicalTrials.gov registry record · NA
upREACH Perinatal Home Visitation Program
A NA study of Pregnancy and Postpartum, sponsored by Baylor College of Medicine.
- Active
- Registry status
- NA
- Development phase
- 450
- Enrollment target
- 1
- Study location
NCT06133829 is a NA study of Pregnancy and Postpartum that is active but no longer recruiting, run by Baylor College of Medicine. The registered enrollment target is 450 participants, below the 870-participant average among 191 other Pregnancy trials with a reported enrollment target (48% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06133829, a NA study of Pregnancy and Postpartum, is active but no longer recruiting, sponsored by Baylor College of Medicine.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 450 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess the effectiveness of a new brief home visitation program delivered by non-nurse home visitors to 1) improve connections to community resources based on reported and assessed needs, 2) increase health self-efficacy, and 3) reduce maternal stress compared to a control group that receives standard care from an obstetric clinic. Secondary administrative data on infant birth outcomes, health care use during the first year of life (appointment adherence), and interaction with government services (such as public assistance or child welfare) will be compared between the groups. For the intervention group, we will secondarily also assess home visit compliance and satisfaction with the intervention. Participants will be asked to complete questionnaires that include questions about the participant, their pregnancy, their feelings, their family, and their use of social/community services. Half of the women in this study will be randomly offered free home visitation services and the other half of women in this study will receive standard services from the clinic. The intervention group will be offered at least two free home visits with a non-nurse home visitor. During these visits, the home visitor will provide them with resources and tools to help the participant prepare for their baby. All participants will complete a second round of electronic surveys at approximately 2 months postpartum. Intervention participant outcomes will be compared to a control group that receive standard care from an obstetric clinic.
Conditions Studied
Interventions
- BEHAVIORAL upREACH Home Visitation Program
Study Locations (1)
Texas
- Harris Health/Baylor College of Medicine - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 450 participants |
| Start Date | 2024-01-22 |
| Est. Completion | 2026-11-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06133829
The ClinicalTrials.gov registry entry for NCT06133829 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 450 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 870-participant average among 191 other Pregnancy trials with a reported enrollment target (48% lower). The listed sponsor is Baylor College of Medicine, which has 616 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 1 intervention - of which upREACH Home Visitation Program is the first listed.
NCT06133829 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT06133829 about?
NCT06133829 is a clinical study titled "upREACH Perinatal Home Visitation Program". The purpose of this study is to assess the effectiveness of a new brief home visitation program delivered by non-nurse home visitors to 1) improve connections to community resources based on reported and assessed needs, 2) increase health self-efficacy, and 3) reduce maternal stress compared to a co...
What is the current status of trial NCT06133829?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 450 participants. The study started on 2024-01-22. Estimated completion is 2026-11-30.
What conditions does trial NCT06133829 study?
This clinical trial studies the following conditions: Pregnancy, Postpartum.
What interventions are being tested in trial NCT06133829?
The interventions under investigation include: upREACH Home Visitation Program (BEHAVIORAL).
Who is sponsoring clinical trial NCT06133829?
This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06133829 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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