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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: Active NA study of Pregnancy and Postpartum, sponsored by Baylor College of Medicine.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Measured by Family Resource Scale (higher score shows that resources are more adequate)
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 |
What the registry record for NCT06133829 still lists
NCT06133829 is an interventional study that assigns participants to a tested intervention. The registered 450 participants enrollment target is mid-sized for trials with a published cap, below the 870-participant average among 191 other Pregnancy trials with a reported enrollment target (48% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Pregnancy
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06133829's enrollment target sits among peer trials
450 54th of 191 higher than 137 of 191 other Pregnancy trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pregnancy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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