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RECRUITING NA

Optimizing a Digital AEP Risk Intervention With Native Women and Communities

NCT06324929 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of Aim 1 of the study is to gather quantitative and qualitative information to inform the development of a digital app tailored for Native American women to help them avoid a pregnancy affected by alcohol. In Aim 2, we will Pilot test 5 new candidate components tailored to Native women at risk of AEP

Interventions

  • BEHAVIORAL CARRII Native Rapid Pilot Testing

Study Locations (1)

Virginia

  • University of Virginia Fontaine Research Park — Charlottesville

Trial Details

FieldValue
Enrollment Target 350 participants
Start Date 2024-05-16
Est. Completion 2025-10-17
Phase NA

Sponsor

University of Virginia

392 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06324929

The ClinicalTrials.gov registry entry for NCT06324929 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 350 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Virginia, which has 392 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Sexual Behavior appearing as the primary indexed condition, and to 1 intervention — of which CARRII Native Rapid Pilot Testing is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06324929 reports 1 study location spanning 1 distinct geographic area — top geographies include Virginia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06324929 about?

NCT06324929 is a clinical study titled "Optimizing a Digital AEP Risk Intervention With Native Women and Communities". The purpose of Aim 1 of the study is to gather quantitative and qualitative information to inform the development of a digital app tailored for Native American women to help them avoid a pregnancy affected by alcohol. In Aim 2, we will Pilot test 5 new candidate components tailored to Native women a...

What is the current status of trial NCT06324929?

This trial is currently recruiting. It is a NA study. The enrollment target is 350 participants. The study started on 2024-05-16. Estimated completion is 2025-10-17.

What conditions does trial NCT06324929 study?

This clinical trial studies the following conditions: Sexual Behavior, Alcohol Use, Unspecified, Unplanned Pregnancy, Alcohol Exposed Pregnancy, Contraception Use. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06324929?

The interventions under investigation include: CARRII Native Rapid Pilot Testing (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06324929?

This trial is sponsored by University of Virginia, which has 392 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06324929 being conducted?

This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial