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ACTIVE NOT RECRUITING NA

Reducing Racism and Discrimination in Schools: Comprehensive Prevention Services

NCT05189769 · View on ClinicalTrials.gov ↗

Study Summary

The primary purpose of this project is to test a comprehensive, two-part intervention with ReACT and a recently adapted, Coping Power+ Program. ReACT and PBIS are school-wide universal interventions. Coping Power and Coping Power+ are targeted preventive interventions designed to assist at-risk 7th grade students to improve their coping with interpersonal stressors during middle school. This project will evaluate the effects of the program on teacher, student and parent perceptions of school climate, student behavior, social-emotional competence, disciplinary infractions, and identity for 7th grade students in Coping Power or Coping Power+

Conditions Studied

Interventions

  • BEHAVIORAL CP no REACT
  • BEHAVIORAL CP+/No REACT
  • BEHAVIORAL CP and REACT
  • BEHAVIORAL CP+ and REACT

Study Locations (2)

Alabama

  • Jefferson County Public Schools — Birmingham
  • Huntsville City Schools — Huntsville

Trial Details

FieldValue
Enrollment Target 1,093 participants
Start Date 2019-05-15
Est. Completion 2025-12-01
Phase NA

Sponsor

University of Alabama, Tuscaloo

76 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05189769

The ClinicalTrials.gov registry entry for NCT05189769 describes a study currently listed as active not 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 1,093 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Alabama, Tuscaloo, which has 76 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Behavior, Child appearing as the primary indexed condition, and to 4 interventions — of which CP no REACT 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: NCT05189769 reports 2 study locations spanning 1 distinct geographic area — top geographies include Alabama. 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 NCT05189769 about?

NCT05189769 is a clinical study titled "Reducing Racism and Discrimination in Schools: Comprehensive Prevention Services". The primary purpose of this project is to test a comprehensive, two-part intervention with ReACT and a recently adapted, Coping Power+ Program. ReACT and PBIS are school-wide universal interventions. Coping Power and Coping Power+ are targeted preventive interventions designed to assist at-risk 7th ...

What is the current status of trial NCT05189769?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 1,093 participants. The study started on 2019-05-15. Estimated completion is 2025-12-01.

What conditions does trial NCT05189769 study?

This clinical trial studies the following conditions: Behavior, Child. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05189769?

The interventions under investigation include: CP no REACT (BEHAVIORAL), CP+/No REACT (BEHAVIORAL), CP and REACT (BEHAVIORAL), CP+ and REACT (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05189769?

This trial is sponsored by University of Alabama, Tuscaloo, which has 76 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05189769 being conducted?

This trial has 2 study locations across Alabama. 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