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Intervention to Prevent Peer Violence & Depressive Symptoms Among At-Risk Adolescents
NCT03626103 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this investigation is to test the efficacy of "iDOVE2" (a brief emergency department introductory session and longitudinal automated text-message depression prevention program for high-risk teens), and to determine the most potent and parsimonious combination of intervention components for preventing peer violence and depressive symptoms among at-risk youth.
Conditions Studied
Interventions
- BEHAVIORAL + Brief ED Intervention (BI)
- BEHAVIORAL + Text
Study Locations (2)
Connecticut
- Yale New Haven Hospital — New Haven
Rhode Island
- Rhode Island Hospital/Hasbro Children's Hospital — Providence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 800 participants |
| Start Date | 2018-08-01 |
| Est. Completion | 2025-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03626103
The ClinicalTrials.gov registry entry for NCT03626103 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 800 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rhode Island Hospital, which has 110 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Depressive Disorder appearing as the primary indexed condition, and to 2 interventions — of which + Brief ED Intervention (BI) 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: NCT03626103 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Connecticut, Rhode Island. 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 NCT03626103 about?
NCT03626103 is a clinical study titled "Intervention to Prevent Peer Violence & Depressive Symptoms Among At-Risk Adolescents". The purpose of this investigation is to test the efficacy of "iDOVE2" (a brief emergency department introductory session and longitudinal automated text-message depression prevention program for high-risk teens), and to determine the most potent and parsimonious combination of intervention component...
What is the current status of trial NCT03626103?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 800 participants. The study started on 2018-08-01. Estimated completion is 2025-02.
What conditions does trial NCT03626103 study?
This clinical trial studies the following conditions: Depressive Disorder, Violence. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03626103?
The interventions under investigation include: + Brief ED Intervention (BI) (BEHAVIORAL), + Text (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03626103?
This trial is sponsored by Rhode Island Hospital, which has 110 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03626103 being conducted?
This trial has 2 study locations across Connecticut, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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