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NCT06456762 · ClinicalTrials.gov registry record · NA

Text-messaging Intervention to Support Parents After Their Child's Psychiatric Emergency

A NA study of Self Efficacy and Parents, sponsored by Vanderbilt University Medical Center.

Recruiting
Registry status
NA
Development phase
90
Enrollment target
1
Study location

NCT06456762 is a NA study of Self Efficacy and Parents that is actively recruiting participants, run by Vanderbilt University Medical Center. The registered enrollment target is 90 participants, below the 151-participant average among 30 other Self Efficacy trials with a reported enrollment target (40% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06456762, a NA study of Self Efficacy and Parents, is actively recruiting participants, sponsored by Vanderbilt University Medical Center.

RECRUITING
Registry status
NA
Development phase
90 participants
Enrollment target
1
Study location

Study Summary

This grant aims to develop and test a text-messaging intervention for parents of children and teens evaluated in the emergency department for a psychiatric emergency and discharged home with outpatient referrals. The intervention for parents will teach parents skills to navigate the mental health services system and build their self-efficacy in managing their child's mental health. This research has the potential to improve services for families seeking emergency psychiatric support, with the goal of facilitating treatment engagement and reducing emergency services utilization using scalable, cost-effective, accessible tools.

Interventions

  • BEHAVIORAL iPEACE: Intervention for Parent Education about Care after the ED
  • BEHAVIORAL Text Messaging Reminders Only

Study Locations (1)

Tennessee

  • Vanderbilt University Medical Center - Nashville

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2024-08-01
Est. Completion 2026-12-31
Phase NA

What the Registry Record Tells You About NCT06456762

The ClinicalTrials.gov registry entry for NCT06456762 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 151-participant average among 30 other Self Efficacy trials with a reported enrollment target (40% lower). The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Self Efficacy appearing as the primary indexed condition, and to 2 interventions - of which iPEACE: Intervention for Parent Education about Care after the ED is the first listed.

NCT06456762 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.

Frequently Asked Questions

What is clinical trial NCT06456762 about?

NCT06456762 is a clinical study titled "Text-messaging Intervention to Support Parents After Their Child's Psychiatric Emergency". This grant aims to develop and test a text-messaging intervention for parents of children and teens evaluated in the emergency department for a psychiatric emergency and discharged home with outpatient referrals. The intervention for parents will teach parents skills to navigate the mental health se...

What is the current status of trial NCT06456762?

This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2024-08-01. Estimated completion is 2026-12-31.

What conditions does trial NCT06456762 study?

This clinical trial studies the following conditions: Self Efficacy, Parents, Mental Health Literacy, Psychiatric Emergency.

What interventions are being tested in trial NCT06456762?

The interventions under investigation include: iPEACE: Intervention for Parent Education about Care after the ED (BEHAVIORAL), Text Messaging Reminders Only (BEHAVIORAL).

Who is sponsoring clinical trial NCT06456762?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06456762 being conducted?

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

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.