Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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: Recruiting NA study of Self Efficacy and Parents, sponsored by Vanderbilt University Medical Center.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
The Child and Adolescent Services Assessment will be used as a parent self-report measure that evaluates the total number of outpatient mental health appointments the participant's child attends during the follow-up period. The outcome will be a total count of the number of outpatient mental health appointments attended.
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2024-08-01 |
| Est. Completion | 2026-12-31 |
| Phase | NA |
What NCT06456762 shows while recruiting
NCT06456762 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 151-participant average among 30 other Self Efficacy trials with a reported enrollment target (40% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Self Efficacy
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 NCT06456762's enrollment target sits among peer trials
90 15th of 30 higher than 15 of 30 other Self Efficacy trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Self Efficacy 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
-
An Informational and Supportive Care Intervention for Patients With Locally Advanced Rectal Cancer
RECRUITING · NA
-
The Fit With Us Study
RECRUITING · NA
-
Health Care Transition Readiness Short-Form Video Intervention
RECRUITING · NA
-
Learning Skills Together Family Caregiver Complex Intervention
RECRUITING · NA
-
Palliative Care Education in Assisted Living for Dementia Care Providers (PCEAL-DCP)
RECRUITING · NA
-
Supervision in Substance Use Disorder Treatment Programs
RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT02521311 · 90 participants · Phase 2
Assessment of Clemastine Fumarate as a Remyelinating Agent in Acute Optic Neuritis (ReCOVER)
- NCT02939573 · 90 participants · Phase 2
A Randomized Multicenter Study for Isolated Skin Vasculitis
- NCT03128879 · 90 participants · Phase 2
Venetoclax With Ibrutinib or Acalabrutinib in Pts. With High-risk CLL
- NCT03184038 · 90 participants · NA
Neurocognition in Patients With Multiple Brain Metastases Treated With Radiosurgery
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI