Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06456762

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

Led by Vanderbilt University Medical Center · Updated on 2025-11-10

90

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

Sponsors

V

Vanderbilt University Medical Center

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Parents or legal guardians of a child ages 11-17
  • Parents or legal guardians must live with their child 50% of the time
  • Child must be admitted to the pediatric emergency department for a mental health crisis
  • Child must be discharged home from the emergency department with referrals to outpatient care
Not Eligible

You will not qualify if you...

  • Do not have daily access to a mobile phone that can receive SMS text messages
  • Do not speak and read fluently in English

AI-Screening

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Trial Site Locations

Total: 1 location

1

Vanderbilt University Medical Center

Nashville, Tennessee, United States, 37212

Actively Recruiting

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Research Team

M

Margaret Benningfield, MD

CONTACT

N

Neil Chaturvedi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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