PES Family Support and Follow-Up Program

NCT03655119 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 229

Last updated 2022-04-14

No results posted yet for this study

Summary

The Psychiatric Emergency Services (PES) Family Support and Follow-Up Program is a service delivery intervention that utilizes a multi-component approach to enhance usual care provided to youth and families at the University of Michigan Psychiatric Emergency Services in order to promote youth safety and provide support to families following their visit. During the first phase of intervention, families will receive enhanced usual care by clinical staff along with a family toolkit that includes a youth safety plan and written recommendations for safety monitoring and supporting youth during a crisis. During the second phase of intervention, families will receive the interventions provided during the first phase in addition to caring contacts post discharge, which may occur by phone, text, or email. Caring contacts are meant to provide support, additional education, and problem solving assistance.

Conditions

  • Suicide

Interventions

BEHAVIORAL

Parent toolkit

The parent tookit is a resource that reinforces evidence-based practices for crisis management such as safety planning and means restriction and encourages parents to increase their support, supervision, and monitoring of their at risk youth.

BEHAVIORAL

Enhanced Care

PES clinical staff will receive training on the best practices in brief crisis-focused interventions in emergency settings with parents and youth.

BEHAVIORAL

Caring Follow-Up Messages

Parents will receive caring contacts via phone, text, or email to provide support, additional education, and problem solving assistance in the days and weeks post-discharge.

Sponsors & Collaborators

  • Michigan Department of Health and Human Services

    collaborator OTHER
  • Substance Abuse and Mental Health Services Administration (SAMHSA)

    collaborator FED
  • University of Michigan

    lead OTHER

Principal Investigators

  • Cynthia Ewell Foster, Ph.D. · University of Michigan

  • Patricia Smith, MA · Michigan Department of Health and Human Services

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
10 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-10
Primary Completion
2020-03-11
Completion
2020-03-11

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03655119 on ClinicalTrials.gov