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Text-based Support for Parents of Adolescents Following an Emergency Department Visits

Effectiveness of Text-based Support for Parents of Suicidal Adolescents Following Emergency Department Visits

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06660199
Acronym
TESP
Enrollment
420
Registered
2024-10-28
Start date
2025-12-01
Completion date
2028-07-31
Last updated
2025-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide

Keywords

Text, Suicidal Ideation, Suicide Attempt

Brief summary

The goal of this study is to determine the effectiveness of an adaptive text-based intervention for parents of adolescents seeking emergency department services for suicide risk concerns.

Detailed description

Participants will be 420 adolescents (ages 13-17) seen in ED with recent suicidal ideation and/or attempt and their parents recruited from two health system EDs in the Midwest.

Interventions

BEHAVIORALText-based intervention

Parents randomized to the texting intervention will receive up to 3 messages each day for 6 weeks: The intervention is comprised of adolescent-centered (A-C) texts focusing on parental adherence to recommended suicide prevention strategies to promote adolescents' safety and parent-centered (P-C) texts focused on improving parents' own well-being.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adolescent (13-17 years old) who present to Emergency Department (ED) due to (1) last-week suicidal ideation and/or (2) last-month suicide attempt, and their caregiver.

Exclusion criteria

Adolescents who are: * medically unstable * presenting with severe cognitive impairment, altered mental status, severe aggression/agitation * presenting without a legal guardian * whose parent does not own a cell phone

Design outcomes

Primary

MeasureTime frameDescription
Aim 1 (primary aim): likelihood of suicidal behavior (actual, interrupted, or aborted attempts)12-week follow-upSuicidal behavior encompasses actual, interrupted, and aborted suicide attempts. Measured with the behavioral subscale of the Columbia-Suicide Severity Rating Scale (C-SSRS),and supplemented with available medical chart data.
Aim 2 (secondary aim) severity of parental stressUp to 6 weeksMeasured with twice daily surveys over the 6-week intervention

Secondary

MeasureTime frameDescription
Aim 1 (primary aim): -time- to- suicidal behavior (actual, interrupted, or aborted suicide attempts24-week follow-upMeasured with the behavioral subscale of C-SSRS and supplemented with available chart data.
Aim 1 (primary aim): time- to- return ED visit24-week follow-up.
Aim 2 (secondary aim): parental negative affectUp to 6 weeksMeasured with twice daily surveys over the 6-week intervention.
Aim 2 (secondary aim) parental positive affectUp to 6 weeksMeasured with twice daily surveys over the 6-week intervention.

Countries

United States

Contacts

Primary ContactEwa Czyz, Ph.D.
ewac@umich.edu734-764-9466

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026