Caring Contacts Via Text Message for Suicidal Adolescents After Emergency Department Discharge
Caring Texts for Adolescents to Reduce Suicide Risk
2 other identifiers
interventional
56
1 country
1
Brief Summary
The goal of this pilot clinical trial is to learn if Caring Contacts (brief, hopeful, supportive text messages) can be delivered to adolescents with suicidal thoughts or behaviors after discharge from the emergency department, and to understand if adolescents find it acceptable to receive Caring Contacts. Researchers will also begin to explore how suicidal thoughts and behaviors change over time among participants who receive Caring Contacts along with treatment as usual, compared to participants who only receive treatment as usual. All participants will be invited to answer survey questions when they first enroll in the study and 1, 3, 6, and 12 months after their emergency department visit. Some participants will receive Caring Contacts (brief, hopeful, supportive text messages) after their emergency department visit. Some participants will be invited to complete an interview about their experiences receiving Caring Contacts.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2025
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 20, 2025
CompletedFirst Posted
Study publicly available on registry
June 29, 2025
CompletedStudy Start
First participant enrolled
December 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2028
June 29, 2025
June 1, 2025
2.7 years
June 20, 2025
June 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Columbia-Suicide Severity Rating Scale (C-SSRS) Self-Report Recent
The Columbia-Suicide Severity Rating Scale (C-SSRS) Self-Report Recent measures recent suicidal ideation and behavior on a scale of 0-5, with higher scores indicating greater severity.
Baseline, 1 Month, 3 Months, 6 Months, 12 Months
Study Arms (2)
Treatment as Usual
NO INTERVENTIONTreatment as usual consists of a suicide risk assessment during the emergency department visit, determination of disposition, safety planning, provision of crisis resources, and coordination of follow-up mental health services if indicated.
Caring Contacts
EXPERIMENTALIn addition to Treatment as Usual, participants will receive Caring Contacts, consisting of brief, hopeful, supportive text messages.
Interventions
Caring Contacts are brief, hopeful, supportive text messages.
Eligibility Criteria
You may qualify if:
- to \<18 years of age
- Present to the emergency department with suicidal thoughts or behaviors as indicated by the Ask Suicide-Screening Questions (ASQ)
- Have a cell phone that can receive text messages
- Proficient in English
- Anticipated disposition of discharge from the emergency department
You may not qualify if:
- In care of the Department of Children and Family Services
- Unable to participate meaningfully in assent, assessments, or the intervention, as determined by the treating clinician, including any of the following: acute or chronic cognitive impairment, acute psychosis, current severe agitation, current alcohol or drug intoxication
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, Illinois, 60611, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jennifer A. Hoffmann, MD, MS
Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor of Pediatrics
Study Record Dates
First Submitted
June 20, 2025
First Posted
June 29, 2025
Study Start
December 1, 2025
Primary Completion (Estimated)
August 1, 2028
Study Completion (Estimated)
August 1, 2028
Last Updated
June 29, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- Data will be made available 1 year after completion of the study
- Access Criteria
- Approval by NIMH Data Archive
Data will be shared through the NIMH Data Archive