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Clinical Trials/NCT07043764
NCT07043764RecruitingNot Applicable

Caring Texts for Adolescents to Reduce Suicide Risk

Ann & Robert H Lurie Children's Hospital of Chicago1 site in 1 country56 target enrollmentStarted: September 15, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
56
Locations
1
Primary Endpoint
Columbia-Suicide Severity Rating Scale (C-SSRS) Self-Report Recent

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
12 Years to 17 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •12 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

Exclusion Criteria

  • •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

Arms & Interventions

Caring Contacts

Experimental

In addition to Treatment as Usual, participants will receive Caring Contacts, consisting of brief, hopeful, supportive text messages.

Intervention: Caring Contacts Text Messages (Other)

Treatment as Usual

No Intervention

Treatment 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.

Outcomes

Primary Outcomes

Columbia-Suicide Severity Rating Scale (C-SSRS) Self-Report Recent

Time Frame: Baseline, 1 Month, 3 Months, 6 Months, 12 Months

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.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jennifer Hoffmann

Associate Professor of Pediatrics

Ann & Robert H Lurie Children's Hospital of Chicago

Study Sites (1)

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