Caring Contacts Via Text Message for Suicidal Adolescents After Emergency Department Discharge

Ann & Robert H Lurie Children's Hospital of Chicago

Status: Not yet enrolling

Conditions: Suicide Prevention

Treatments: Other: Caring Contacts Text Messages

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT07043764

K23MH135206 (U.S. NIH Grant/Contract)

2024-6680

Details and patient eligibility

About

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.

Enrollment: 56 estimated patients

Sex: All

Ages: 12 to 17 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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56 participants in 2 patient groups

Treatment as Usual

No Intervention group

Description:

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.

Caring Contacts

Experimental group

Description:

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

Treatment:

Other: Caring Contacts Text Messages