NCT07411300 Supporting Caregivers Following Mental Health Emergency Department Visits
| NCT ID | NCT07411300 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ann & Robert H Lurie Children's Hospital of Chicago |
| Condition | Caregiver Participation |
| Study Type | INTERVENTIONAL |
| Enrollment | 75 participants |
| Start Date | 2026-01-26 |
| Primary Completion | 2026-08-31 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 75 participants in total. It began in 2026-01-26 with a primary completion date of 2026-08-31.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The investigators plan to conduct a pilot hybrid effectiveness-implementation type 1 randomized controlled trial comparing 3 arms of varying follow-up intervention. Caregivers of youth ages 10-17 who present to the Lurie Children's Hospital ED with suicidal thoughts or behaviors (STBs) and are discharged with a safety plan will be included in the current study. Families will be randomized to receive either 1) treatment as usual, 2) follow-up phone calls, or 3) automatic electronic medical record (EMR) MyChart messages
Eligibility Criteria
Inclusion Criteria: * Participants are eligible for participation in the current study if they are parent/guardians of youth ages 10-17 who received a psychiatric evaluation in the ED for suicidal thoughts or behaviors and are being discharged with a safety plan Exclusion Criteria: * Parents/guardians will be excluded from recruitment if the youth is in state custody, if they are not proficient in English or Spanish, if the patient is being admitted or transferred for medical or psychiatric hospital admission, or they are not willing to enroll in MyChart through the EMR. The investigators are also only enrolling one caregiver per patient. In other words, if a patient returns to the ED with a different caregiver, the investigators will not enroll the other caregiver.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07411300 clinical trial?
This trial is open to participants of all sexes, aged 10 Years or older, up to 17 Years, studying Caregiver Participation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07411300 currently recruiting?
Yes, NCT07411300 is actively recruiting participants. Contact the research team at aburnside@luriechildrens.org for enrollment information.
Where is the NCT07411300 trial being conducted?
This trial is being conducted at Chicago, United States.
Who is sponsoring the NCT07411300 clinical trial?
NCT07411300 is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago. The trial plans to enroll 75 participants.