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Recruiting NCT06614946

NCT06614946 Improving Coping to Reduce Suicide Risk Following ED Discharge

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Clinical Trial Summary
NCT ID NCT06614946
Status Recruiting
Phase
Sponsor University of Michigan
Condition Suicidal
Study Type INTERVENTIONAL
Enrollment 120 participants
Start Date 2026-05-12
Primary Completion 2027-02

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 65 Years
Study Type INTERVENTIONAL
Interventions
Electronic Safety Plan (ESP)Text support

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 120 participants in total. It began in 2026-05-12 with a primary completion date of 2027-02.

⚠ 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 researchers hope to learn whether an electronic safety plan (ESP) and a supportive text messaging program are feasible and acceptable to adult patients with recent suicidal thoughts or behavior after emergency department (ED) discharge. From this study, the researchers also hope to learn how to best carry out the ESP and text messaging program to improve outcomes for patients after ED discharge.

Eligibility Criteria

Inclusion Criteria: Individuals presenting to an ED with either: 1. actual, interrupted, or aborted attempt in the last 4 weeks 2. suicidal ideation within the last week Exclusion Criteria: * Severe cognitive impairment or altered mental status (psychosis, manic state) * Severe aggression/agitation, * Being admitted or transferred into inpatient care, * Patient not owning a cell phone with text messaging capability

Contact & Investigator

Central Contact

Ewa Czyz

✉ ewac@umich.edu

📞 734-764-9466

Principal Investigator

Ewa Czyz, Ph.D.

PRINCIPAL INVESTIGATOR

University of Michigan

Frequently Asked Questions

Who can join the NCT06614946 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Suicidal. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06614946 currently recruiting?

Yes, NCT06614946 is actively recruiting participants. Contact the research team at ewac@umich.edu for enrollment information.

Where is the NCT06614946 trial being conducted?

This trial is being conducted at Ann Arbor, United States.

Who is sponsoring the NCT06614946 clinical trial?

NCT06614946 is sponsored by University of Michigan. The principal investigator is Ewa Czyz, Ph.D. at University of Michigan. The trial plans to enroll 120 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology