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Improving Coping to Reduce Suicide Risk Following ED Discharge

Facilitating Effective Coping to Reduce Suicide Risk Following ED Discharge: A Micro-randomized Trial to Develop an Adaptive Text-based Intervention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06614946
Enrollment
120
Registered
2024-09-26
Start date
2026-05-12
Completion date
2027-02-01
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicidal, Suicidal Ideation, Suicide, Attempted

Keywords

Emergency Department

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.

Interventions

BEHAVIORALElectronic Safety Plan (ESP)

Participants will receive an electronic safety plan in the ED. ESP focuses on developing a personalized coping plan to manage suicidal thoughts and urges.

BEHAVIORALText support

Those in the text-based support program will receive up to 2 texts per day for a month with varying levels of tailoring, based on ESP and dynamic personalized feedback.

Sponsors

University of Michigan
Lead SponsorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

There are 2 arms: ESP only and ESP with text-based program. The ESP with text-based program arm includes twice daily (within-person) randomizations.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Percentage of eligible individuals who agree to participateAt the time of ED 1 day visit
Completion of the one-month follow-up assessment surveyOne month post-discharge from the ED
Completion of the three-month follow-up assessment surveyThree months post-discharge from the ED
Number of withdrawalsUp to 3 months post-discharge from the ED
Percentage of participants who remain active (in text-support condition only)Up to 28 days post-discharge from the ED
Participant satisfaction with the intervention componentsUp to 1 monthsMeasured with a modified Client Satisfaction Questionnaire (CSQ).

Countries

United States

Contacts

CONTACTEwa Czyz
ewac@umich.edu734-764-9466
PRINCIPAL_INVESTIGATOREwa Czyz, Ph.D.

University of Michigan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026