Skip to main content
Clinical Trials/NCT06614946
NCT06614946
Not yet recruiting
Not Applicable

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

University of Michigan1 site in 1 country120 target enrollmentFebruary 1, 2026

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicidal
Sponsor
University of Michigan
Enrollment
120
Locations
1
Primary Endpoint
Percentage of eligible individuals who agree to participate
Status
Not yet recruiting
Last Updated
4 months ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
February 1, 2026
End Date
February 1, 2027
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ewa Czyz

Associate Professor of Psychiatry

University of Michigan

Eligibility Criteria

Inclusion Criteria

  • Individuals presenting to an ED with either:
  • actual, interrupted, or aborted attempt in the last 4 weeks
  • 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

Outcomes

Primary Outcomes

Percentage of eligible individuals who agree to participate

Time Frame: At the time of ED 1 day visit

Completion of the one-month follow-up assessment survey

Time Frame: One month post-discharge from the ED

Completion of the three-month follow-up assessment survey

Time Frame: Three months post-discharge from the ED

Number of withdrawals

Time Frame: Up to 3 months post-discharge from the ED

Percentage of participants who remain active (in text-support condition only)

Time Frame: Up to 28 days post-discharge from the ED

Participant satisfaction with the intervention components

Time Frame: Up to 1 months

Measured with a modified Client Satisfaction Questionnaire (CSQ).

Study Sites (1)

Loading locations...

Similar Trials