MedPath

Improving Coping to Reduce Suicide Risk Following ED Discharge

Not Applicable
Not yet recruiting
Conditions
Suicidal
Suicide, Attempted
Suicidal Ideation
Interventions
Behavioral: Electronic Safety Plan (ESP)
Behavioral: Text support
Registration Number
NCT06614946
Lead Sponsor
University of Michigan
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
120
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Enhanced electronic safety plan (ESP) enhanced with 2 reminder text messages with ESP linkElectronic Safety Plan (ESP)-
Electronic safety plan (ESP) + Text-Based SupportElectronic Safety Plan (ESP)Participants who are randomized to this arm will receive ESP during ED care and receive a text-based support program for 4 weeks after discharge, with up to 2 messages per day. The text-based program includes a microrandomized trial (MRT), where participants are randomized twice daily to receive or not receive a message.
Electronic safety plan (ESP) + Text-Based SupportText supportParticipants who are randomized to this arm will receive ESP during ED care and receive a text-based support program for 4 weeks after discharge, with up to 2 messages per day. The text-based program includes a microrandomized trial (MRT), where participants are randomized twice daily to receive or not receive a message.
Primary Outcome Measures
NameTimeMethod
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 months

Measured with a modified Client Satisfaction Questionnaire (CSQ).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Michigan

🇺🇸

Ann Arbor, Michigan, United States

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