NCT07365579

Brief Summary

This study is testing whether it is feasible to run a larger randomized controlled trial and whether an automated text messaging program is acceptable to young adults who have suicidal thoughts. The program is designed to help participants create and use a safety plan, which is a personalized list of warning signs, coping strategies, supportive people, professional resources, ways to make their environment safer, and reasons for living. After joining and completing an initial survey, participants are randomly assigned by a computer to one of two groups. One group starts right away with the interactive safety planning text program. The other group first receives simple text messages with 24/7 crisis resources and then, after four weeks, also receives the interactive safety planning program. Participants use the text program for about four weeks and complete online surveys at the start and again over a total period of 24 weeks.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
8mo left

Started Apr 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress13%
Apr 2026Jan 2027

First Submitted

Initial submission to the registry

January 22, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

January 26, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

April 1, 2026

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2027

Last Updated

January 27, 2026

Status Verified

January 1, 2026

Enrollment Period

9 months

First QC Date

January 22, 2026

Last Update Submit

January 23, 2026

Conditions

Keywords

Text messagesafety plansuicide prevention

Outcome Measures

Primary Outcomes (3)

  • Frequency of suicidal thoughts

    The number of times an individual has experienced suicidal thoughts

    enrollment to 4 weeks

  • Frequency of suicidal behaviors

    Frequency of suicidal behaviors

    enrollment to 4 weeks

  • Severity of suicidal thoughts

    Severity of suicidal thoughts

    enrollment to 4 weeks

Secondary Outcomes (5)

  • Unbearable Psychache Scale (UP3)

    enrollment to 4 weeks

  • Beck Hopelessness Scale-Short Form (BHS-SF)

    Enrollment to 4 weeks

  • PROMIS Social Isolation - CAT

    Enrollment to 4 weeks

  • Suicide Capacity Scale (SC3)

    enrollment to 4 weeks

  • After-Scenario Questionnaire (ASQ)

    enrollment to 4 weeks

Other Outcomes (1)

  • Suicide Related Coping Scale

    Enrollment to 4 weeks

Study Arms (2)

SMS based safety planning intervention (SMS-SPI)

EXPERIMENTAL

The SMS-SPI consists of a 4-week automated text messaging intervention. It is designed to guide users through the steps of the safety planning process for management of suicide related thoughts and behaviors. The intervention delivers structured, interactive messages daily addressing coping strategies, crisis resources, environmental safety, family and friends for support, distraction techniques, and recognition of warning signs. The number of messages sent each day varies based on users' interactions with the program; users who respond more frequently may receive more messages. In addition to text messaging, the program includes a web-based interface that enabled users to conveniently review and update their safety plan. The SMS-SPI uses message stems that establish a particular topic (e.g., identification of crisis warning signs) and message probes that follow-up on users' responses, which is individualized through branching logic.

Behavioral: Text Messaging based Safety Planning Intervention

Enhanced waitlist control (eWLC)

ACTIVE COMPARATOR

Text messages that are non-interactive and contain referral to crisis services (e.g., the National Suicide Prevention Lifeline, the Crisis Text Line, and (c) the Trevor Project Lifeline). Facilitated referral is a first-line prevention strategy for suicide and is a best-practice commonly integrated into internet-based screenings and informational tools.

Behavioral: Text Messaging based Safety Planning InterventionBehavioral: Facilitated Referral to Crisis Resources

Interventions

Text messages that are non-interactive and contain referral to crisis services (e.g., the National Suicide Prevention Lifeline, the Crisis Text Line, and (c) the Trevor Project Lifeline).

Enhanced waitlist control (eWLC)

A 4-week automated text messaging intervention designed to guide users through the steps of the safety planning process. The intervention delivers structured, interactive messages daily addressing coping strategies, crisis resources, environmental safety, family and friends for support, distraction techniques, and recognition of warning signs.

Enhanced waitlist control (eWLC)SMS based safety planning intervention (SMS-SPI)

Eligibility Criteria

Age18 Years - 24 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Ages 18 to 24 \*The age to provide consent in Nebraska is 19. Individuals recruited from the state of Nebraska must be 19 or older.
  • endorsement of past 2-week suicidal ideation
  • Resident of the United States
  • Owns a smartphone

You may not qualify if:

  • Serious mental illness for which intervention would be contraindicated (i.e., active psychosis or mania)
  • Imminent suicidality (i.e., experiencing active suicidal ideation with a plan and intent to act)
  • Written English language skills that are insufficient to engage in the consent, design, evaluation, or intervention procedures.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Suicidal IdeationBehaviorSuicide Prevention

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral Symptoms

Study Officials

  • Jonah Meyerhoff, PhD

    Northwestern University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
CROSSOVER
Model Details: enhanced waitlist control design
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant Professor

Study Record Dates

First Submitted

January 22, 2026

First Posted

January 26, 2026

Study Start

April 1, 2026

Primary Completion (Estimated)

January 1, 2027

Study Completion (Estimated)

January 1, 2027

Last Updated

January 27, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share