Clinical Trial

Design and Feasibility of an SMS-based Safety Planning Intervention

Recruiting
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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.
Protocol Amendment History 3 changes
critical Recruitment opened 2026-06-26
notable Primary completion pushed: 2027-01 -> 2027-05-04 2026-06-26
minor Completion pushed: 2027-01 -> 2027-06-30 2026-06-26
Trial Details
NCT Number NCT07365579
Lead Sponsor Northwestern University
Collaborators: National Institute of Mental Health (NIMH)
Conditions Suicidal Ideation and Behavior
Enrollment 60 participants
Start Date 2026-06-02
Primary Completion 2027-05-04 (estimated)
Study Completion 2027-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-25