13 and older, any sex, with Suicide. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Percentage of Eligible Youth-Parent Dyads Who Agree to Participate in the Study,Primary· At the time of youth Emergency Department visit
Data represent participant dyads who were eligible and approached about study participation, and who agreed to take part in the study.
Group
Value
95% CI
Participants Consented
125
Participant Dyads Who Completed Follow-up AssessmentsPrimary· Up to 12 weeks
Data was used to determine retention rate among the participant dyads. We report on follow up completion for both adolescent and caregiver members of the dyad.
Count of Parent responses
Group
Value
95% CI
Control
33
A-F Texting Component
42
A-F Texting Plus P-F Texting Component
38
Count of Adolescent Responses
Group
Value
95% CI
Control
29
A-F Texting Component
35
A-F Texting Plus P-F Texting Component
27
Percentage of Participants Randomized to the Intervention Who Remained Active (Texting Arms Only)Primary· Up to 6 weeks
Results represent parent participants who did not request stopping the intervention (i.e., did not request to stop receiving messages).
Group
Value
95% CI
A-F Texting Component
42
A-F Texting Plus P-F Texting Component
39
Participating Parents' Satisfaction With the Intervention (Texting Arms Only)Primary· Up to 6 weeks
Measured using the Modified Client Satisfaction Questionnaire (CSQ), which was a 2-question survey. Each question had a range of 1-4. Adult participants were asked to rate both their overall satisfaction (1 meaning not satisfied to 4 meaning highly satisfied), and the likelihood that they would recommend their particular assigned intervention to a friend (1 meaning highly unlikely to 4 meaning highly likely).
Overall satisfaction
Group
Value
95% CI
A-F Texting Component
3.51
± 0.56
A-F Texting Plus P-F Texting Component
3.37
± 0.60
Recommend to a friend
Group
Value
95% CI
A-F Texting Component
3.56
± 0.55
A-F Texting Plus P-F Texting Component
3.43
± 0.66
Number of and Reasons for Active WithdrawalsPrimary· Up to 12 weeks
Parent participant request to withdraw from the study. Study intention was to collect the number of and reasons for withdrawals, but the sole withdrawal did not provide a reason.
Group
Value
95% CI
Control
0
A-F Texting Component
0
A-F Texting Plus P-F Texting Component
1
Adverse events — posted to ClinicalTrials.gov
Time frame: Up to 12 weeks.
Reporting threshold: 5%.
Adverse-event reports describe events observed during the trial — not all are caused by the drug.
The researchers seek to develop a text message intervention for caregivers of adolescents at elevated suicide risk following discharge from emergency department (ED) care.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
NCT07404787 — Evaluation of a Telehealth Case Management Intervention to Prevent Suicide Among Soldiers Discharged From Psychiatric Ho
· NA
· recruiting
NCT07214233 — Youth Empowerment and Safety Intervention
· NA
· recruiting
NCT07343258 — Pilot Study on Follow-Up of (Acutely) Suicidal Individuals From the Flemish Suicide Helpline
· NA
· recruiting
NCT07523490 — Investigation on Suicide Risk Factors of Patients With Mood Disorders
· recruiting
NCT06571916 — Brief Skills for Safer Living (Brief-SfSL)
· NA
· recruiting
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by University of Michigan
Last refreshed: 16 May 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05058664.