Mode
Text Size
Log in / Sign up
N/A N=120 Randomized Single-blind Supportive Care

Developing Text-based Support for Parents of Adolescents After an Emergency Department Visit

Suicide

Enrolled (actual)
120
Serious AEs
11.4%
Results posted
May 2024
Primary outcome: Primary: Percentage of Eligible Youth-Parent Dyads Who Agree to Participate in the Study, — 125 Parent-youth dyads

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
A-F texting component (Behavioral); P-F texting component (Behavioral)
Age
Pediatric, Adult, Older Adult · 13+ yrs
Sex
All
Sponsor
University of Michigan
Primary completion
Sep 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Eligible Youth-Parent Dyads Who Agree to Participate in the Study,
125
PRIMARY
Participant Dyads Who Completed Follow-up Assessments
33; 42; 38; 29; 35; 27
PRIMARY
Percentage of Participants Randomized to the Intervention Who Remained Active (Texting Arms Only)
42; 39
PRIMARY
Participating Parents' Satisfaction With the Intervention (Texting Arms Only)
3.51; 3.37; 3.56; 3.43
PRIMARY
Number of and Reasons for Active Withdrawals
0; 0; 1

Summary

The researchers seek to develop a text message intervention for caregivers of adolescents at elevated suicide risk following discharge from emergency department (ED) care.

Eligibility Criteria

Parent eligibility:

Inclusion Criteria

  • Parent of eligible teen

Exclusion Criteria

  • Not owning a cell phone with text messaging capability.

Teen eligibility:

Inclusion Criteria

  • Recent suicidal ideation (within last 2 weeks) and/or suicide attempt within the last month.

Exclusion Criteria

  • Youth with severe cognitive impairment or altered mental status (e.g., psychosis, manic state)
  • Youth with severe aggression/agitation
  • No availability of a legal guardian
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05058664). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search