TEPS for At-Risk Youth
Technology-Enabled Prevention Services for At-Risk Youth
2 other identifiers
interventional
66
1 country
1
Brief Summary
The goal of this aim was to conduct a randomized pilot trial evaluating the feasibility and acceptability of the co-created digital mental health program for anxiety among youth with elevated anxiety. Youth were recruited from local public libraries, and the program was integrated into the teen programming of library services.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 5, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 9, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2026
CompletedFirst Submitted
Initial submission to the registry
June 16, 2026
CompletedFirst Posted
Study publicly available on registry
June 22, 2026
CompletedJune 22, 2026
June 1, 2026
1.1 years
June 16, 2026
June 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Acceptability
Program Feedback Questionnaire (PFQ)
Assessed at the time the online intervention was taken during the 1-week period between baseline and the 1-week follow-up. Only for intervention condition.
Feasibility of Participants Completing the Digital Intervention
Completion of intervention by youth in the intervention condition
Assessed at 1-week follow-up (if they started, completed, or did not complete the intervention over the 1 week period). Only intervention condition.
Usability
System Usability Scale
Assessed at the time the online intervention was taken during the 1-week period between baseline and the 1-week follow-up. Only for intervention condition.
Secondary Outcomes (3)
Anxiety
Assessed at baseline, one-week follow-up and one-month follow-up for all participants
Avoidance
Assessed at baseline, one-week follow-up and one-month follow-up for all participants
Emotion Regulation
Assessed at 1-week follow-up (if they started, completed, or did not complete the intervention over the 1 week period). Only intervention condition.
Study Arms (2)
Control Condition
ACTIVE COMPARATORIntervention Condition
EXPERIMENTALInterventions
Digital mental health intervention focused on anxiety among youth, with one-week and one-month follow-ups
This condition included going over the existing mental health services the library has and then choosing one of those services to participate in
Eligibility Criteria
You may qualify if:
- Aged 12-18 years, currently enrolled in high school
- Score 5 or above on the GAD-7
You may not qualify if:
- Participated in previous field usability trial
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Northwestern University, Feinberg School of Medicine
Chicago, Illinois, 60611, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ashley A Knapp, MA; PhD
Northwestern University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
June 16, 2026
First Posted
June 22, 2026
Study Start
December 5, 2024
Primary Completion
January 9, 2026
Study Completion
January 30, 2026
Last Updated
June 22, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share