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TEPS for At-Risk Youth

Technology-Enabled Prevention Services for At-Risk Youth

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07660133
Enrollment
66
Registered
2026-06-22
Start date
2024-12-05
Completion date
2026-01-30
Last updated
2026-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Control Condition, Intervention Condition

Keywords

digital mental health, adolescent, youth, Public library, Anxiety, community-engaged, implementation

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.

Interventions

BEHAVIORALTechnology Enabled Prevention Services

Digital mental health intervention focused on anxiety among youth, with one-week and one-month follow-ups

BEHAVIORALLibrary-As-Usual Control Condition

This condition included going over the existing mental health services the library has and then choosing one of those services to participate in

Sponsors

Northwestern University
Lead SponsorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Aged 12-18 years, currently enrolled in high school * Score 5 or above on the GAD-7

Exclusion criteria

* Participated in previous field usability trial

Design outcomes

Primary

MeasureTime frameDescription
AcceptabilityAssessed 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.Program Feedback Questionnaire (PFQ)
Feasibility of Participants Completing the Digital InterventionAssessed at 1-week follow-up (if they started, completed, or did not complete the intervention over the 1 week period). Only intervention condition.Completion of intervention by youth in the intervention condition
UsabilityAssessed 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.System Usability Scale

Secondary

MeasureTime frameDescription
AnxietyAssessed at baseline, one-week follow-up and one-month follow-up for all participantsRCADS-25, anxiety subscale
AvoidanceAssessed at baseline, one-week follow-up and one-month follow-up for all participantsChild-Report Measure of Behavioral Avoidance (CAMS)
Emotion RegulationAssessed at 1-week follow-up (if they started, completed, or did not complete the intervention over the 1 week period). Only intervention condition.Emotion Regulation Questionnaire for Children and Adolescents (ERQ-CA)

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAshley A Knapp, MA; PhD

Northwestern University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 23, 2026