NCT07660133

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2024

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 9, 2026

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2026

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

June 16, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 22, 2026

Completed
Last Updated

June 22, 2026

Status Verified

June 1, 2026

Enrollment Period

1.1 years

First QC Date

June 16, 2026

Last Update Submit

June 16, 2026

Conditions

Keywords

digital mental healthadolescentyouthPublic libraryAnxietycommunity-engagedimplementation

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 COMPARATOR
Behavioral: Library-As-Usual Control Condition

Intervention Condition

EXPERIMENTAL
Behavioral: Technology Enabled Prevention Services

Interventions

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

Also known as: TEPS
Intervention Condition

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

Also known as: Treatment-As-Usual Control Condition
Control Condition

Eligibility Criteria

Age12 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

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

Location

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Ashley A Knapp, MA; PhD

    Northwestern University

    PRINCIPAL INVESTIGATOR

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

Locations