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NCT Number: NCT07539636

Virtual Intervention for Behavioral Health in Emerging Adults; "VIBE in the Parks"

The goal of this study is first to develop and adapt a digital low-intensity treatment, "VIBE in the Parks", for adolescents and young adults (AYA) who visit programming at the Chicago Park District. A trial will occur at four Park District sites to compare how "VIBE in the Parks" works compared to a control condition (where AYA are given access to a digital workbook).

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Key information

Age range

13 year–24 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Amid an unprecedented youth mental health crisis, adolescents and young adults (AYA) have the most barriers to receiving mental healthcare. While digital tools are a scalable and accessible way to provide timely mental health screening and referral options, these tools have failed to engage AYA in their daily lives. This failure is driven by multiple factors, including a lack of: 1) understanding of implementation determinants for digital tools in community spaces; and 2) partnership with AYA, their caregivers, and support staff who work in key community settings where AYA spend their time. The goal of this study is to target AYA engagement in the design and implementation of a digital low-intensity treatment for AYA in Chicago Park District (CPkD) Teen Programming. The CPkD is the largest park district in the country, and more than 40,000 youth are served daily across all 77 Chicago neighborhoods. This project harnesses on a partnership with CPkD and is grounded in the Accelerated Creation-to-Sustainment (ACTS) Model to guide the development of a technology ("VIBE in the Parks"), as well as its service and implementation plans for CPkD sites. Aim 1 follows the first phase of the ACTS Model, Create. Human-centered design and community-engaged research methodologies will be used to collaborate with the existing CPkD Youth Advisory Board and Teen Programming participants, caregivers of AYA served by CPkD, and CPkD staff. Design activities will focus on targeting mechanisms that are believed to influence engagement: 1) individual-level barriers to care; 2) leveraging spaces where youth spend their time, including assessing determinants in these spaces; and 3) elevating key player input throughout design. The products of Aim 1 will include: an initial version of "VIBE in the Parks" that demonstrates usability and acceptability by key players, a service protocol for integration of the "VIBE in the Parks" and potential higher clinical needs reported by AYA as a result of using the tool, and an implementation blueprint for integration into CPkD programming. Additionally, extended usability testing will pilot all trial activities to be conducted in Aim 2. In Aim 2, the second phase of the ACTS Model, Trial, will be followed by conducting a pilot randomized controlled trial in CPkD sites using an Optimization, Effectiveness, and Implementation trial methodology. The "VIBE in the Parks" will be compared to a control condition (digital workbook) across a pragmatic, rollout implementation trial. Primary outcomes include acceptability and feasibility, along with reductions of individual levels to mental healthcare, DMH use, and, secondarily, clinical outcomes (anxiety, depression). Optimization activities will occur across the trial period. In sum, the naturalistic approach of this work addresses multiple barriers to real-world digital tool engagement failures for AYA. It will provide key insights into engagement strategies, adaptations, and both service and implementation practices that will support AYA in community settings.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be a participant in Chicago Park District Teen Programming at a trial site
  • Be between the ages of 13-24 years of age
  • Be able to speak and read in English

Exclusion criteria

  • Absence of the above criteria

Treatment and study plan

"VIBE in the Parks"

Behavioral

"VIBE in the Parks" will be developed across Aim 1 activities and will include screening, feedback, and access to digital resources related to symptoms

Digital Control

Behavioral

Digital control will include providing participants access to a digital workbook for Cognitive Behavioral Therapy (CBT)

Primary outcomes

  1. After Scenario Questionnaire

    Time frame: Administered three times; baseline, week 2, week 4

    3-items; 7-point scale (i.e., 1-7), with higher scores indicating greater satisfaction; Assesses satisfaction

  2. Kiddie Computerized Adaptive Tests, Anxiety and Depression Modules

    Time frame: Administered five times; baseline and at weeks 1, 2, 3, and 4

    ~1 minute to complete each self-report module, assess anxiety and depressive symptoms; Higher scores indicate greater symptom severity

  3. TeACH System Individual Barriers and Engagement Questionnaire

    Time frame: Administered 5 times, at baseline and weeks 1, 2, 3, 4

    4-items; Mental Health Understanding, Confidence to Act, Likelihood to use DMH (5-point Likert Scale, higher scores indicate greater understanding, confidence, likelihood); DMH Use (Y/N/Unsure)

  4. Twente Engagement with Ehealth Technologies Scale

    Time frame: Administered five times, at baseline and weeks 1, 2, 3, 4

    9-items on a 5-point scale, with higher scores indicating stronger engagement; Engagement with e-health (behavior, cognition, affect)

Secondary outcomes

  1. Generalized Anxiety Disorder-7

    Time frame: Administered twice, at baseline and week 4

    7-items, 4-point scale (i.e., 0-3), with higher scores indicating more anxiety symptoms; Anxiety; Administered to ages 18+

  2. Patient Health Questionnaire-9

    Time frame: Administered twice, at baseline and week 4

    9-items, 4-point scale (i.e., 0-3), with higher scores indicating more depressive symptoms; Depression; Administered to ages 18+

  3. Revised Children's Anxiety and Depression Scale

    Time frame: Administered twice, at baseline and week 4

    25-items, 4-point scale (i.e., 0-3), with higher scores indicating more symptoms; Anxiety, Low Mood; Administered to ages 13-17, Parents when opted in

  4. Mental Health Implementation Science Tools - Consumer Version

    Time frame: Administered three times, at baseline, weeks 2 and 4

    Assess mental health interventions by implementation domains on a 7-point Likert Scale, with higher scores indicating stronger agreement; subscales administered: Acceptability, Appropriateness, Accessibility/Reach

  5. Self-Stigma of Seeking Help Scale

    Time frame: Administered three times, at baseline, weeks 2 and 4

    10-items, 5-point scale (i.e., 1-5), with higher scores indicating more agreement; feelings of stigma around receiving mental health care

Other outcomes

  1. WHO Disability Assessment Schedule 2.0

    Time frame: Administered once, at baseline

    12-Items, 5-point scale (i.e., 0-4), with higher scores indicating more severity; health and disability; Administered to ages 18+

  2. DSM-5 Cross-Cutting Symptom Measure

    Time frame: Administered once, at baseline

    23 item (adult) or 25 item (child) self-report tool using a 5-point scale (i.e., 0-4), with scores reviewed by domain and not as a total sum; Assesses mental health

Sponsors and collaborators

Lead sponsor

University of Illinois at Chicago

Other

Registry information

Official study title

Reaching Teens Where They Are: Integrating Digital Low-Intensity Mental Health Treatment Into Park District Teen Programming

Acronym: VIBE

Important dates

Study start
2027
Primary completion
2028
Study completion
2028
First posted
Apr 20, 2026
Registry last updated
Apr 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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