Actively Recruiting

Phase Not Applicable
Age: 13Years - 22Years
All Genders
NCT06004414

SilverCloud as a School-Based Intervention for Vulnerable Youth

Led by NYU Langone Health · Updated on 2026-03-30

120

Participants Needed

3

Research Sites

176 weeks

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this study is to test the efficacy and feasibility of a clinician-guided, app-based cognitive behavioral therapy (CBT) program, SilverCloud, as a school-based mental health intervention for vulnerable youth. An open trial of SilverCloud will be conducted to determine preliminary efficacy in this sample and inform program refinements by collecting outcome self-report assessments and conducting interviews on feasibility and acceptability. After the program and its implementation strategy are refined, we will conduct an randomized controlled trial. Adolescents who seek or are referred for mental health services through one of the study sites and screen positive for significant mental health symptoms will be randomized to receive SilverCloud or treatment as usual (TAU). Efficacy will be assessed through outcome self-reports. Feasibility and acceptability feedback will again be collected from participants, SBHC staff, and community members.

CONDITIONS

Official Title

SilverCloud as a School-Based Intervention for Vulnerable Youth

Who Can Participate

Age: 13Years - 22Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Enrolled in a high school
  • Score of 10 or higher on GAD-7 or PHQ-9
  • Speak and read English
  • For the randomized controlled trial: enrolled in 9th through 11th grades
  • For the randomized controlled trial: enrolled at one of the study sites
Not Eligible

You will not qualify if you...

  • Does not use a smartphone
  • Mental health concerns requiring intensive treatment, such as symptoms of mania or psychosis
  • Current suicidal thoughts with intent or plan
  • For the randomized controlled trial: current mental health treatment at one of the study sites within 1 month of enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Rutgers University

New Brunswick, New Jersey, United States, 08901

Not Yet Recruiting

2

NYU Langone Health

Brooklyn, New York, United States, 11220

Actively Recruiting

3

Northwell Health School Mental Health Partnership sites

Glen Oaks, New York, United States, 11004

Not Yet Recruiting

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Research Team

A

Anna Van Meter, PhD

CONTACT

E

Erum Nadeem, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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