Actively Recruiting

Phase Not Applicable
Age: 9Years - 17Years
All Genders
Healthy Volunteers
NCT05449002

Digital Single Session Intervention for Youth Mental Health

Led by Harvard University · Updated on 2025-08-15

226

Participants Needed

5

Research Sites

264 weeks

Total Duration

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AI-Summary

What this Trial Is About

The aim of this study is to test the effectiveness of a single-session, digital intervention teaching the principle of practicing the opposite, when administered to youths on the waitlist for psychotherapy, with usual waitlist procedures as a control condition.

CONDITIONS

Official Title

Digital Single Session Intervention for Youth Mental Health

Who Can Participate

Age: 9Years - 17Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth/family has contacted a participating outpatient clinic to seek mental health care, and is placed on the waitlist.
  • Youth is between the ages of 9-17 years (inclusive) at the time of study enrollment.
  • Youth and at least one guardian consent to the youth's participation in study.
  • Youth reads English well enough to effectively complete the digital programs (defined as taking classes in English, as opposed to ESL classes).
  • Youth has access to a digital device.
Not Eligible

You will not qualify if you...

  • Youth is non-English speaking, as the program is only available in English.
  • Youth does not have access to a digital device.

AI-Screening

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Trial Site Locations

Total: 5 locations

1

Riley Child Psychiatry and Behavioral Sciences Clinic

Indianapolis, Indiana, United States, 46202

Actively Recruiting

2

Boston Child Study Center

Boston, Massachusetts, United States, 02116

Actively Recruiting

3

The Baker Center for Children and Families

Boston, Massachusetts, United States, 02120

Actively Recruiting

4

The Concord Center

Concord, Massachusetts, United States, 01742

Actively Recruiting

5

Riverside Community Care

Dedham, Massachusetts, United States, 02026

Active, Not Recruiting

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Research Team

K

Katherine Venturo-Conerly, A.M.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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