Actively Recruiting
Testing a Digital Single-Session Intervention for Youths on the Waitlist for Psychotherapy
Led by Harvard University · Updated on 2025-08-15
226
Participants Needed
5
Research Sites
17 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
There is a significant unmet need for mental health care among youths in the United States, especially for conditions like depression and anxiety. The COVID-19 pandemic has increased this demand while reducing available clinicians and clinic resources, leading to long waitlists of up to 12 months for outpatient treatment. This trial evaluates a brief, digital single-session intervention teaching the principle of "Practicing the Opposite" (PTO) to help youths on psychotherapy waitlists, aiming to support them during these delays and reduce burden on mental health professionals. The intervention is a 30-45 minute online program using stories, interactive activities, and graphics to teach youths how practicing positive opposites of unhelpful behaviors can gradually improve their mood, thoughts, and actions. Participants are randomized to either the PTO intervention or usual waitlist procedures, which typically involve waiting and occasional check-ins. After removal from the waitlist, all participants receive standard clinic treatment. The PTO program includes four main parts: an introduction to the principle, testimonials, interactive practice activities, and planning for ongoing use. Participants aged 9 to 17 on outpatient waitlists will complete surveys and questionnaires at baseline, post-intervention, and during follow-ups up to one year or completion of clinic treatment. Outcomes include changes in anxiety and depression scales, behavior and feelings surveys, and ecological momentary assessments of mood and behavior changes. The study also monitors hope, perceived control, and clinical record data. This research aims to understand if the digital intervention helps youths while waiting and improves their mental health trajectory.
CONDITIONS
Brief Title
Digital Single Session Intervention for Youth Mental Health
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Youth or family has contacted a participating outpatient clinic to seek mental health care and is placed on the waitlist
- Youth is between 9 and 17 years old (inclusive) at enrollment
- Youth and at least one guardian consent to participation
- Youth reads English well enough to complete the digital program (takes classes in English)
- Youth has access to a digital device
You will not qualify if you...
- Youth is non-English speaking
- Youth does not have access to a digital device
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote) for eligibility assessment
Duration - One session lasting 30 to 45 minutes
Participants complete a single 30-45 minute digital session designed to help them practice positive behaviors to improve mood and engagement while on the waitlist for psychotherapy.
1 digital session (self-guided online)
Duration - Up to 1 year or until completion of clinic treatment
Participants are monitored through surveys and assessments over several months to evaluate changes in mental health symptoms and treatment engagement while awaiting or beginning routine clinical care.
Multiple follow-up assessments: post-intervention, 2-week, and monthly follow-ups
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
Research Team
K
Katherine Venturo-Conerly, A.M.
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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