Testing Scalable, Single-Session Interventions for Adolescent Depression in the Context of COVID-19

Completed · Not applicable

Conditions studied: Depression

In brief

Most mental health problems emerge by age 14, often leading to chronic impairments and adverse impacts for individuals, families, and societies. Any action-focused path to reducing the need-to-access gap will require moving beyond the dominant settings, formats, and systems that have constrained intervention delivery to date. In a fully-online trial, youths ages 13-16 will be randomized to 1 of 3 self-administered single-session interventions (SSIs): a behavioral activation SSI, targeting behavioral MD symptoms; an SSI teaching growth mindset, targeting cognitive MD symptoms; or a control SSI. The investigators will test each SSI's relative benefits, versus the control, on depressive symptoms and proximal outcomes such as hopelessness. Results will reveal whether SSIs that were designed to address behavioral versus cognitive symptoms differentially benefit adolescents with elevated depressive symptoms.

Key facts

Study ID

NCT04634903

Run by

Stony Brook University

People needed

2452

Starts

2020-11-19

Expected to finish

2021-03-15

Last updated by the study team

2021-05-25

Who can join

Age: 13 and older, up to 16. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• are fluent in English
• have consistent internet and computer/laptop/smartphone access
• report elevated depressive symptoms (a score of >2 on the Patient Health Questionnaire-2 item version [PHQ-2])

You may not qualify if…

• fail to meet the above-listed inclusion criteria
• exit the study prior to condition randomization
• respond with either copy/pasted responses from text earlier in the intervention to any of free response questions
• obvious lack of English fluency in open response questions
• responding with random text in open response questions
• duplicate responses from the same individual in baseline or follow-up surveys
• We will also exclude for primary analyses (but may run sensitivity analyses including them) any participants who provide responses of fewer than 3 words to writing prompts that ask for at least 2 sentences or more.

Where it is running

• Stony Brook University — Stony Brook, New York, United States

Full record on ClinicalTrials.gov

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