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Cognitive Training Video Game to Target Subclinical Depressive Symptoms in Youth

University of Michigan logo

University of Michigan

Status

Completed

Conditions

Depression
Subclinical Depressive Symptoms

Treatments

Device: Computerized cognitive training (CCT) using EndeavorRx

Study type

Interventional

Funder types

Other

Identifiers

NCT05697627
HUM00227345

Details and patient eligibility

About

The purpose of the study is to determine how cognitive control training (CCT) changes behavior in youth with subclinical depressive symptoms. This research will show what types of behavior changes are important for CCT to help reduce depressive symptoms. In the future, this information will be used to try to improve prevention of the development of depression, so that it can help more patients.

Full description

The primary study investigator acknowledges contributions from Kate Fitzgerald, Emily Bilek, Christopher Monk, and Adriene Beltz.

Enrollment

31 patients

Sex

All

Ages

9 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria:

  1. Parent or guardian willing to give informed consent, and children willing to give informed assent to participate in the study.
  2. Males and females (age 9 - 17.99)
  3. Participant is willing to engage in a technology-based intervention (technology will be provided to participants who live in the state of Michigan, if not already accessible to participant).
  4. Self-reported depressive symptoms (Children's Depression Inventory [CDI] score between 3-19 at Assessment 1)
  5. Participants will be required to maintain a stable dose of medications

EXCLUSION CRITERIA

  1. Color blindness
  2. Unable to play the video game for any reason
  3. Current Kiddie Schedule for Affective Disorders and Schizophrenia (K-SADS) diagnosis of clinical depression, psychosis, or Autism Spectrum Disorder
  4. Has enrolled in new psychotherapy (for the treatment of a mood or anxiety disorder) or had changes to their psychotherapy in the 4-weeks prior to study enrollment
  5. Endorses items #1, #2, #3, #4, #5, or #6 on the Columbia Suicide Severity Rating Scale (C-SSRS) Screener (Past-Month); i.e., has present suicidal intention/behavior.
  6. Has had any changes to their medication in the 4-weeks prior to study enrollment

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

31 participants in 1 patient group

Computerized cognitive training (CCT) using EndeavorRx
Experimental group
Description:
Exciting, youth-friendly computer game, EndeavorRx engages and trains cognitive control across component processes of attention, response inhibition, shifting and working memory.
Treatment:
Device: Computerized cognitive training (CCT) using EndeavorRx

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Hannah Becker, M.S.

Data sourced from clinicaltrials.gov

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