Train Your Brain 2.0 - Improving Memory and Decision Making Among Youth
Train Your Brain 2.0: Improving Memory and Decision Making to Improve Outcomes Among Youth - A Randomized Controlled Trial
1 other identifier
interventional
72
1 country
2
Brief Summary
The goal of this clinical trial is to deliver a computer-based working memory training program to improve delay discounting (DD) and prevent substance misuse among at-risk adolescents in a traditionally underserved area. Results from the study will inform future substance use prevention efforts targeted at youth exposed to adverse childhood experiences. Findings will also refine future models of intervention delivery in traditionally underserved communities. The main aims of the project are are: 1\) To examine to examine changes in hypothesized mechanisms of substance use initiation and escalation, and 2) to assess whether changes in DD are a mechanism for reducing substance misuse during early adolescence. The investigators will evaluate whether changes in DD following active treatment predict substance use outcomes over the three-month follow-up period.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2024
Typical duration for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 16, 2024
CompletedFirst Posted
Study publicly available on registry
February 5, 2024
CompletedStudy Start
First participant enrolled
June 25, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
May 25, 2025
May 1, 2025
2.1 years
January 16, 2024
May 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Monetary Choice Questionnaire
The Monetary Choice Questionnaire (MCQ) is a measure of delay discounting (DD). Participants will be presented with two choices, one with a small, immediate monetary reward and the other with a larger, delayed monetary reward. They will be required to choose one of those rewards and their responses will be scored using reference discounting curves. A calculated score that places participants on steeper curves indicates higher levels of impulsivity and higher rates of DD. Scores are not bounded with a minimum and maximum value, but higher scores indicate worse outcomes and demonstrate the participant's preference to gain smaller rewards immediately over larger rewards with a time delay.
Baseline, 2 Weeks, 3 Months
Secondary Outcomes (8)
Change in Consideration of Future Consequences Scale
Baseline, 2 Weeks, 3 Months
Change in Digit Span
Baseline, 2 Weeks, 3 Months
Change in Stop Signal Task
Baseline, 2 Weeks, 3 Months
Changes in Letter Number Sequencing Test
Baseline, 2 Weeks, 3 Months
Change in Alcohol Effect Expectancies (Breif)
Baseline, 2 Weeks, 3 Months
- +3 more secondary outcomes
Study Arms (2)
Working Memory Training
EXPERIMENTALThe intervention is a computer-based training aimed at improving working memory in order to decrease delay discounting. Active training sessions include: Sequenced Recall of Digits - Auditory, Sequenced Reverse Recall of Digits - Auditory, Sequenced Recall of Digits - Visual, Sequenced Reverse Recall of Digits - Visual, Sequenced Recall of Words - Auditory, Sequenced Recall of Words - Visual, Sequenced Reverse Recall of Words - Auditory, Sequenced Reverse Recall of Words - Visual. Participants will complete at least 10 sessions with each session taking approximately 30 minutes to complete.
Working Memory
ACTIVE COMPARATORThe comparison control condition is a multi-session control computer training condition that is designed to not engage working memory during computer-based engagement sessions: Sequenced Recall of Digits - Auditory, Sequenced Reverse Recall of Digits - Auditory, Sequenced Recall of Digits - Visual, Sequenced Reverse Recall of Digits - Visual, Sequenced Recall of Words - Auditory, Sequenced Recall of Words - Visual, Sequenced Reverse Recall of Words - Auditory, Sequenced Reverse Recall of Words - Visual. Participants will complete at least 10 sessions with each session taking approximately 30 minutes to complete.
Interventions
A multi-session computer-based working memory training program to improve delay discounting and prevent substance use among at-risk adolescents in a traditionally underserved area.
A multi-session control computer training condition that is designed to not engage working memory among at-risk adolescents in a traditionally underserved area.
Eligibility Criteria
You may qualify if:
- Between the ages of 11 and 15 and have a parent/guardian willing to provide consent for their participation
- Proficient in English
- Willing to commit to participate in computer-based trainings over the course of 5-8 weeks (duration dependent on site)
- Access to internet services, cell phone, and/or email
- Willing to receive/send study-related text messages
You may not qualify if:
- Self-disclosure or identification with psychological disturbance, suicidality, or evidence of active suicide ideation
- Self-disclosure of current substance use disorder
- Provide consent for child's participation in study
- Proficient in English
- Access to internet services, cell phone, and/or email
- Willing to receive/send study-related text messages
- Self-disclosure or identification with psychosis, suicidality, or evidence of active suicide ideation
- Self-disclosure of current substance use disorder
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Freedom Schools Collaborative
Flint, Michigan, 48504, United States
Ernest T. Ford Recreation Center
Highland Park, Michigan, 48203, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 16, 2024
First Posted
February 5, 2024
Study Start
June 25, 2024
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
May 25, 2025
Record last verified: 2025-05