Improving memory and decision-making in at-risk youth

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to deliver a computer-based working memory training program to enhance delay discounting and prevent substance misuse among adolescents aged 11 to 15 in underserved areas. The study will assess changes in delay discounting as a mechanism for reducing substance use during early adolescence, particularly among those exposed to adverse childhood experiences. Participants will engage in computer-based training over 5-8 weeks, with follow-up evaluations to determine the effectiveness of the intervention in improving cognitive skills and reducing substance use risk.

Why it matters

Who can join: the full rules

Adolescent Inclusion Criteria:

1. Between the ages of 11 and 15 and have a parent/guardian willing to provide consent for their participation
2. Proficient in English
3. Willing to commit to participate in computer-based trainings over the course of 5-8 weeks (duration dependent on site)
4. Access to internet services, cell phone, and/or email
5. Willing to receive/send study-related text messages

Adolescent Exclusion Criteria:

1. Self-disclosure or identification with psychological disturbance, suicidality, or evidence of active suicide ideation
2. Self-disclosure of current substance use disorder

Parent Inclusion Criteria:

1. Provide consent for child's participation in study
2. Proficient in English
3. Access to internet services, cell phone, and/or email
4. Willing to receive/send study-related text messages

Parent Exclusion Criteria:

1. Self-disclosure or identification with psychosis, suicidality, or evidence of active suicide ideation
2. Self-disclosure of current substance use disorder

Where it's running

• Freedom Schools Collaborative
  Flint, Michigan, United States Recruiting
• Ernest T. Ford Recreation Center
  Highland Park, Michigan, United States Recruiting

Study contacts

• Study coordinator: Julia Felton, PhD
• Email: Jfelton4@hfhs.org
• Phone: 7049957832

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.