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New treatment option for Cognitive Change
Official title Executive Function Training for Children and Adolescents
ClinicalTrials.gov ID: NCT07147894
What this study is testing
- What it's testing
- The goal of this clinical trial is to evaluate how different approaches to executive function (like adding game-like features, varying the number of tasks, and providing coaching) can enhance executive function outcomes in adolescents with and without ADHD. The main questions it aims to answer are: What components of executive function training contribute most to improving outcomes?
- Time commitment: about 4 weeks
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 12 to 17. Healthy volunteers may be eligible.
You may be able to join if
- 12-17 years old.
- Child must have a caregiver (parent/guardian) who is available to participate as a training aide.
- Child and parent/caregiver are able to understand/speak adequate English or Spanish to follow and participate in study procedures
- Both child and parent/guardian are willing to give informed consent/assent, be assigned by chance to either intervention condition, and be willing to...
- \~50% of the participants: Meet criteria for ADHD DSM-5 diagnosis.
You likely can't join if
- Child is taking ADHD medication/stimulants.
- Child has been formally identified as intellectually disabled.
- Abnormal visual acuity or hearing challenges that are prohibitive to participating in the intervention/assessment.
- History of organic mental disorders (conditions or disturbances that may be caused by injuries and/or neurodegenerative diseases affecting brain...
- Major sensory or motor impairment that would preclude valid cognitive testing.
- Participants with color blindness, if they are unable to discriminate the task relevant stimuli.
See the full eligibility criteria
- 12-17 years old.
- Child must have a caregiver (parent/guardian) who is available to participate as a training aide.
- Child and parent/caregiver are able to understand/speak adequate English or Spanish to follow and participate in study procedures
- Both child and parent/guardian are willing to give informed consent/assent, be assigned by chance to either intervention condition, and be willing to follow the assigned study protocol.
- \~50% of the participants: Meet criteria for ADHD DSM-5 diagnosis.
- Child is taking ADHD medication/stimulants.
- Child has been formally identified as intellectually disabled.
- Abnormal visual acuity or hearing challenges that are prohibitive to participating in the intervention/assessment.
- History of organic mental disorders (conditions or disturbances that may be caused by injuries and/or neurodegenerative diseases affecting brain tissues), psychosis, history of autism spectrum disorders, intellectual...
- Major sensory or motor impairment that would preclude valid cognitive testing.
- Participants with color blindness, if they are unable to discriminate the task relevant stimuli.
- Populations considered vulnerable such as wards and those with neurological or other health conditions that may prevent the ability to give informed consent.
The study team makes the final eligibility decision.
Where it's taking place
- Boston, Massachusetts, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 4 weeks per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling all sexes, 12 years to 17 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Boston, Massachusetts, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.