Studies Enrolling Participants Ages 12-14
BRAIN-online Web-based Brain Assessment Study
Study description
The goal of this study is to use the information collected to develop more efficient ways of identifying cognitive and behavioral challenges in youth with prenatal alcohol exposure (PAE), and improve availability to high-quality diagnostic services for youth with PAE who may not otherwise have access.
Recruitment parameters
- Between the ages of 8-16
- FASD diagnosis or prenatal alcohol exposure
Study contact information
To learn more about the study, email our study coordinators, Mary Anthony, Kent Tuominen and Alex Doughty at [email protected].
Study keywords
FASD, FAS, pFAS, ARND, PAE, web-based
The BRAIN Study
Study description
This study obtains data from neuropsychological testing and brain imaging in boys at-risk for or with early-stage cerebral adrenoleukodystrophy (ALD) to uncover early, pre-clinical indicators of the disease. Data from these cohorts will be compared to data from typically developing boys to assess whether any neurocognitive changes precede or coincide with disease progression and development. Visits include the participant completing some activities on an iPad while caregivers fill out questionnaires assessing the behavior of their child and any caregiver stress/coping experiences.
Recruitment parameters
- Boys between the ages of 3-15
- EITHER have an ALD diagnosis OR are typically developing and healthy
Study contact information
To learn more about the study, email Rachel Floersch at [email protected].
Study keywords
ALD, typically developing, neuropsych testing, MRI, coping strategies
CBIT+TMS Study
Study description
The CBIT+TMS Study combines Comprehensive Behavioral Intervention for Tics (CBIT) and Transcranial Magnetic Stimulation (TMS). The goal of the study is to test if TMS can help make CBIT therapy even more effective. Research participation includes 5 assessment visits, 10 daily in-person CBIT+TMS sessions along with 3 MRI visits at the University of Minnesota.
Recruitment parameters
- Between the ages of 12-21
- Currently experiencing chronic motor and/or vocal tics
- Right-handed
- Must be able to undergo MRI
- Not currently receiving therapy focused on tics
- Not currently taking neuroleptic/antipsychotic medications
Study contact information
To learn more about the study, email [email protected] or call 612-626-5550.
Study keywords
Tics, tic disorders, Tourette syndrome, TMS, CBIT, comprehensive behavioral intervention for tics, Transcranial Magnetic Stimulation
FORWARD-MARCH (Fragile X Online Registry with Accessible Research Database-Multiple Assessments for Research Characterization)
Study description
The FORWARD-MARCH project will collect survey data from parents and caregivers and conduct several tests with participants to understand their cognition (thinking), language, behavior, and autism characteristics. About two years after your clinic visit for FORWARD-MARCH, we will ask you to repeat the same questionnaires and tests and make a clinic visit. This is because information is expected to change somewhat over time. This will help us learn how individuals with FXS change over time and as they age. You will receive a summary of your testing results from the assessments and can use these as needed to complement or inform school evaluations, or for other social or disability programming.
Recruitment parameters
Only individuals with FXS born between 2003-2020 are eligible to participate in FORWARD-MARCH. This includes participants who were previously enrolled in the FORWARD study and those new to FORWARD.
Study contact information
To learn more about the study, visit the webpage, email Desirae Rambeck at [email protected] or call 612-624-0183.
Study keywords
Fragile X Syndrome
Masonic Institute for the Developing Brain Positive Behavior Program
Study description
Researchers at the University of Minnesota Masonic Institute for the Developing Brain (MIDB) are looking for research participants for a study about interventions for physical aggression to others and/or self-injury in children with autism or another neurodevelopmental disability with co-occurring intellectual disability or global developmental delay. Parents will receive coaching and other supports to help reduce physical aggression to others and self-injury in their child.
Participants receive parent coaching for 30-60 minutes, 3x weekly for 16 weeks either in person at MIDB or through videoconferencing home visits. Participants then are followed for four visits across 6 months to see how they are doing. Questionnaires and interviews are given before, during, and after the intervention. Overall, parents commit to 16 months of participation in parent coaching and followup. Compensation is up to $450 per child/family.
Recruitment parameters
- Child is between 5-17 years old, has autism or another neurodevelopmental disability with co-occurring intellectual disability or global developmental delay, has delays in cognitive or communication skills
- Child experiences physical aggression to others and/or self-injury that occurs at least multiple times a week
Study contact information
To learn more about the study, email [email protected] or call Emily Hollerich at 612-365-0006.
Study keywords
Autism, intellectual disability, global developmental delay, self-injury, aggression, parent coaching
Neuromodulation and Exposure Therapy for Youth with OCD (NExT)
Study description
This study is designed to learn if transcranial magnetic stimulation (TMS), a type of non-invasive brain stimulation, can improve the outcomes of Exposure with Response Prevention (ERP), an existing therapy for OCD. All participants receive ERP. Treatment takes place daily (Monday-Friday) for about two weeks. Participants will also complete interviews, questionnaires, two brain scans (MRIs), and computer tasks. Participation in this study may last up to 12 weeks.
Recruitment parameters
- Between the ages of 12-21
- With OCD symptoms
- Right-handed
- Must be able to undergo MRI
Study contact information
To learn more about the study, email [email protected] or use our study interest form.
Study keywords
Obsessive-compulsive disorder, OCD, transcranial magnetic stimulation, TMS, pediatric clinical trial
Precision Longitudinal Brain-Behavior Mechanisms of Adolescent Executive Function: An Open Science MIDB Dataset (OpenEF)
Study description
The OpenEF Study explores how executive function (EF)—the ability to plan, focus, and regulate behavior—develops in adolescents and young adults. Participation includes weekly visits over 8 weeks with activities such as questionnaires, cognitive assessments, daily smartphone tasks, and optional MRI, blood, and smartwatch data collection.
Recruitment parameters
- Between the ages of 10-25
- Has not had any diagnosis, treatment, or current medication for psychiatric conditions within the past 12 months
Study contact information
To learn more about the study, email [email protected].
Study keywords
Executive Function, adolescents, MRI imaging, brain-behavior-biomarker study
Pharmacogenomics to Guide Antidepressant Selection in Adolescents
Study description
The purpose of this study is to investigate the influence of pharmacogenomic information on antidepressant selection and dosing for youth with depression. Pharmacogenomic test results will be evaluated and used to optimize antidepressant selection and dosing during this 12-week study. This will help clinicians better prescribe antidepressant medications for adolescents with depression.
Recruitment parameters
- Between 12-17 years of age
- Currently receiving treatment for depression at M Health Fairview Psychiatric Clinics
Study contact information
To learn more about the study, email [email protected] or call 612-625-4612.
Study keywords
Youth, depression, antidepressant, genetic testing
Trajectories of Change in Tourette Syndrome (QUEST)
Study description
QUEST is a Comprehensive Behavioral Intervention for Tics (CBIT) therapy trial for people aged 12-17 years who experience tics.
Recruitment parameters
- Between the ages of 12-17
- Presence of chronic motor and/or vocal tics, defined as tics for at least 1 year without a tic-free period of more than 3 consecutive months
- Tics must not be due to a medical condition or the direct physiological effects of a substance
- At least moderate tic severity, defined as a Yale Global Tic Severity Scale44 total score ≥14 (≥9 for those with motor or vocal tics only)
- Participants must be fluent in English to ensure comprehension of study measures and instructions.
- Without a previous diagnosis of psychosis or cognitive disability
- Without substance abuse or dependence within the past year
- Without current suicidal intent
- No changes in medication in the previous 6 weeks
Study contact information
To learn more about the study, email [email protected].
Study keywords
Tourette syndrome, tic disorders, tics, movement disorder, neurodevelopmental disorder
Transcranial Direct Current Stimulation (tDCS) & Cognitive Training Study
Study description
The goals of this clinical trial are to determine if children with FASD benefit from repeated sessions of computerized “games” designed to build attention, concentration, memory, and problem-solving and also to test whether mild electrical current on the scalp called transcranial direct current stimulation (tDCS) can improve learning during the computerized “brain training”.
Recruitment parameters
- Between the ages of 8-17
- With FASD diagnosis or prenatal alcohol exposure
Study contact information
To learn more about the study, email our study coordinators, Mary Anthony, Kent Tuominen and Alex Doughty at [email protected].
Study keywords
FASD, FAS, pFAS, ARND, PAE, tDCS, cognitive training
Multimodal Profiling of Response to Pediatric Comprehensive Behavioral Intervention for Tics (TReC Study)
Study description
The purpose of the TReC study is to identify who is most likely to benefit from CBIT, how CBIT changes the brain, and which parts of CBIT sessions are more helpful. This study will look at changes in tics over the course of treatment. By using neuroimaging methods such as EEG and fMRI, this study will add to the field's understanding of the neurological mechanisms that take place during CBIT and will assess which CBIT factors are most important for reducing tic symptoms.
Recruitment parameters
- Between the ages of 10-17
- With current chronic motor and/or vocal tics
- Must be able to undergo MRI and/or EEG
Study contact information
To reach our study team, call (612) 626-5544 or email [email protected]. Complete our contact form to connect with us!
Study keywords
CBIT, mental health, motor tic, tic, Tourette syndrome, vocal tic
Visual Biofeedback to Reduce Head motion During MRI Scans: Brainmapping Cohort
Study description
This study aims to help eliminate head motion in adolescents while they perform tasks in the MRI by providing participants with visual biofeedback on their performance.
Recruitment parameters
- Between the ages of 5-15
- With epilepsy and/or ADHD
- Must be able to undergo MRI
Study contact information
To learn more about the study, email Helayna at [email protected].
Study keywords
ADHD, adolescents, MRI task