Attention Deficit Hyperactivity Disorder Clinical Trials
21 studies are recruiting for attention deficit hyperactivity disorder in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
Search these by distance from you
By city
Studies now recruiting
-
Developing Brain, Impulsivity and Compulsivity
Background: Impulsivity is acting 'without thinking.' Compulsivity is being overly inflexible. People vary in how impulsive or compulsive they are. Extreme versions of these behaviors play a role in mental disorders. Researchers want to study changes in the brain to learn more about these behaviors…
- Stage
- Not phased
- Ages
- 6 to 80
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Run by
- National Institute of Mental Health (NIMH)
-
A Study to Test the Effects of Centanafadine in Adults With Attention-deficit/Hyperactivity Disorder and Emotional Dysregulation
The primary purpose of this study is to evaluate the efficacy of centanafadine once daily (QD) extended-release (XR) capsules in adults with attention-deficit/hyperactivity disorder (ADHD) and emotional dysregulation (ED).
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Nola Research Works, New Orleans, Louisiana
- Locations
- 16 in total
- Run by
- Otsuka Pharmaceutical Development & Commercialization, Inc.
-
Evaluation of SPN-812 (Viloxazine Extended-release Capsule) in Preschool-age Children With ADHD
This study will evaluate the efficacy and safety of SPN-812 (viloxazine extended release) in children 4 to 5 years of age with ADHD.
- Stage
- Phase 4
- Ages
- 4 to 5
- Site
- The Center for Clinical Trials, Inc., Saraland, Alabama
- Locations
- 47 in total
- Run by
- Supernus Pharmaceuticals, Inc.
-
Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS)
The study investigators are interested in learning more about how drugs, that are given to children by their health care provider, act in the bodies of children and young adults in hopes to find the most safe and effective dose for children. The primary objective of this study is to evaluate the PK…
- Stage
- Not phased
- Ages
- 0 to 20
- Site
- Lucile Packard Children's Hospital, Palo Alto, California
- Locations
- 52 in total
- Run by
- Duke University
-
Trigeminal Nerve Stimulation for Children With Prenatal Alcohol Exposure
This is an open-label trial of trigeminal nerve stimulation (TNS) for children aged 8-12 years with attention deficit hyperactivity disorder (ADHD) putatively due to prenatal alcohol exposure (PAE). TNS has been successful in treating pediatric ADHD generally and it is US Food and Drug Administrati…
- Stage
- Not phased
- Ages
- 8 to 12
- Site
- University of California Los Angeles Semel Institute Division of Child & Adolescent Psychiatry, Los Angeles, California
- Run by
- University of California, Los Angeles
-
Development of Virtual Reality-based Interventions to Strengthen Cognitive Skillsets Related to Attention Deficit Hyperactivity Disorder (ADHD): A Pilot Phase I and Randomized Controlled Phase II Trial
Background: Children with attention deficit hyperactivity disorder (ADHD) often have cognitive problems. It may be hard for them to control their behaviors, concentrate for long periods, or make decisions. This can affect their education, friendships, and daily life. Virtual reality-based games may…
- Stage
- Phase 1
- Ages
- 8 to 16
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Run by
- National Institute of Mental Health (NIMH)
-
Enhancing Team Effectiveness for a Collaborative School-based Intervention for ADHD
The proposed project aims to integrate team-based implementation strategies with an established school-based intervention for children with ADHD, the Collaborative Life Skills Program (CLS), to enhance its implementation and optimize its effectiveness. The investigators will tailor three empiricall…
- Stage
- Not phased
- Ages
- 7 to 11
- Site
- IN STEP Children's Mental Health Center, San Diego, California
- Run by
- University of California, San Diego
-
Neurocognitive Effects of Non-Invasive Near-Infrared Light Stimulation
Inattentiveness and impulsivity in healthy adults and individuals with attention deficit hyperactivity disorder (ADHD) diminish these individuals' quality of life. Cortical hypometabolism has been hypothesized to contribute to inattentiveness in ADHD. Transcranial photobiomodulation (tPBM) is a saf…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The University of Texas at Austin, Austin, Texas
- Run by
- Francisco Gonzalez-Lima, PhD
-
Effects of Transcranial Photobiomodulation in ADHD
The investigators have previously shown that non-invasive methods of brain stimulation such as the administration of transcranial infrared light to the prefrontal cortex (PFC) can result in improvements to cognition and emotion as well as brain oxygenation. This method is called transcranial photob…
- Stage
- Not phased
- Ages
- 18 to 44
- Site
- The University of Texas at Austin, Austin, Texas
- Run by
- Francisco Gonzalez-Lima, PhD
-
Motor Attention Training for Attention Deficit Hyperactivity Disorder (ADHD)
The investigators will perform a feasibility/pilot trial of two non-pharmacological interventions for ADHD in college students.
- Stage
- Not phased
- Ages
- 18 to 23
- Site
- University of Wisconsin-Madison, Waisman Center, Madison, Wisconsin
- Run by
- University of Wisconsin, Madison
-
The Effects of Cannabigerol on Attention-Deficit/Hyperactivity Disorder
The goal of this clinical trial is to evaluate the effects of Cannabigerol (CBG) on indicators of Attention-Deficit/Hyperactivity Disorder (ADHD) in a sample of participants indicating/reporting symptoms associated with ADHD. The main question it aims to answer is: Does CBG reduce ADHD-related indi…
- Stage
- Phase 2
- Ages
- 18 to 55
- Site
- University of Arkansas, Fayetteville, Arkansas
- Run by
- University of Arkansas, Fayetteville
-
An Open-Label Treatment With Randomization Observation, Investigator-Initiated Study, on the Duration and Efficacy of Jornay PM (Methylphenidate Hydrochloride Extended-Release Capsules) on Adult ADHD Symptoms and Executive Function and Emotional Regulation Throughout the Day Into Early Evening
The goal of this study is to extend the efficacy evidence of sustained release methylphenidate compound (JornayPM) in adults with Attention-deficit/hyperactivity disorder (ADHD). JornayPM has recently been approved for treatment of patients 6 years and older with ADHD; the release mechanism is uniq…
- Stage
- Phase 4
- Ages
- 18 to 60
- Site
- NYU Langone Health, New York, New York
- Run by
- NYU Langone Health
-
A Pilot Study of a Remote ADHD Monitoring Program
RAMP is a pilot study examining the use of an Attention-Deficit/Hyperactivity Disorder (ADHD) Monitoring Program during the early stages of treating ADHD in children living in rural settings. This trial will enroll 36 caregiver/infant dyads across 2 sites and will evaluate feasibility endpoints rat…
- Stage
- Not phased
- Ages
- 5 to 11
- Site
- University of Mississippi Medical Center, Jackson, Mississippi
- Locations
- 2 in total
- Run by
- IDeA States Pediatric Clinical Trials Network
-
R61/33 - VR Study Phase 4
The goal of this larger parallel group randomized trial is to test the impact of a virtual reality program for improving the ability of emerging adults (age 18-25) with attention deficit hyperactivity disorder (ADHD) to stay focused while completing homework and studying. This study compares the im…
- Stage
- Phase 4
- Ages
- 18 to 25
- Site
- Louisiana State University, Baton Rouge, Louisiana
- Locations
- 2 in total
- Run by
- Rutgers, The State University of New Jersey
-
ADHD PreSMA Response Inhibition Therapy
ADHD children have abnormal inhibitory control, meaning they have trouble stopping themselves from doing something they should not do. This ability to control involves an area in the brain called the pre-supplementary motor area (pre-SMA). Scientists have previously shown that the pre-SMA is abnorm…
- Stage
- Not phased
- Ages
- 12 to 17
- Site
- Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
- Run by
- Children's Hospital Medical Center, Cincinnati
-
Transcranial Direct Current Stimulation (tDCS) Neuromodulation of Executive Function Across Neuropsychiatric Populations
In the current study, the investigators aim to understand the role of transcranial direct current stimulation (tDCS) in improving executive function across neuropsychiatric populations known to have deficits in this cognitive domain.
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Run by
- Massachusetts General Hospital
-
Project PEAK: Early Intervention for ADHD
Parent education is an effective and relatively cost efficient approach for reducing child behavior problems. Research, however, suggests that the effectiveness of parent education is mitigated by parent attendance and parent implementation of intervention strategies. That is, low attendance at par…
- Stage
- Not phased
- Ages
- 3 to 5
- Site
- Lehigh University, Bethlehem, Pennsylvania
- Run by
- Lehigh University
-
Focus Groups in Ethnically and Racially Diverse Families
Focus groups to identify treatment needs and barriers to participation in the planned multinutrient study among racially and ethnically diverse (Black and Hispanic) communities.
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- Oregon Health & Science University, Portland, Oregon
- Run by
- Oregon Health and Science University
-
Stimulant Effects on Disruptive Behavior
The goal of this study is to determine the effects of stimulant medication on disruptive behavior, function, preference and choice; however, it is primarily methodological and will add to current research by establishing an effective evaluation of the impact of stimulant medication on these behavio…
- Stage
- Phase 4
- Ages
- 4 to 12
- Site
- University of Iowa Hospitals and Clinics, Iowa City, Iowa
- Run by
- Matthew J O'Brien, PhD, BCBA-D
-
Optimizing Research With Diverse Families - Feasibility and Acceptability Study (FAST)
Evaluate feasibility and acceptability of recruiting Black and Hispanic families for an open label clinical trial of multinutrients while collecting real-time parent-reported child behavior data and collecting at-home biospecimens to explore their potential as biomarkers, in a study of pediatric AD…
- Stage
- Not phased
- Ages
- 6 to 17
- Site
- Oregon Health & Science University, Portland, Oregon
- Run by
- Oregon Health and Science University
-
A Trial of Dyanavel XR in Treating Co-occurring Fatigue Symptoms in Adults With Attention Deficit Hyperactivity Disorder (ADHD).
The goal of this clinical trial is to study the impact of Dyanavel on co-occuring fatigue in adults with Attention Deficit/Hyperactivity Disorder. The main question it aims to answer is whether Dyanavel XR leads to a statistically significant reduction in fatigue compared to placebo, as measured by…
- Stage
- Phase 4
- Ages
- 18 to 65
- Site
- Rochester Center for Behavioral Medicine, Rochester Hills, Michigan
- Run by
- Rochester Center for Behavioral Medicine
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.