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ADHD clinical trials

View clinical trials related to ADHD.

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NCT ID: NCT06109051 Enrolling by invitation - ADHD Clinical Trials

EndeavorOTCâ„¢ Prospective Product Registry

Start date: October 3, 2023
Phase:
Study type: Observational [Patient Registry]

The EndeavorOTC product registry aims to collect real world data from EndeavorOTC users. The objectives of this registry are to describe clinical and demographic characteristics, treatment patterns, clinical and quality of life outcomes, and healthcare utilization in EndeavorOTC users in a real-world setting.

NCT ID: NCT05991167 Enrolling by invitation - ADHD Clinical Trials

EndeavorRx® Prospective Product Registry ("Expedition EndeavorRx")

Start date: June 1, 2022
Phase:
Study type: Observational [Patient Registry]

The EndeavorRx Prospective Product Registry aims to collect real world data from participants receiving the digital therapeutic, EndeavorRx, under conditions of routine clinical practice.

NCT ID: NCT05229627 Enrolling by invitation - ADHD Clinical Trials

Multimodal Magnetic Resonance Imaging Study on the Neural Mechanisms of Remission in Children With ADHD

Start date: January 2016
Phase:
Study type: Observational

Attention-deficit/hyperactivity disorder(ADHD) is highly prevalent among children and adolescents and often associated with poor long-term outcomes in adulthood. it is thus a serious public health problem. Methylphenidate(MPH) and Atomoxetine(ATX) are most frequently used for treating ADHD in many countries but the individual treatment response varies. Some patients present good response to either MPH or ATX with minimal or no symptoms left and optimal functioning(remission) after treatment, while others are poor responders to one of the two or even both. The underlying mechanism for the heterogenous responsiveness remains unknown. Thus we proposed to use multimodule magnetic resonance imaging(MRI) technology to explore the neural mechanisms of remission in children with ADHD treated with MPH or ATX.

NCT ID: NCT05137327 Enrolling by invitation - ADHD Clinical Trials

Classroom Behavior Support (CBS) Project

CBS
Start date: August 12, 2021
Phase: N/A
Study type: Interventional

The goal of the study is to conduct a randomized clinical trial to evaluate the impact of the Classroom Behavior Support Program (CBS; a multi-component, individually-tailored teacher consultation program) on teachers' classroom management practices (universal and targeted) and resulting student behavioral and educational outcomes relative to a best practices comparison consultation condition.

NCT ID: NCT04497363 Enrolling by invitation - ADHD Clinical Trials

Focused Ultrasound for the Treatment of ADHD Symptoms

Start date: July 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this open label study is to evaluate longer term tolerability and potential effectiveness of transcranial ultrasound in people with attention deficit hyperactive disorder (ADHD).

NCT ID: NCT04337905 Enrolling by invitation - ADHD Clinical Trials

Virtual Reality (VR) Diagnostic Tool for Attention Deficits/Hyperactivity Disorder (ADHD)

New
Start date: May 25, 2019
Phase: N/A
Study type: Interventional

Attention deficit/ hyperactivity disorder (ADHD) is a common neurodevelopmental disorder. The common diagnostic of ADHD is based on psychiatric examination and interview. So far, there is not any other diagnostic tool for ADHD nowadays. Therefore, virtual reality (VR) technology can be used as a stimulus, replacing real stimuli, recreating experiences, which are in the real world would be impossible. Consequently, ADHD-VR diagnostic tool development should be started to justify the ADHD diagnosis in psychiatric out-patient clinical services.

NCT ID: NCT03781752 Enrolling by invitation - Clinical trials for Attention Deficit Hyperactivity Disorder

Carboxylesterase 1 Genetic Variation and Methylphenidate in ADHD

Start date: March 4, 2018
Phase: Phase 4
Study type: Interventional

The study team will determine the association between d,l-methylphenidate (MPH) therapeutic outcomes in ADHD patients and genetic variants of CES1 and reveal key associations between CES1 genotypes and the PK and PD of MPH.

NCT ID: NCT03563573 Enrolling by invitation - ADHD Clinical Trials

Single-dose Potassium Supplementation in Patients With ADHD for Whom the Anesthetic Lidocaine is Ineffective

Start date: July 1, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

Randomized, controlled, double-blind trial of the effect of a single dose of potassium on ADHD symptoms as measured by changes in measures of symptoms of ADHD correlated with the results of their Lidocaine Effectiveness Test.