Recruiting PHASE4 ADHD

New treatment option for ADHD

Official title Stimulant vs. Non-stimulant Treatments and Reward Processing in Drug-naive Youth at SUD Risk

ClinicalTrials.gov ID: NCT03781765

What this study is testing

What is Methylphenidate?

Methylphenidate is an investigational medicine, given as a treatment applied to the skin, being studied as a potential treatment for adhd.

Also referred to as MPH.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
The study team will examine the effects of FDA approved stimulant and non-stimulant medications for ADHD, among youth with ADHD and with and without Oppositional Defiant Disorder (ODD) or Conduct Disorder (CD), on reward systems of the brain using fMRI.
  • Phase 4: studies an already-approved treatment

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 7 to 12

You may be able to join if

  • Pre-pubertal (e.g. Tanner stage 1 or 2)
  • Age 7-12 inclusive
  • Signed consent/assent
  • Parent communicates sufficiently in English to provide informed consent and complete assessment instruments;
  • ADHD as determined by computerized DISC (C-DISC) parent interview

You likely can't join if

  • Major neurological/medical illness
  • History of head injury
  • Fetal exposure to alcohol/drugs
  • Diagnosis of major psychiatric disorder (e.g., schizophrenia, bipolar disorder, major depression, generalized anxiety, social phobia, Tourette's...
  • Current suicidal ideation or past history of suicide attempt
  • Wechsler Abbreviated Scale of Intelligence (WASI)75 score \<75
See the full eligibility criteria
Who can join
  • Pre-pubertal (e.g. Tanner stage 1 or 2)
  • Age 7-12 inclusive
  • Signed consent/assent
  • Parent communicates sufficiently in English to provide informed consent and complete assessment instruments;
  • ADHD as determined by computerized DISC (C-DISC) parent interview
  • ADHD-Rating Scale-5 total score (interview with parent )
  • SNAP ADHD total score (teacher) of 1.5 SD \> age/sex norms
  • CD or severe ODD: CD or ODD + 2 symptoms of CD on C-DISC
  • SNAP ODD/CD subscale (parent and teacher) 1.5 SD \> age/sex norms
What rules you out
  • Major neurological/medical illness
  • History of head injury
  • Fetal exposure to alcohol/drugs
  • Diagnosis of major psychiatric disorder (e.g., schizophrenia, bipolar disorder, major depression, generalized anxiety, social phobia, Tourette's Disorder, PTSD, autism spectrum disorder)
  • Current suicidal ideation or past history of suicide attempt
  • Wechsler Abbreviated Scale of Intelligence (WASI)75 score \<75
  • Prior or current treatment with stimulants (prior or current treatment with non-stimulants is permitted, but participants must be off medication for 2 weeks at baseline)
  • Current or past alcohol/drug use (DISC interview; urine toxicology)
  • Psychological or medical condition which precludes being in the scanner (e.g., claustrophobia, morbid obesity)
  • Metal in the body that cannot be removed (e.g., braces, metal plate)
  • Visual disturbances that may impair task performance
  • Precocious puberty (e.g. Tanner stage \>2) or pregnancy Notes:
  • History of SUD in a 1st degree relative is permitted, and is expected in \~1/2 of the people
  • Ongoing psychosocial treatment is allowed but should not be initiated during the study

The study team makes the final eligibility decision.

Where it's taking place

  • New York, New York, 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 listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 7 years to 12 years. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include New York, New York, 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.