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Pharmacogenomics of Stimulant Treatment Response

Attention-Deficit/ Hyperactivity Disorder (ADHD)

The "Pharmacogenomics of Stimulant Treatment Response" (PGx-STaR) study aims to identify genetic profiles related to methylphenidate treatment outcomes in children and adolescents aged 6-17 with Attention deficit/hyperactivity disorder (ADHD).

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    6 to 17

Participation Criteria

Inclusion Criteria:

Patients will be eligible for participation if all the following are true.

* Aged 6 - 17 years
* Located in Alberta, Canada.
* Primary diagnosis of ADHD (all types).
* Initiating methylphenidate (excluding immediate release (IR) forms) treatment for the first time.

Exclusion Criteria:

Patients will be excluded from participation if any of the following are true.

* Co-occurring psychotic, bipolar or eating disorders.
* Significant risk of suicide.
* An intellectual disability, or diagnosis of autism spectrum disorder (ASD) or tics/Tourette disorders.
* Past 12-month high-risk alcohol or substance use defined as monthly or more frequent use.
* Psychotherapy or brain stimulation-based therapy initiated within 8 weeks of referral or plans to initiate/change these types of therapies during the study
* History of liver or bone marrow (hematopoietic cell) transplant as these events can result in ambiguous genomic results.

Study Location

University of Calgary
University of Calgary
Calgary, Alberta
Canada

Contact Study Team

Backup Contact

Weng Sam Siu, MSPT

[email protected]
4038884774
Primary Contact

Madison Heintz, MSW

[email protected]
5875739747
Study Sponsored By
University of Calgary
Participants Required
More Information
Study ID: NCT06221358