Study Summary
This trial will test if it's possible to study the effects of a supplement using at-home blood and urine samples, as well as online questionnaires.
Eligible Conditions
- Attention Deficit Hyperactivity Disorder (ADHD)
Treatment Effectiveness
Effectiveness Progress
Study Objectives
2 Primary · 7 Secondary · Reporting Duration: week 6
once, at baseline
Acceptability measured by a 'yes' response to their preference of using the Tasso device instead of a lab-based blood draw
Acceptability measured by a 'yes' response to their preference of using the at-home dried urine sample collection method instead of a lab-based urine sample collection method
Feasibility measured by count of participants who provide blood using the Tasso device
Feasibility measured by count of participants who provide the dried urine sample
week 6
Abbreviated Acceptability Rating Profile - 7 questions on a 6-point Likert scale
Acceptability measured by a 'yes' response to their preference of completing online remote study visits instead of in-person study visits
Feasibility measured by count of remaining Sticks
Feasibility of remote study visits measured by count of participants who complete all online remote study visits
Monitor participants for side effects by count of 'yes' if listed symptoms are new or have increased in severity, using the question format from the Pediatric Adverse Events Rating Scale
Trial Safety
Safety Progress
Trial Design
0 Treatment Group
20 Total Participants · 0 Treatment Group
Primary Treatment: Treatment · No Placebo Group · N/A
Trial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: week 6
Who is running the clinical trial?
Oregon Health and Science UniversityLead Sponsor
895 Previous Clinical Trials
6,831,285 Total Patients Enrolled
4 Trials studying Attention Deficit Hyperactivity Disorder (ADHD)
485 Patients Enrolled for Attention Deficit Hyperactivity Disorder (ADHD)
Jeanette Johnstone, PhDPrincipal InvestigatorOregon Health and Science University
Eligibility Criteria
Age 7 - 16 · All Participants · 6 Total Inclusion Criteria
Mark “Yes” if the following statements are true for you:You are medication and supplement free (if supplement ingredient is contained in the Lightning Stick) prior to study initiation.
You are willing to collect blood and urine samples once, at home.
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Conditions
Cancer Related
Treatments