Optimizing Research With Diverse Families - Feasibility and Acceptability Study (FAST)

Part of paid clinical trials in Portland, Oregon.

Sponsor
Oregon Health and Science University
Study ID
NCT06133231
Status
Recruiting
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Conditions

  • Attention Deficit/Hyperactivity Disorder
  • Emotional Dysfunction
  • Irritable Mood

Eligibility Criteria

Sex
ALL
Age
6 Years - 17 Years
Healthy Volunteers
Not accepted

Interventions

  • Multinutrients; a 36-ingredient blend of vitamins, minerals, amino acids, and antioxidants — DIETARY_SUPPLEMENT
    Participants will take 2-4 capsules of EMP+ Advanced per day (max 8 capsules) for eight weeks.

Study Details

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 ADHD.

Key Dates

Start date
Jan 6, 2024
Status verified
Jan 2025
Primary completion
Sep 30, 2025
Completion
Jan 31, 2026

Study Design

Enrollment
30 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Arms

  • Experimental: Multinutrient
    All participants will take the active multinutrient treatment

Primary Outcome Measure

Feasibility measured by count of consumed multinutrients [ Time Frame: Week 4, Week 8 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Oregon Health & Science UniversityPortlandOregon97239
Jeanette Johnstone, PhD
[email protected]
503-893-5873
Hayleigh Ast, ND (SUB_INVESTIGATOR)
Taryn Machingo, ND, MSc (SUB_INVESTIGATOR)

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