MedTrace Logo

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

NCT06133231 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-01-16

No results posted yet for this study

Summary

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.

Conditions

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

Interventions

DIETARY_SUPPLEMENT

Multinutrients; a 36-ingredient blend of vitamins, minerals, amino acids, and antioxidants

Participants will take 2-4 capsules of EMP+ Advanced per day (max 8 capsules) for eight weeks.

Sponsors & Collaborators

  • Oregon Health and Science University

    lead OTHER

Principal Investigators

  • Jeanette Johnstone, PhD · Oregon Health and Science University

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
6 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-06
Primary Completion
2025-09-30
Completion
2026-01-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06133231 on ClinicalTrials.gov