Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05177679 · ClinicalTrials.gov registry record · NA

Enhancing Children's Cognitive Function and Achievement Through Carotenoid Consumption

A NA study of Cognitive Change and Achievement, sponsored by University of Illinois at Urbana-Champaign.

Recruiting
Registry status
NA
Development phase
288
Enrollment target
1
Study location

NCT05177679 is a NA study of Cognitive Change and Achievement that is actively recruiting participants, run by University of Illinois at Urbana-Champaign. The registered enrollment target is 288 participants, above the 174-participant average among 44 other Cognitive Change trials with a reported enrollment target (66% higher). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05177679, a NA study of Cognitive Change and Achievement, is actively recruiting participants, sponsored by University of Illinois at Urbana-Champaign.

RECRUITING
Registry status
NA
Development phase
288 participants
Enrollment target
1
Study location

Study Summary

The aim of this study is to test the casual relationship between carotenoid supplementation, cognitive function, and achievement over a school-year. The central hypothesis is that, relative to the waitlist placebo group, children receiving the carotenoid supplement will exhibit greater gains in cognitive function and achievement.

Interventions

  • DIETARY_SUPPLEMENT Placebo control
  • DIETARY_SUPPLEMENT Active supplement

Study Locations (1)

Illinois

  • University of Illinois Urbana-Champaign - Urbana

Trial Details

FieldValue
Enrollment Target 288 participants
Start Date 2022-06-23
Est. Completion 2026-04-30
Phase NA

What the Registry Record Tells You About NCT05177679

The ClinicalTrials.gov registry entry for NCT05177679 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 288 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 174-participant average among 44 other Cognitive Change trials with a reported enrollment target (66% higher). The listed sponsor is University of Illinois at Urbana-Champaign, which has 129 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Cognitive Change appearing as the primary indexed condition, and to 2 interventions - of which Placebo control is the first listed.

NCT05177679 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT05177679 about?

NCT05177679 is a clinical study titled "Enhancing Children's Cognitive Function and Achievement Through Carotenoid Consumption". The aim of this study is to test the casual relationship between carotenoid supplementation, cognitive function, and achievement over a school-year. The central hypothesis is that, relative to the waitlist placebo group, children receiving the carotenoid supplement will exhibit greater gains in cogn...

What is the current status of trial NCT05177679?

This trial is currently recruiting. It is a NA study. The enrollment target is 288 participants. The study started on 2022-06-23. Estimated completion is 2026-04-30.

What conditions does trial NCT05177679 study?

This clinical trial studies the following conditions: Cognitive Change, Achievement, Macular Pigmentation.

What interventions are being tested in trial NCT05177679?

The interventions under investigation include: Placebo control (DIETARY_SUPPLEMENT), Active supplement (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT05177679?

This trial is sponsored by University of Illinois at Urbana-Champaign, which has 129 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05177679 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Cognitive Change

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.