Clinical Trials Directory

Trials / Completed

CompletedNCT06654089

A Study Evaluating Quality of Life Parameters Following Use of Emergen-C

A Real-World Evidence Study Evaluating Quality of Life Parameters Following Use of Emergen-C

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
299 (actual)
Sponsor
HALEON · Industry
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine how Emergen-C use can improve quality of life (QoL) in a real-world setting to help consumers and healthcare professionals understand the benefits of taking Emergen-C on a routine or daily basis.

Detailed description

This will be a randomized, double-blinded, placebo-controlled clinical trial to evaluate the over-time effects of 12-weeks Emergen-C supplementation on QoL parameters in a real-world setting. This study will be entirely decentralized, and participants will not be required to physically attend any on-site visits. All study data will be collected remotely through a study platform using the participant's personal mobile device, tablet or computer. Sufficient participants will be screened to enroll approximately 300 eligible participants (approximately 150 participants per group) and approximately 240 participants are expected to complete the study (approximately 120 participants per group).

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTEmergen-C Core Super Orange PowderA dietary supplement powder containing vitamin C, zinc, vitamin B6, vitamin B12, folate, and manganese.
DIETARY_SUPPLEMENTPlaceboTo ensure proper blinding, the placebo was formulated to be indistinguishable from Emergen-C in taste, appearance, and other sensory characteristics. The placebo therefore contained fructose, and the electrolytes potassium, magnesium, calcium, and sodium.

Timeline

Start date
2024-10-30
Primary completion
2025-02-24
Completion
2025-02-24
First posted
2024-10-23
Last updated
2026-04-07
Results posted
2026-03-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06654089. Inclusion in this directory is not an endorsement.