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NCT06889584 · ClinicalTrials.gov registry record · NA

Supplement Combination on Stress and Sleep

A NA study, sponsored by University of South Carolina.

Completed
Registry status
NA
Development phase
115
Enrollment target

NCT06889584: Completed NA study, sponsored by University of South Carolina.

NCT06889584 is a NA study that has completed, run by University of South Carolina. The registered enrollment target is 115 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06889584, a NA study, has completed, sponsored by University of South Carolina.

COMPLETED
Registry status
NA
Development phase
115 participants
Enrollment target

Study Summary

The purpose of this clinical trial is to assess the effects of a supplement combination on measures of sleep quality and stress in healthy adults.

Primary Outcome

To determine changes in perceived stress by way of the Cohen's Perceived Stress scale. The minimum is 0 and max is 40, with higher values meaning more stress.

Interventions

  • COMBINATION_PRODUCT All Active Supplement Combinations (Ashwagandha, Rhodiola rosea, magnesium threonate, L-theanine, and apigenin))
  • COMBINATION_PRODUCT AM Active Supplement Combination (Ashwagandha and Rhodiola rosea)
  • COMBINATION_PRODUCT PM Active Supplement Combination (Magnesium threonate, L-theanine, and apigenin)
  • OTHER AM and PM Placebo

Trial Details

FieldValue
Enrollment Target 115 participants
Start Date 2025-02-15
Est. Completion 2026-02-01
Phase NA
University of South Carolina

157 total trials

What the finished NCT06889584 record still lists

NCT06889584 is an interventional study that assigns participants to a tested intervention. The registered 115 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 4 interventions - of which All Active Supplement Combinations (Ashwagandha, Rhodiola rosea, magnesium threonate, L-theanine, and apigenin)) is the first listed.

NCT06889584 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06889584 about?

NCT06889584 is a clinical study titled "Supplement Combination on Stress and Sleep". The purpose of this clinical trial is to assess the effects of a supplement combination on measures of sleep quality and stress in healthy adults.

What is the current status of trial NCT06889584?

This trial is currently completed. It is a NA study. The enrollment target is 115 participants. The study started on 2025-02-15. Estimated completion is 2026-02-01.

What interventions are being tested in trial NCT06889584?

The interventions under investigation include: All Active Supplement Combinations (Ashwagandha, Rhodiola rosea, magnesium threonate, L-theanine, and apigenin)) (COMBINATION_PRODUCT), AM Active Supplement Combination (Ashwagandha and Rhodiola rosea) (COMBINATION_PRODUCT), PM Active Supplement Combination (Magnesium threonate, L-theanine, and apigenin) (COMBINATION_PRODUCT), AM and PM Placebo (OTHER).

Who is sponsoring clinical trial NCT06889584?

This trial is sponsored by University of South Carolina, which has 157 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06889584's enrollment target sits among peer trials

115 810th of 2000 higher than 1,190 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06889584, the US trial registry maintained by the National Library of Medicine. NCT06889584 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.