Clinical Trial

A Clinical Study on the Effects of a Dietary Supplement on Stress, Anxiety, Mood and Sleep in a Pediatric Population

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Record status
This record was last updated July 22, 2025 (before its estimated August 15, 2025 completion). Its status may not reflect the trial's current state.
Summary
The study will be a randomized, placebo control clinical study to assess the the efficacy for improvement of mood/stress and anxiety compared to placebo through validated survey questionnaire. The target population of this study is 5 to 14 years old. Participants will be asked to take questionnaires to collect baseline at the beginning of the study. The questionnaires are: Perceived Stress Scale for children (PSS-ch), The Positive Affect and Negative Affect Schedule-Child Form-children (PANAS-children) and the Children's Sleep Habits Questionnaire (CSHQ). The interventional treatment will be for a total of 4 weeks (28 days). Participants will be asked to take the questionnaires at the end of the 28 days. The subjects will attend two appointments in the clinic throughout the duration of the study.
Trial Details
NCT Number NCT07076537
Lead Sponsor Olly, PBC
Conditions Healthy
Enrollment 80 participants
Start Date 2025-07-15
Primary Completion 2025-08-15 (estimated)
Study Completion 2025-09-02 (estimated)
Updated on ClinicalTrials.gov 2025-07-22