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NCT06834984 · ClinicalTrials.gov registry record · NA
Ritual Synbiotic+, a Dietary Supplement Designed to Impact Gastrointestinal Health, Mood, and Behavior in Women
A NA study of Gastrointestinal Disease Symptoms, sponsored by Colorado State University.
- Recruiting
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT06834984 is a NA study of Gastrointestinal Disease Symptoms that is actively recruiting participants, run by Colorado State University. The registered enrollment target is 60 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06834984, a NA study of Gastrointestinal Disease Symptoms, is actively recruiting participants, sponsored by Colorado State University.
- RECRUITING
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
The aim of this study is to determine how regular consumption of Synbiotic+, a dietary supplement that contains prebiotics, probiotics, and postbiotics, impacts functional gastrointestinal health, markers of intestinal inflammation and immune health, and influences mood and behavior. The primary outcome will be to assess gastrointestinal health using bowel movement tracking, self-report and objective assessments of gastrointestinal symptom severity, stool levels of short chain fatty acids, changes in the gut microbiota, including recovery of LGG and BB-12, and functional measures of the microbiome. Secondary outcomes will include stool and blood markers of gut barrier function and intestinal inflammation, immune health, and self-assessments of stress, anxiety, sleep, and quality of life.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Prebiotic, probiotic, postbiotic combination
Study Locations (1)
Colorado
- Colorado State University Food and Nutrition Clinical Research Laboratory - Fort Collins
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2025-05-01 |
| Est. Completion | 2025-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06834984
The ClinicalTrials.gov registry entry for NCT06834984 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Colorado State University, which has 94 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Gastrointestinal Disease Symptoms appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT06834984 reports 1 study location spanning 1 distinct geographic area - top geographies include Colorado.
Frequently Asked Questions
What is clinical trial NCT06834984 about?
NCT06834984 is a clinical study titled "Ritual Synbiotic+, a Dietary Supplement Designed to Impact Gastrointestinal Health, Mood, and Behavior in Women". The aim of this study is to determine how regular consumption of Synbiotic+, a dietary supplement that contains prebiotics, probiotics, and postbiotics, impacts functional gastrointestinal health, markers of intestinal inflammation and immune health, and influences mood and behavior. The primary out...
What is the current status of trial NCT06834984?
This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2025-05-01. Estimated completion is 2025-12-31.
What conditions does trial NCT06834984 study?
This clinical trial studies the following conditions: Gastrointestinal Disease Symptoms.
What interventions are being tested in trial NCT06834984?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Prebiotic, probiotic, postbiotic combination (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT06834984?
This trial is sponsored by Colorado State University, which has 94 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06834984 being conducted?
This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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