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NCT07196046 · ClinicalTrials.gov registry record · NA
Product Responsiveness to Enhanced Bioavailability Curcumin Dietary Supplements in Adults
A NA study of Quality of Life (QOL) and Joint Discomfort, sponsored by Ultra Botanica.
- Active
- Registry status
- NA
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT07196046 is a NA study of Quality of Life (QOL) and Joint Discomfort that is active but no longer recruiting, run by Ultra Botanica. The registered enrollment target is 30 participants, below the 143-participant average among 3 other Quality of Life (QOL) trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07196046, a NA study of Quality of Life (QOL) and Joint Discomfort, is active but no longer recruiting, sponsored by Ultra Botanica.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to evaluate whether distinct formulations of bioavailable curcumin supplements can improve joint comfort in adults who experience self-reported discomfort. Participants will also receive a placebo during the study, but they will not know when they receive it. The main questions it aims to answer are: * Do participants report improved joint comfort after taking each curcumin-based supplement? * Are there difference in quality-of-life scores or pain perceptions between the products? Researchers will compare the effects of the different formulations of bioavailable curcumin supplements to see if one provides greater improvements in joint comfort and related outcomes. Participants will: * Wear a fitness tracker starting at the time of electronic consent to provide continuous data on physical activity, heart rate, and sleep * Complete multiple blinded study periods involving different oral supplements, each separated by a washout period * Take one supplement twice daily during each intervention period, with intervention periods lasting between approximately two and four weeks * Complete washout periods of approximately one week between intervention periods * Complete the validated RAND-36 quality-of-life questionnaire and other study-specific questionnaires adapted from commonly used pain and global impression scales to assess joint comfort, pain perception, and overall health * Participate in a 30-day follow up period after the final supplement to complete final questionnaires and wearable data collection The study is conducted remotely using the Alethios decentralized research platform.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Supplement 2
- DIETARY_SUPPLEMENT Supplement 3
- DIETARY_SUPPLEMENT Supplement 1
Study Locations (1)
Oklahoma
- Ultra Botanica LLC - Oklahoma City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2025-12-10 |
| Est. Completion | 2026-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07196046
The ClinicalTrials.gov registry entry for NCT07196046 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 143-participant average among 3 other Quality of Life (QOL) trials with a reported enrollment target (79% lower). The listed sponsor is Ultra Botanica, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Quality of Life (QOL) appearing as the primary indexed condition, and to 3 interventions - of which Supplement 2 is the first listed.
NCT07196046 reports 1 study location spanning 1 distinct geographic area - top geographies include Oklahoma.
Frequently Asked Questions
What is clinical trial NCT07196046 about?
NCT07196046 is a clinical study titled "Product Responsiveness to Enhanced Bioavailability Curcumin Dietary Supplements in Adults". The goal of this clinical trial is to evaluate whether distinct formulations of bioavailable curcumin supplements can improve joint comfort in adults who experience self-reported discomfort. Participants will also receive a placebo during the study, but they will not know when they receive it. The ...
What is the current status of trial NCT07196046?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2025-12-10. Estimated completion is 2026-08.
What conditions does trial NCT07196046 study?
This clinical trial studies the following conditions: Quality of Life (QOL), Joint Discomfort.
What interventions are being tested in trial NCT07196046?
The interventions under investigation include: Supplement 2 (DIETARY_SUPPLEMENT), Supplement 3 (DIETARY_SUPPLEMENT), Supplement 1 (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT07196046?
This trial is sponsored by Ultra Botanica, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07196046 being conducted?
This trial has 1 study location across Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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