Actively Recruiting
A 6-Week Randomized, Double-Blind, Placebo-Controlled Virtual Study Evaluating an Olive Oil Extract on Knee Comfort and Function
Led by Applied Food Sciences Inc. · Updated on 2026-04-15
168
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
Sponsors
A
Applied Food Sciences Inc.
Lead Sponsor
A
Alethios, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating whether an olive oil extract can improve knee pain, discomfort, and function in adults aged 40 to 75 years who have experienced knee discomfort for at least three months. This study aims to understand if daily consumption of the olive oil extract affects participants' perceptions of knee pain and their ability to perform daily activities. The study uses validated questionnaires and functional movement tests to assess changes over time. Participants are randomly assigned to receive either an olive oil extract dietary supplement capsule or a matching placebo capsule once daily with food for six weeks. The olive oil extract capsules contain standardized olive-derived bioactive compounds, including oleocanthal and oleacein, while the placebo capsules are designed to look and taste similar but do not contain these active compounds. The study includes an initial acute assessment on day one and ongoing monitoring throughout the six-week supplementation period. During the study, participants complete digital questionnaires on knee pain, stiffness, and function at scheduled times and perform two simple functional movement tests at home. They are encouraged to wear a compatible activity-tracking device to collect daily physical activity and sleep data. Saliva samples are collected at home at specific timepoints to measure inflammatory markers. Participants also record any use of pain medications and report any side effects. The main outcome measured is the change in knee pain, with additional assessments of stiffness, physical function, joint status, activity levels, and inflammatory markers over the six-week period.
CONDITIONS
Brief Title
Examining Olive Oil Extract on Knee Comfort and Function
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 40 to 75 years
- Self-reported knee discomfort lasting at least 3 months
- Willing and able to take one study capsule daily for 6 weeks
- Willing and able to complete digital questionnaires and functional movement tasks
- Willing and able to wear a compatible activity-tracking device throughout the study
- Willing and able to collect saliva samples at home using provided kits
- Able to read and understand English
- Willing to provide informed consent electronically
You will not qualify if you...
- Diagnosis of inflammatory joint disease or other systemic inflammatory conditions affecting the knee
- Any current or prior diagnosis of knee disease by a licensed medical provider
- Knee surgery or significant knee injury within the past 6 months
- Planned knee surgery during the study period
- Known allergy or sensitivity to olive-derived products or any component of the study product
- Current use of investigational drugs or participation in another research study during the study period
- Any medical condition or circumstance that would make participation unsafe or interfere with study participation or data quality
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (virtual)
Duration - 6 weeks
Participants take one capsule of either olive oil extract or placebo daily with food for 6 weeks. They complete scheduled questionnaires and functional movement tasks, wear a compatible activity-tracking device, and record daily intake and rescue medication use.
Daily self-report and wearable device use, with assessments on Day 1 and Week 6
Trial Site Locations
Total: 1 location
1
Alethios, Inc.
San Francisco, California, United States, 94104
Actively Recruiting
Research Team
C
Christine Fields, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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