Effects of dietary supplements and lifestyle changes on health markers in healthy adults
Wellness and Epigenetic Impact of a Natural Product Supplement System Combined With Lifestyle Modification
This study is testing if taking certain dietary supplements and making lifestyle changes can improve health markers in healthy adults aged 30 to 55.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 30 Years to 55 Years |
| Sex | All |
| Sponsor | dōTERRA International Industry-sponsored |
| Locations | 1 site (Pleasant Grove, Utah) |
| Trial ID | NCT06931977 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to investigate the impact of four dietary supplements and lifestyle modifications on gene expression and various health markers in healthy adults aged 30-55. Participants will consume the supplements daily for 12 weeks while also implementing changes to their diet, exercise, and sleep habits. The study will measure outcomes such as blood markers, anthropometric measurements, gut microbiome composition, and cognitive health. It will also assess the safety of the supplements and the efficacy of lifestyle modifications in enhancing health outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are healthy adults aged 30-55 who are willing to make lifestyle changes and participate in regular health assessments.
Not a fit: Patients with pre-existing health conditions or those currently taking essential oils, fish oil supplements, or probiotics may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into how dietary supplements and lifestyle changes can improve overall health and wellness in healthy individuals.
How similar studies have performed: While there have been studies on dietary supplements and lifestyle changes, this specific combination and approach is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults ages 30-55 years old * Willing to attend three study visits at Prime Meridian Health Clinic in Pleasant Grove, Utah * Willing and able to undergo three blood draws over 12 weeks * Willing to provide urine and stool samples three times over 12 weeks * Willing to wash out of all internally consumed essential oils or botanical products for at least 2 weeks prior to starting the study, and willing to maintain the washout for the duration of the study (14 weeks). * Willing to wash out of all fish oil supplements, probiotic supplements, and greens powder mix 2 weeks prior to starting the study, and willing to maintain the washout for the duration of the study (14 weeks). * Willing and able to consume study product as directed daily for about 12 weeks * Willing to track consumption of study product * Willing to implement changes to diet, exercise, and sleep habits for 12 weeks * Willing to avoid alcohol, recreational drugs, and smoking/vaping for the duration of the study (approximately 12 weeks) * Own a smartphone or tablet and willing to download the fitness tracker app * Willing to wear a fitness tracker for the duration of the study (approximately 12 weeks) * At least 110 pounds * No metabolic disease (BMI\>35, diagnosis and treatment of * hypertension, diabetes, or dyslipidemia) * No major diseases under treatment by doctor (Medical Reviewer's * discretion) * No pregnancy within the last 60 days or currently breastfeeding * (females) * No allergy to any of the ingredients in the study products * No regular internal consumption of the study products within the last 1 month (regularly is defined as dosing daily for more than 2 consecutive weeks, or dosing more than 2-3 times per week for 4 consecutive weeks) * No alcohol, recreational drug, or smoking/vaping use in the past 1 month * No evidence of medical condition, significant disease or disorder, medication, or surgery within the past 12 months that may, in the judgment of the medical provider, put the participant at risk or affect study results, procedures, or outcomes * Not currently or previously participating in any other clinical trial within the last 30 calendar days Exclusion Criteria: * Failure to meet all listed inclusion criteria
Where this trial is running
Pleasant Grove, Utah
- doTERRA International — Pleasant Grove, Utah, United States (Recruiting)
Study contacts
- Principal investigator: Nicole Stevens, PhD — doTERRA International LLC
- Study coordinator: Nicole Stevens, PhD
- Email: nstevens@doterra.com
- Phone: 8016157200
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.