Efficacy and Safety of Acute Topical and Aromatic Essential... | Clinical Trial | StuddyBuddy@endsection
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NCT07623811
Efficacy and Safety of Acute Topical and Aromatic Essential Oil-Based Products for Cognitive Support
Conditions: Healthy
Sex: All
Ages: 18 Years – 64 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 100
Sponsor: dōTERRA International
Summary
This study will evaluate whether the InTune product system may help support attention, memory, focus, and other thinking skills in healthy adults ages 18-64. Participants will be randomly assigned to receive either the InTune products or placebo products that look and feel the same but do not contain active ingredients. Participants will use the products throughout their participation in the study and complete a series of cognitive tests and questionnaires at the beginning and end of the study. Researchers will compare changes in memory performance, self-reported mental clarity and focus, product experiences, and any side effects between the two groups.
Eligibility Criteria
Inclusion Criteria:
* Able to read and understand English, willing to attend one study visit at the doTERRA campus in Pleasant Grove, UT
Exclusion Criteria:
* Regular use (topical, aromatic, or internal) of rosemary, copaiba, cedarwood, peppermint, wild orange, Spanish sage, lime peel, marjoram, litsea, agarwood, vetiver, hiba wood, elderberry extract, or vanilla essential oil in the past month
* Allergy or sensitivity to rosemary, copaiba, cedarwood, peppermint, wild orange, Spanish sage, lime peel, marjoram, litsea, agarwood, vetiver, hiba wood, elderberry extract, or vanilla essential oil
* Use of recreational drugs within the past month
* Color blindness
* Pregnancy, either currently or within the last 3 months
* Participation in a clinical trial within the past 30 days
* Medical conditions, medications, or allergies that could compromise safety or data integrity, as determined by the medical principal investigator
Source: ClinicalTrials.gov (NCT07623811). StuddyBuddy aggregates publicly available trial information.