The Effect of Avocado vs. Usual Diet on Skin Aging
Completed · Not applicable
Conditions studied: Skin Inflammation
In brief
This clinical trial aims to assess the effect of providing one avocado per day on skin health in comparison with a control group maintaining their habitual diets. Participants will be randomly assigned to one of two equally sized groups. Both groups will be instructed to continue to follow their habitual diet but the intervention group will receive one avocado per day. Participants will be followed for outcomes for a four-month period.
Key facts
- Study ID
- NCT05102604
- Run by
- University of California, Los Angeles
- People needed
- 40
- Starts
- 2020-01-01
- Expected to finish
- 2020-12-30
- Last updated by the study team
- 2021-11-01
Who can join
Age: 25 and older, up to 90. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Female subjects
- Increased waist circumference defined as ≥35 inches for women (NCEP ATP III 2005)
- Women
- At least 25 years old at screening
- Not currently eating more than 2 avocados per month (habitual intake in U.S.)
- Non-smokers
- Fitzpatrick Skin type II-IV
- Willing to maintain their normal skin care pattern for the duration of the study (avoiding excessive sun, not beginning new skin treatments)
- Subjects must read and sign the Institutional Review Board-approved written informed consent prior to the initiation of any study specific procedures or enrollment
You may not qualify if…
- Does not eat avocados
- Sensitive / allergic to avocados
- Allergies to latex or oral allergy syndrome
- Not willing or unable to undergo MRI scans
- Unstable medical condition such as on dialysis for renal disease, cardiac, gastrointestinal, or hepatic disease, cancer (non-melanoma skin cancer >5 years ago acceptable, any cancer site >10yrs without recurrence).
- Pregnant, lactating, intention of pregnancy
- Lost or gained 10 lbs of body weight in last year
- Following restricted or weight loss dietary patterns
- Subjects who cannot avoid excessive exposure to either natural or artificial sunlight.
- Unstable anti-anxiety / anti-depressive / anti-psychotic medication use defined as dose change within last 6 months
- Currently taking any prescription medications that increase the risk of photosensitivity or history of taking such medications in the less than 3 months (e.g. alpha-hydroxy acids in cosmetics, antibiotics (ciprofloxacin, doxycycline, levofloxacin, ofloxacin, tetracycline, trimethoprim), antifungals (flucytosine, griseofulvin, voricanozole), antihistamines (cetirizine, diphenhydramine, loratadine, promethazine, cyproheptadine), Accutane
- Oral steroid use within the last 6 months longer than 7 days
- Elevated alcohol intake (7+ drinks/week females; 14+ drinks/week males)
- Participation in another clinical intervention trial within 30 days of baseline
Where it is running
- UCLA Center for Human Nutrition — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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