Skin Inflammation
Conditions
Brief summary
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.
Detailed description
This study will be a randomized, parallel group comparison of daily avocado consumption vs. habitual diet. The study will be carried out in accordance with the guidelines of the Human Subjects Protection Committee of the University of California, Los Angeles. All subjects will give written informed consent before the study begins. At screening, informed consent and HIPAA authorization will be reviewed and signed. A medical history will be obtained. Enrollment will be reviewed by the study physician according to inclusion and exclusion criteria. Skin type and response to UVB will be assessed. At baseline, participants will undergo skin testing. Subjects will consume 1 avocado a day (Hass Avocado) or maintain habitual diet (up to 2 avocados/month) daily for 16 weeks. Skin will be assessed at weeks 0, 8 and 16. Each group will have 20 subjects as calculated by power analysis. Two additional subjects for each group will be recruited for possible dropouts and a total of 22 subjects will be recruited for each group.
Interventions
OTHERAvocado
Subjects will eat one avocado in addition to their usual diet
OTHERHabitual diet
Subjects will eat their usual diet
Sponsors
Hass Avocado Board
University of California, Los Angeles
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Masking description
Both groups will be instructed to continue to follow their habitual diet but the intervention group will receive one avocado per day
Intervention model description
Participants will be randomly assigned to one of two equally sized groups.
Eligibility
Sex/Gender
FEMALE
Age
25 Years to 90 Years
Healthy volunteers
Yes
Inclusion criteria
* 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
Exclusion criteria
* 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Minimal erythema | 16 weeks | Standardized inflammation will be induced by irradiating test areas on the inner arm of subjects with defined doses of narrow band ultraviolet B (NB-UVB) light delivered by the Dermalight 90 handheld device (National Biological). |
| Skin Elasticity | 16 weeks | The Cutometer measures the vertical deformation of the skin in millimeters when the skin is pulled by means of a controlled vacuum into the circular aperture, 6mm in diameter, of the probe. In its standard configuration, the Cutometer is equipped with a measuring probe with a 2mm aperture because the device is originally designed to measure only the elastic properties of the epidermis. Skin hydration will measured using the moisture/hydration probe that attaches to the Cutometer. We will measure six sites: forehead, under the eye, frontal cheek, crow's foot, lateral cheek, and inner forearm. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Skin Type Classification | 16 weeks | Developed in 1975, the system classifies skin type according to the amount of pigment the skin has and the skin's reaction to sun exposure. This information can help predict your overall risk of sun damage and skin cancer. |
Countries
United States
Outcome results
None listed