NCT05564624 - Effect of Fasting-Mimicking Diet on Skin Health | Crick

Overview

This single-center, randomized, controlled clinical trial is being conducted to assess the efficacy on facial skin appearance of the Sponsor's 5-day meal kit when consumed monthly for 3 cycles over the course of 71 days by women with mild to moderate dry fine lines, lack of smoothness, uneven skin tone, and lack of radiance on the face.

Fasting-mimicking diet (FMD) was developed to mimic the metabolic effects of water-only fasting, while providing modest calories and essential nutrients. It consists of 100% natural ingredients, which are generally regarded as safe (GRAS). It is comprised of bars, soups, and beverages aiming to achieve consistent and effective short-term calorie restriction, while providing adequate micronutrients. The study will test the efficacy parameters, including clinical grading scores, Corneometer measurement, and Antera image analysis and subject self-assessment, of consuming the test products in place of other food over a 5 day period, for 3 cycles, over the course of 71 days when compared with baseline scores/values, and when compared to the untreated control.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

45

Conditions

Skin

Interventions

Fasting mimicking diet (FMD)OTHER

The ProLon(TM) Fasting Mimicking Diet regimen is a meal replacement plan that mimics water only fasting. It consists of 100% natural ingredients, which are generally regarded as safe (GRAS). It is comprised of bars, soups, and beverages aiming to achieve consistent and effective short-term calorie restriction, while providing adequate micronutrients. The very low protein and very low sugar content are essential characteristics of the diet. Complex carbohydrates and polyunsaturated fatty acids are its main components.

Eligibility

Sex: FEMALEMin age: 35 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Female, 35 to 60 years of age. 2. In good general health (physical, mental, and social well-being, not merely the absence of disease/infirmity), according to subject self-report. 3. Having mild to moderate (score of 3-6 according to a modified Griffiths scale,11 where 0=none and 9=severe) scores for the following parameters on the global face: Dry fine lines, Roughness/skin smoothness (visual), Uneven skin tone, Dullness/lack of radiance 4. Having a Body Mass Index in the range of 20-35 at the baseline visit. 5. Having not had any facial treatments in the past 6 months and are willing to withhold all facial treatments during the course of the study including facials, facial peels, photo facials, laser treatments, dermabrasion, botulinum toxin (Botox®), injectable filler treatments, intense pulsed light (IPL), acid treatments, tightening treatments, facial plastic surgery, or any other treatment administered by a physician or skin care professional designed to improve the appearance or firmness of facial skin. Waxing and threading are allowed but not facial laser hair removal. Exclusion Criteria: 1. Having known allergy or sensitivity to food or any component of the meal kit, including nuts, celeriac/celery, oats, and sesame. (Some of the products \[bars\] are processed in a facility where peanuts, eggs, soy, wheat, milk, and shellfish are also present.) 2. Breastfeeding, pregnant, or planning to become pregnant during the study according to subject self-report. 3. Having fasted (abstained from food) or having followed a very restricted food plan (eg, a cleanse or fast mimicking diet)for any period of more than 24 hours in the past 90 days. 4. Having a history of gastric bypass. 5. Having or having a history of a known, suspected, or diagnosed condition of disordered or restricted eating. 6. Currently experiencing menopause or having experienced menopause within the last 12 months. 9. Having a history of skin cancer within the past 5 years. 7. Having a health condition and/or pre-existing or dormant dermatologic disease on the test area/face that the Investigator or designee deems inappropriate for participation or could interfere with the outcome of the study. 8. Having observable sunburn, suntan, scars, nevi, excessive hair, tattoos, or other dermal conditions on the test areas that might influence the test results in the opinion of the Investigator or designee. 9. Having a history of immunosuppression/immune deficiency disorders, organ transplant, or currently using oral or systemic immunosuppressive medications and biologics and/or undergoing radiation or chemotherapy as determined by study documentation. 10. Currently using or having regularly used corticosteroids (systemic or topical, not nasal or ocular) within the past 4 weeks. 11. Having or having a history of diabetes, epilepsy, liver failure, advanced chronic kidney disease, heart failure, or syncope (fainting), or other metabolic disorder or serious health condition. 12. Having a risk for recurrent infections or currently experiencing a fever, cough, diarrhea, or active yeast infection. 13. Having a disease such as asthma, hypertension, hyperthyroidism, or hypothyroidism that is not controlled by diet or medication, or hypertension requiring treatment with more than one medication. Individuals having multiple or severe health conditions may be excluded from participation even if the conditions are controlled by diet, medication, etc. 14. Having started a long-term medication within the last 2 months. 15. Having any planned surgeries or invasive medical procedures during the study (including colonoscopy). Noninvasive medical procedures or surgeries will be reviewed for their impact on the study outcome and acceptability by the Investigator or designee. 16. Currently participating in any other clinical trial. 17. Having participated in any clinical trial involving the face within 2 weeks before study enrollment. 18. Having started hormone replacement therapies (HRT) or hormones for birth control or menopause less than 3 months before study enrollment or who plan on starting, stopping, or changing doses of HRT or hormones for birth control during the study. 19. Has any medical disease or condition that, in the opinion of the principal investigator (PI) or appropriate study personnel, precludes study participation.

Locations (1)

SGS Stephens, Inc

Richardson, Texas, United States

Outcomes

Primary Outcomes

Clinical grading of the facial skin

Clinical grading will be assessed on the indicated location on each subject's face using a modified Griffiths 10-point scale according to the following numerical definitions. Half-point scores may be used as necessary to more accurately describe the skin condition: 1. Skin smoothness (visual), cheeks; 2. Skin smoothness (tactile), cheeks; 3. Dry fine lines, global face; 4. Clarity, global face; 5. Redness, global face; 6. Evenness of skin tone, global face; 7. Radiance, global face; 8. Overall appearance of skin condition (health)

Time frame: Day 0 (baseline) and 71

Secondary Outcomes

Clinical grading of the facial skin

Clinical grading will be assessed on the indicated location on each subject's face using a modified Griffiths 10-point scale according to the following numerical definitions. Half-point scores may be used as necessary to more accurately describe the skin condition: 1. Skin smoothness (visual), cheeks; 2. Skin smoothness (tactile), cheeks; 3. Dry fine lines, global face; 4. Clarity, global face; 5. Redness, global face; 6. Evenness of skin tone, global face; 7. Radiance, global face; 8. Overall appearance of skin condition (health)

Time frame: Day 0 (baseline) and day 11

Facial skin hydration

Triplicate Corneometer (Corneometer CM 825, Courage + Khazaka electronic GmbH, Köln, Germany) measurements will be taken on the center of each subject's right cheek (at the intersection of lines extending up from the corner of the mouth and horizontally across the bottom of the nose). The Corneometer measures moisture content in the stratum corneum by an electrical capacitance method. The measurement has no units, but is proportional to the dielectric constant of the surface layers of the skin, and increases as the skin becomes more hydrated. The readings are directly related to the skin's electrical capacitance (picofarads).

Time frame: Day 0 (baseline) and day 11

Facial skin hydration

Triplicate Corneometer (Corneometer CM 825, Courage + Khazaka electronic GmbH, Köln, Germany) measurements will be taken on the center of each subject's right cheek (at the intersection of lines extending up from the corner of the mouth and horizontally across the bottom of the nose). The Corneometer measures moisture content in the stratum corneum by an electrical capacitance method. The measurement has no units, but is proportional to the dielectric constant of the surface layers of the skin, and increases as the skin becomes more hydrated. The readings are directly related to the skin's electrical capacitance (picofarads).