Can a 15-Minute daily device zap and chill your way to better skin?
NCT ID NCT07510581
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing whether using a device that delivers microcurrent and cold therapy for 15 minutes each day can improve skin firmness, reduce wrinkles, and even out skin tone. About 100 adults aged 25 to 65 with mild to moderate skin concerns will use the device at home for 8 weeks. Researchers will measure changes through expert grading, special imaging, and participant feedback.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Apr 2026
An estimate. Start dates often move.
- Expected to finish
-
Jun 2026
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
25 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subject is female or male (approximately 85% female and 15% male) * Subject is between the ages of 25-65 (no more than 25% 55-65 per group) * Individuals with fine lines/wrinkles, lack of firmness, dullness, and uneven skin tone with a grade of at least 3 on a 10-point scale. * Individuals with sensitive skin. * Individuals who are able to cooperate with the Principal Investigator and study personnel throughout the duration of the study and are willing to comply with all study procedures, methods, evaluations, and study product use. * Individuals who are able to read and sign and informed consent. * Individuals who are able to receive emails on their cellular phones and are capable of completing electronic Informed Consents and/or Questionnaires on their device. * Individuals willing to be photographed and sign a model release. Exclusion Criteria: * Individuals who have had Botox in the last 3 months prior to Baseline. * Individuals who have had Filler (Including Lip Filler) in the last 6 months prior to Baseline. * Individuals with a history of atopic eczema, psoriasis, or onychomycosis. * Individuals who have used a topical or system medication within 14 days prior to Baseline. * Individuals who are on anti-acne drugs, topical and/or oral retinoids. * Individuals currently on GLP1 medications or other weight loss regimens. * Individuals who have used a beauty device of any kind in a clinical testing facility in the past 5 months prior to Baseline. * Individuals who have used self-tanners and/or tanning beds within 14 days prior to Baseline. * Individuals currently participating in other clinical studies that are testing a face product and/or device. * Individuals with uncontrolled medical condition(s), including dermatological problems, which could put them at risk in the opinion of the Principal Investigator or compromise the study outcome and/or chronic or serious diseases and conditions which would prevent participation in this clinical study such as cancer, AIDS, insulin-dependent diabetes, renal impairment, mental illness, and/or drug/alcohol addiction. * Individuals with a history of melanoma, or a treated skin cancer within the last 5 years. * Individuals who are pregnant, lactating, or planning to become pregnant. -Individuals who become pregnant during the study must inform the Principal Investigator immediately. * Individuals who are unreliable or unlikely to be available for the duration of the study. * Individuals with a history of allergic reactions, skin sensitization and/or known allergies to cosmetic and personal care products/ingredients. * Individuals who are immunocompromised. * Individuals who are employees of VCS, other testing firms/laboratories, consumer products, and/or raw goods manufacturers/suppliers. * Individuals who are unable to communicate or cooperate with the Principal Investigator/study personnel due to language problems, poor mental development, or impaired cerebral function. * Individuals who started hormones within the last three months preceding the commencement of the study. * Individuals who are using oral contraception for less than three months before study commencement or who have changed their contraceptive method within the three months before the Baseline visit or planning to modify their contraception treatment within the duration of the study. * Individuals who have regular salon and/or dermatological procedures that can interfere with study results (Microdermabrasion, Fillers, Facial Peels, etc.) and are not willing to stop throughout the study. * Individuals with facial tattoos and facial piercings (that can't be removed). * Individuals with tattooed/permanent make up (i.e., eyeliner, eyebrows, lip liner, etc.), eyebrow microblading, and/or eyelash extensions. * Individuals who plan to change their hairstyle throughout the course of the study or who wear hair coverings regularly (i.e., wigs, coloring, extensions, etc.).
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Skin health are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Validated Claim Support
Teaneck, New Jersey, 07666, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Apple peptides may speed skin healing after cosmetic procedures
- Could a gummy boost your gut, glow, and Get-Up-and-Go?
- A new serum aims to clear acne and boost skin confidence
- Could a daily powder boost skin elasticity and fight fatigue?
- Can a hyaluronic acid injection really boost skin health? new study aims to find out
- Ozone's hidden impact on skin revealed in new study