How to Read a Facial Device Study Without Being Fooled

Medically reviewed by

4 independent reviewers

Andrew Conrad Barile, Fisioterapeuta, Doctor en Terapia Física

Andrew Conrad Barile, Fisioterapeuta, Doctor en Terapia Física

Doctorado en Terapia Física (DPT), Fisioterapeuta Licenciado (PT)

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El Dr. Andrew Conrad Barile es Doctor en Terapia Física y CEO y Fundador de Xtreem Pulse LLC. Obtuvo su Doctorado en Terapia Física en Daemen College y aporta más de dos décadas de experiencia clínica y empresarial en terapia física pediátrica, terapia craneosacral e innovación en dispositivos médicos. Su profundo conocimiento de la anatomía humana, la fisiología muscular y la tecnología terapéutica ofrece un enfoque invaluable respaldado por la ciencia para la rejuvenecimiento facial y soluciones antienvejecimiento.

Bertica M. Rubio, M.D.

Bertica M. Rubio, M.D.

Director Médico, Clínica de Medicina Regenerativa y Antienvejecimiento | Médico Certificado por la Junta | Escuela de Medicina de Dartmouth

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La Dra. Bertica M. Rubio es una médica certificada y Directora Médica de la Clínica de Medicina Regenerativa y Antienvejecimiento en Redlands, California. Obtuvo su licenciatura en Ciencias en la Universidad Loyola Marymount y su título de Doctora en Medicina en la Escuela de Medicina de Dartmouth (Geisel School of Medicine). Completó su residencia en pediatría en el Centro Médico UC Irvine.

Con décadas de experiencia clínica, la Dra. Rubio se especializa en medicina para el manejo de la edad, medicina regenerativa, cicatrización de heridas y terapias con factores de crecimiento. Su práctica integra la ciencia médica basada en evidencia con tratamientos estéticos y regenerativos avanzados, ayudando a los pacientes a alcanzar una salud óptima y vitalidad juvenil.

La Dra. Rubio siente pasión por educar a los pacientes sobre la ciencia detrás del cuidado de la piel, el rejuvenecimiento facial y las tecnologías no invasivas como EMS (Estimulación Eléctrica Muscular) para el tonificado facial. Sus artículos para PureLift LAB combinan un conocimiento médico riguroso con orientación práctica para lograr resultados reales y duraderos.

Daniel Grinberg, MD, FACS

Daniel Grinberg, MD, FACS

Otorrinolaringólogo y cirujano de cabeza y cuello certificado | Miembro, Colegio Americano de Cirujanos | Profesor clínico asistente, Escuela de Medicina Mount Sinai

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Daniel Grinberg, MD, FACS, es un otorrinolaringólogo certificado por la junta y cirujano de cabeza y cuello en ENT and Allergy Associates en West Nyack, NY. Obtuvo su título de médico en la Facultad de Médicos y Cirujanos de la Universidad de Columbia, completó su residencia en Otorrinolaringología en el Centro Médico de la Universidad de Nueva York y es profesor clínico asistente en la Escuela de Medicina Mount Sinai. Es miembro de la American College of Surgeons y de la American Academy of Otolaryngology.

La perspectiva quirúrgica de cabeza y cuello del Dr. Grinberg ofrece a los lectores de PureLift LAB una visión clínica más amplia, conectando la práctica de EMS en casa con la anatomía médica subyacente con el mismo rigor científico que aplicamos a cada especificación del dispositivo.

Prof. Dr. med. Ivo Buschmann

Prof. Dr. med. Ivo Buschmann

Cátedra de Angiología, Hochschule Médica de Brandeburgo | Director de Clínica, Clínica Universitaria de Angiología, Hospital Universitario de Brandeburgo | Ex Consultor Senior, Charité Universitätsmedizin Berlín

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El Prof. Dr. med. Ivo Buschmann es Catedrático de Angiología en la Medizinische Hochschule Brandenburg Theodor Fontane (MHB) y Director Clínico de la Clínica Universitaria de Angiología en el Hospital Universitario de Brandeburgo. Completó su formación médica en la Universidad de Hamburgo, fue becario de la Sociedad Max-Planck en el Instituto Max-Planck de Investigación Cardiaca y Pulmonar, y ocupó cargos de consultor senior en la Charité Universitätsmedizin Berlin Campus Virchow antes de ser nombrado Catedrático en la MHB en 2016.

El Prof. Buschmann es una de las principales autoridades europeas en arteriogénesis — el crecimiento y remodelación de los vasos sanguíneos impulsados por el flujo — con más de 150 publicaciones revisadas por pares y varias patentes en EE. UU. y la UE sobre dispositivos que estimulan el crecimiento de vasos colaterales mediante terapia controlada de tasa de cizalladura. Su investigación conecta la estimulación mecánica y eléctrica con la adaptación vascular, la microcirculación y la perfusión tisular.

Las contribuciones del Prof. Buschmann aportan a los lectores de PureLift LAB una perspectiva de biología vascular que complementa nuestra autoría clínica, de fisioterapia y de anatomía quirúrgica existente — explicando cómo la estimulación EMS activa no solo los músculos faciales sino también la microcirculación que los abastece, y por qué la administración inteligente es tan importante a nivel del flujo sanguíneo como en la contracción muscular.

What's This About:

Almost every facial device brand cites something that looks like science, and most of it is a consumer survey wearing a lab coat.

This article compares the two on what decides the result you actually see, such as:

- One, was anything measured

- Two, was there a control group

- Three, how many people and for how long

- Four, who paid for it

- Five, was this device tested, or the category

and many more!

Apply them to our claims as well as anyone else's; we have tried to write this so that you can.

Key Points:

"96 percent of users agreed" is a satisfaction survey, not a measurement of anything on a face.

No control group means no way to separate the device from time, expectation and better lighting.

Twenty participants is a pilot; a hundred over twelve weeks is a study.

A study of the category is not a study of the product, and brands blur the two constantly.

Look for who funded it, and treat an undisclosed funder as the answer to that question.

One, was anything measured

The most common claim in this category is a percentage of users who agreed with a statement. That records an opinion after a purchase, which is a survey of hope as much as of anything else.

A measurement is a number taken off a face with an instrument: muscle thickness on ultrasound, a contour distance, a wrinkle depth score read by someone who does not know which group the photograph came from.

If the claim contains the words agreed, felt, noticed or reported, you are reading a survey.

Two, was there a control group

Without a comparison, everything that happens over twelve weeks is credited to the device: the better skincare people adopt when they start a routine, the improved sleep, the flattering second photograph, and simple expectation.

A sham-controlled study gives one group an inactive device, which is the only way to separate the effect from the belief. Chang and colleagues did exactly that in a double-blind design (10.3390/ijerph17113783).

A split-face design is the other good answer, treating one side and using the other as the control, which removes the person as a variable entirely. Kwak and colleagues used one (10.52660/jksc.2023.29.6.1505).

Three, how many people and for how long

Twenty participants over four weeks is a pilot, and a pilot tells you a study is worth running rather than telling you a result.

Kavanagh and colleagues followed 108 women for 12 weeks (10.1111/jocd.12007). That is the shape to compare against: enough people that individual variation averages out, and long enough for a tissue change to occur.

Be suspicious of any facial claim measured at two weeks, because muscle and collagen do not move that fast whatever the intervention.

Four, who paid for it

Industry funding does not invalidate a study and it does change how carefully you read it. What matters is disclosure: a paper that names its funder and its authors' affiliations is behaving properly.

A brand citing a study it commissioned, never published, and will not show you is telling you something by the omission.

Check for corrections too. Papers occasionally publish disclosures after the fact, and a corrected paper is not a discredited one; an uncorrected undisclosed conflict is worse.

Five, was this device tested, or the category

This is the one that catches everyone, including brands acting in good faith.

The studies above tested facial electrical stimulation as a category, under defined protocols, with research equipment. None of them tested a consumer device you can buy, ours included.

So the honest phrasing is that the category has been shown to do something under study conditions. The dishonest phrasing puts a brand name in front of that sentence, and it is worth noticing which one you are reading.

Six, does the number mean what it sounds like

A percentage improvement needs a baseline. Improving a score from 2 to 3 on an eleven-point scale is a fifty percent improvement and is also almost nothing.

Statistical significance means the result is unlikely to be chance; it does not mean the result is large enough to see in a mirror. Those are separate questions and a headline usually answers only the first.

Watch for the switch from an average to a maximum, where a study's best responder becomes the number on the box.

Seven, was the intervention isolated

If a study tests a device that combines stimulation with light, iontophoresis and cooling all at once, the study cannot tell you which of the four produced the change.

That is not a flaw in the study, which may have been asking a different question; it becomes a problem only when a brand quotes the result as evidence for one of the four.

Eight, does anyone disagree

A field where every published paper agrees is usually a field with a small literature. Papaiordanidou and colleagues report a case where frequency modulation did not deliver the expected benefit (10.1371/journal.pone.0084740), and it sits alongside Downey and colleagues, who found that it did (PMID 21996798).

A brand that cites the supporting paper and never mentions the contrary one is curating rather than informing.

Applying it here

Everything we cite is category evidence rather than a PureLift trial, and we say so on every page that cites it.

The specifications are the part that is specific to our devices, and those are checkable: 7 mA at 500 ohms for Face and Pro with a 4 microsecond pulse, 7.7 mA for Pro Edition, 9 mA for Pro Plus and GLOW, cleared under K190269, K230506, K221443 and K243587 respectively.

Ask any brand for those four things. The answer, or the absence of one, tells you a good deal before you read a single study.

For the full breakdown, see how the nine PureLift technologies work.

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