Evaluatation of a Microcurrent + Cold Therapy Device

StatusCompleted
PhaseNot applicable
Started

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Record History

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  1. Minor Trial status changed: Enrolling by Invitation → Completed Show 5 more changesShow less
    • Final enrollment: 112 participants (planned 100)
    • Study completion date changed from estimate of Jun 30, 2026 to Sep 1, 2026
    • Primary completion date changed from estimate of May 31, 2026 to Jun 10, 2026
    • Start date changed from estimate of Apr 1, 2026 to Mar 30, 2026
    • Eligibility criteria expanded, about 31 words
  2. Study First Submitted
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The present study aims to assess use of a microcurrent and cryotherapy device on skin health over an 8-week period using an at-home device that provides 15-minutes of microcurrent + cold therapy once daily. An additional aim is to assess the acute (i.e., single) use of microcurrent or microcurrent + cold therapy on measures of skin health. The primary question it seeks to answer is whether daily use of the TheraFace Pro Gen 2 alters facial skin characteristics. Secondary aims include collecting clinical images, professional photographs, and consumer perceptions of the device. Participants between the ages of 25-65 with various skin types will be enrolled for participation. Participants will visit the clinic three times for collection of outcome metrics at baseline with microcurrent therapy, baseline 2 using microcurrent + cold therapy, and 8 weeks after baseline. Measurements include: expert clinical grading, digital imaging, subjective assessment of skin, and clinical grade-images.
Trial Details
NCT Number NCT07510581
Lead Sponsor Therabody, Inc.
Collaborators: Validate Claim Support
Conditions
(from sponsor)
Skin Health
Enrollment 112 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov