- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04471896
Joovvin' for Your Skin Health Study
February 9, 2021 updated by: ProofPilot
Examining the Impact of Infrared Light Therapy Device on Cosmetic Skin Health
Sixty day single arm trial examining self-report and remote dermatology assessment of cosmetic skin health after daily 10-20 minute sessions with an infrared light therapy device (the Joovv Mini)
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
63
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10003
- ProofPilot (Virtual Study: https://p.proofpilot.com)
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years to 78 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- willingness to use device for 60 days
- willingness to place security deposit on device of $149.99
- US resident with an address than can accept UPS deliveries
- 18 years old
- no serious medical conditions
- no medically treatable skin diseases
- willingness to take a selfie with mobile phone
Exclusion Criteria:
- Retinoid use
- prior use of light therapy within the past 6 months
- pregnant or nursing
- dietary supplements for skin, hair or nail health
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Treatment Arm
Participants will receive an infrared therapy device for use at home for 60 days.
Participants will use the device every day for 10-20 minutes during the intervention period.
|
Infrared light therapy uses certain wavelengths of light that are delivered to the face.
This study will use the Joovv Mini.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Blinded Dermatology Assessment of Facial Skin Health
Time Frame: 60 day
|
Comparison over timepoints of physician assessment of facial features at rest and smile to the Glogau & custom wrinkle selfie scale
|
60 day
|
Changes in Self-Report Skin, Hair & Nail Health and Satisfaction
Time Frame: 60 day
|
A custom self report survey on cosmetic skin health satisfaction
|
60 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2020
Primary Completion (Actual)
December 31, 2020
Study Completion (Actual)
February 1, 2021
Study Registration Dates
First Submitted
July 11, 2020
First Submitted That Met QC Criteria
July 14, 2020
First Posted (Actual)
July 15, 2020
Study Record Updates
Last Update Posted (Actual)
February 12, 2021
Last Update Submitted That Met QC Criteria
February 9, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2521
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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