Joovvin' for Your Skin Health Study
Examining the Impact of Infrared Light Therapy Device on Cosmetic Skin Health
1 other identifier
interventional
63
1 country
1
Brief Summary
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)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2020
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 11, 2020
CompletedFirst Posted
Study publicly available on registry
July 15, 2020
CompletedStudy Start
First participant enrolled
August 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2021
CompletedFebruary 12, 2021
February 1, 2021
5 months
July 11, 2020
February 9, 2021
Conditions
Outcome Measures
Primary Outcomes (2)
Blinded Dermatology Assessment of Facial Skin Health
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
A custom self report survey on cosmetic skin health satisfaction
60 day
Study Arms (1)
Treatment Arm
EXPERIMENTALParticipants 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.
Interventions
Infrared light therapy uses certain wavelengths of light that are delivered to the face. This study will use the Joovv Mini.
Eligibility Criteria
You may qualify if:
- 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
- years old
- no serious medical conditions
- no medically treatable skin diseases
- willingness to take a selfie with mobile phone
You may not qualify if:
- Retinoid use
- prior use of light therapy within the past 6 months
- pregnant or nursing
- dietary supplements for skin, hair or nail health
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- ProofPilotlead
- Joovvcollaborator
Study Sites (1)
ProofPilot (Virtual Study: https://p.proofpilot.com)
New York, New York, 10003, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 11, 2020
First Posted
July 15, 2020
Study Start
August 1, 2020
Primary Completion
December 31, 2020
Study Completion
February 1, 2021
Last Updated
February 12, 2021
Record last verified: 2021-02