Are you COVID-19 Positive?

Help us

Help many

We are running a completely
remote and virtual clinical trial to test our investigational 
light therapy device (photobiomodulation device) to see if we can help people recover faster from COVID-19. 

Try a study device that may accelerate your recovery from COVID-19

Complete a short daily questionnaire online

Be a part of a new potential solution for treating COVID-19

 

Eligibility

To participate remotely, you must be:

18-65 years old

COVID-19 Positive

Within 10 days of your symptom onset

 

Study Treatment

It's simple and non-invasive.

Place one light-emitting diode (LED) of the study device on your chest and clip another small LED to one nostril for 20 minutes a day. Here's what we believe it may do for you:

May Accelerate Nitric Oxide Release
May Stimulate the Thymus Gland
May Increase Cellular Energy

May Act as an Anti-Inflammatory Therapy

Hover over text to learn more

Compensation

Participants

Referrals

Eligible participants will receive up to $500 for participation in the trial. 

If you are looking for information for friends and family, you could be eligible to receive a referral fee of $50 for every participant you refer. This will be paid to you if your referral meets the study eligibility criteria and is enrolled in this trial. 

 

Step 1

Registration

Click "Get Started" to create an account in our trial database called REDCap Cloud. REDCap Cloud is an international platform that complies with patient data privacy standards.

It takes about 15 minutes and will gather basic background information about you to determine if you qualify for our trial.

Watch our step-by-step video to help you with the registration process.

Enrollment Process

Step 2

Am I eligible?

If eligible, you will be allocated to one of two groups: the study treatment group or the control group.

Study Treatment Group

Vielight Device

Pulse Oximeter

Daily Survey

Paid up to $500

Control Group

Pulse Oximeter

Daily Survey

Paid up to $500

If you are assigned to the study treatment group, you’ll receive a Vielight device delivered to you home for your daily use. In either group, you will also receive a pulse oximeter and you'll fill out a daily survey telling us how you feel. This information is used to determine when your symptoms are gone, so that we know how long it took for you to get better. 

Step 3

Virtual Telehealth Visit

Once you are assigned to your group, we will contact you to have a telehealth call with one of our physicians right from the comfort of your own home. All you need is an internet connection, speakers, and a microphone on your phone, laptop, or tablet. 

Interested and have questions?

Our knowledgeable team of researchers will be happy to answer your questions. Please fill out the form or call to contact us. We respond within 24 hours. 

Study team: +1 800-517-8010

Study educator: +1 800-313-0899

By contacting us, you are requesting additional information regarding the trial participation and give us consent to contact you to provide such information.

 

Need more information?

References & Science

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Photobiomodulation Therapy Combined With Static Magnetic Field in Patients With COVID-19

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This study is sponsored by 

About Vielight Inc. and Photobiomodulation (PBM)

Vielight Inc. is a global leader in photobiomodulation (light therapy) research, innovation and its practical applications. Our devices are used by the U.S. Veterans Affairs, major universities, research labs, and tens of thousands of customers all over the world.

For more information about Vielight research in photobiomodulation please click "Learn More" below

 

Disclaimers

Any collected information is in compliance with Health Canada and US Health Care Privacy standards. For more information please click the link below

This website is for recruitment purposes only. No representation is made regarding the respective company in regards to efficacy until the trial has concluded. 

REDCap Cloud is a clinical trial data collection platform that complies with US, Canadian, and European patient data privacy standards. 

Copyright 2020 Vielight Inc. 

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