Important Information
Summary Information to Help you Decide Whether to Join this Study
| Field | Details |
|---|---|
| Study Title | See the impact Beem’s Blue Light Therapy has on your skin health! |
| Study Author | Ryan Junk, Jonathan DiBernard, Patrick Killen |
| Sponsor | This study is made possible by your payment to join. |
| Cost of Products, Services & Information to Participant | Prices for treatment vary from $139 to $709 depending on Beem membership status and package purchased. (There is no added cost to participate beyond the purchase of your beem package) |
| Included Products & Services | Access to Beem’s Blue Light Therapy device for the duration of the study, comprehensive tracking tools, personalized skin health reports, and ongoing support via help@efforia.com |
| Outcome Measures | Comprehensive Weekly Skin Health Self-Assessment, Dermatology Life Quality Index (DLQI), Your Goals & Objective Expectations in this Study. |
| Contact | help@efforia.com |
👍 The table above provides a summary. You may sign now and continue, or read more detail below.
Introduction & Summary
Welcome to this research study hosted on the Efforia platform. This study explores whether Beem’s Blue Light Therapy can improve your skin health, clarity, and overall appearance. Participation is voluntary, and you may withdraw at any time without penalty.
This study is observational, with participants acting as their own control. You will undergo twice-weekly, 20-minute light therapy sessions over 30 days. Your participation helps both your own understanding of how the therapy may work for you, and contributes to broader research knowledge.
Before deciding, please review the information carefully. If you have questions, contact help@efforia.com.
Purpose of the Study
The purpose of this study is to evaluate the effects of Blue Light Therapy, combined with Red and Infrared Light, on skin health.
- Blue Light (450nm) is believed to help reduce acne-causing bacteria and refresh skin appearance.
- Red Light (660nm) is associated with reducing inflammation and improving skin texture.
- Infrared Light (810nm) may stimulate deeper tissue and collagen production, supporting skin rejuvenation.
The study will assess outcomes using the Comprehensive Weekly Skin Health Self-Assessment, the Dermatology Life Quality Index (DLQI), and a Facial Skin Self-Assessment Survey.
What You Will Do as Part of this Study
While participating in this research study, you will need to:
- Be willing and able to follow the study directions and procedures
- Tell Efforia about any side effects or problems by communicating with help@efforia.com or online chat.
- Ask questions as you think of them, via help@efforia.com or online chat.
- Inform Efforia if you change your mind about staying in the study. You may leave the study at any time by communicating with help@efforia.com or chat.
Study activities:
- Duration: 30 days
- Sessions: 20 minutes, twice weekly
- First 5 minutes: Blue Light
- Next 5 minutes: Blue + Red + Infrared
- Final 10 minutes: Red + Infrared
- Assessments: Weekly skin health surveys, DLQI, Facial Self-Assessment
The Risks, Discomforts & Benefits of Being in this Study
This study involves minimal risk, but some participants may experience mild, temporary side effects.
Possible Serious Adverse Events & Side Effects
| Risk name | Risk likelihood | Summary |
|---|---|---|
| Skin irritation | Low | May cause temporary redness or irritation. |
| Eye strain | Low | Improper use without protective eyewear may cause discomfort. |
| Photosensitivity | Unknown | Individuals on light-sensitive medications may react negatively. |
Some People May be at Increased Risk
Some people may be at increased risk from this study and should consult with a healthcare provider before joining.
| Who | Why |
|---|---|
| Individuals with epilepsy | Light exposure may trigger seizures. |
| Individuals with photosensitivity | Light therapy could worsen reactions. |
| Individuals with eye conditions | Blue light may cause strain without adequate protection. |
| Pregnant, planning pregnancy, or breastfeeding | Safety data for this group is limited. |
Consider your Own Risk-Benefit Comfort Level
It is possible that not all risks and benefits are currently known. Participants have the responsibility to consult with their healthcare providers and conduct further research before enrolling in the study.
Privacy & Security Risks
We take strong measures to protect your data, but no system is completely risk-free. Please see Efforia’s privacy policy: https://efforia.com/privacy-policy.
Regulators (FDA or IRBs) may review your records. In rare cases, if we believe you are at risk of harm to yourself or others, we may reach out to local authorities.
The Possible Benefits of Participating
- You will receive personal results on your skin health.
- You will also receive aggregate study findings.
- There may be no measurable benefit other than learning whether or not the therapy impacts you.
What to do if you have a study related injury
If you experience an injury, seek local medical care immediately. After receiving care, contact help@efforia.com so that we can document and share information to improve safety.
Study related injury care and compensation
Efforia will not offer financial compensation nor absorb the costs of medical treatment should you be injured as a result of participating in this research. Efforia makes no commitment to provide free medical care or payment for any study-related injury as a result of participation in this study.
In the case of medical emergency
Call 911 immediately. Do not attempt to contact Efforia until after the emergency has passed. If you feel like you may be a danger to yourself or others, call 988 for the National Suicide Prevention hotline.
Alternatives to Participating in the Study
Since this is research only, your alternative is not to participate. You may also explore other Efforia protocols (including free options) by clicking the Efforia logo above.
Your Rights as a Participant
Your participation is voluntary. Refusing or withdrawing will not result in any penalty or loss of benefits.
- Privacy and Confidentiality: Your personal data is protected, though complete confidentiality cannot be guaranteed.
- Right to Your Own Results: You will receive full results after your involvement.
- Right to Leave: You may withdraw at any time via your profile. Refunds will be provided per Efforia’s return policy.
New Information and Study Results
If information generated from this study is published or presented, your identity will not be revealed. In the event new information becomes available that may affect the risk or benefit associated with this study or your willingness to participate in it, you will be notified so that you can decide whether or not to continue participating.
Conflict of Interest Statement
Efforia serves solely as the platform provider and does not sponsor or influence the study outcomes.
Efforia earns revenue by charging a transaction fee on the included services. Otherwise, we have no financial interest.
How we Reduce Conflicts of Interest
Participants must not have financial relationships (employee, investor, etc.) with the therapy providers.
Consequences of Conflict of Interest Non-Compliance
If a conflict is discovered, you may be suspended from the platform without refund.
By joining this trial, you affirm that you understand the above conflict of interest restrictions and agree to comply fully with them. Your participation is valued, and your adherence to these guidelines ensures the validity and reliability of our collective scientific efforts.
Data Protections
- Efforia will have access to your data, and may share with necessary partners (labs, devices).
- Your data will be used for personal reports and aggregate findings, never identified with your name without permission.
See privacy rights here: https://efforia.com/privacy-policy.
The researchers will only use and share information that is needed for the study.
The researchers will protect your information, as required by law.
Absolute confidentiality cannot be guaranteed because persons outside the study team may need to look at your study records.
The Efforia Institutional Review Board may review your study records, and other agencies, committees, and offices that review and monitor research studies. The purpose for using and sharing your information is to make sure the study is done properly.
By signing this consent form, you are giving permission for Efforia to use and share your health information. If you decide not to sign the form, you cannot be in the study.
California Experiential Research Subject’s Bill of Rights
You have additional rights as a California research subject. Please review our privacy policy.
Questions or Concerns
This study has been reviewed by the Efforia Institutional Review Board (IRB), a group of independent experts who help protect the rights, safety, and well-being of research participants.
If you have questions about your rights as a participant, or would like to speak with someone outside the research team, you can contact the IRB at ethics@efforia.com
Additional questions and closing
Efforia has approved the information in this consent form and have given approval to publish this study. This does not mean Efforia has approved or endorses you being in the study. You must consider the information in this consent form and do additional research based on your own situation for yourself and decide if you want to and are appropriate for this study.
If you have questions, please contact help@efforia.com. It is up to you to do additional research and talk to your physician before joining a study.