Innovative Alzheimer's Study: CareONE Concierge Seeks Participants
Exploring New Horizons in Alzheimer’s Care
CareONE Concierge is embarking on an important research study focused on the evaluation of an innovative wearable device designed to address cognitive difficulties tied to Alzheimer's disease. This device, known as the NeuroEM Therapeutics' TEMT-RF cap, is recognized as a Breakthrough Device by the FDA.
The Alzheimer's Challenge
Alzheimer’s disease represents an escalating challenge for families and healthcare providers alike, with current statistics estimating that nearly 7 million Americans are living with the condition. Projections suggest this number could rise to approximately 13 million by 2050. Traditional treatment options are often limited to addressing symptoms rather than the root causes of cognitive decline.
NeuroEM Therapeutics and TEMT-RF Cap
The TEMT-RF cap is a lightweight and non-invasive device that delivers electromagnetic waves similar to those emitted by cell phones. The purpose of this technology is to dismantle toxic clusters of proteins such as beta-amyloid and tau that are believed to contribute significantly to the progression of Alzheimer's disease. By targeting these harmful aggregations, there is potential to aid in restoring neuronal function and mitigating cognitive decline.
A Call to Participants
Peter Bechtel, the CEO of CareONE Concierge, expressed the impact Alzheimer's has on many families. "This study represents a significant milestone in combating Alzheimer's and dementia. Participants will not only have access to cutting-edge non-drug therapy but also help propel vital advancements in the treatment landscape for this condition."
This study aims to inclusively gather participants with mild to moderate Alzheimer's-related dementia. To participate, individuals will need to wear the TEMT-RF cap twice daily for an hour and adhere to a structured research protocol that includes cognitive assessments throughout the duration of the study.
Scientific Foundations of TEMT-RF
Dr. Edward Goodwin, the Chief Scientist at NeuroEM, has emphasized the foundational research supporting the TEMT-RF technology. “Our research indicates that this approach may influence key biological processes linked to Alzheimer’s disease. The data we gather from this study could significantly inform our understanding of how it affects cognitive health,” he remarked.
The Vision for Cognitive Health
Chuck Papageorgiou, CEO of NeuroEM Therapeutics, highlighted their collaboration with CareONE Concierge, stating, “We are dedicated to advancing safe and effective technologies for cognitive health. Studies like this are crucial for unlocking the full potential of TEMT-RF. As Alzheimer’s cases continue to rise, innovative research provides hope for patients and caregivers alike.”
How to Get Involved
CareONE Concierge is actively accepting participants for this groundbreaking study. For those interested in joining the study, please contact them directly for further details or application procedures.
About CareONE Concierge
CareONE Concierge is committed to providing innovative preventative healthcare solutions that cater to the needs of patients and the healthcare system. Their mission revolves around improving patient outcomes by collaborating with healthcare providers, emphasizing the importance of quality and revenue metrics.
About NeuroEM Therapeutics
NeuroEM Therapeutics is focused on reversing cognitive decline associated with Alzheimer’s through the development and clinical testing of bioengineered technologies. They are dedicated to groundbreaking research that is aimed at bringing transformative therapies to market, such as the TEMT-RF device for in-home use.
Frequently Asked Questions
What is the focus of the CareONE Concierge study?
The study evaluates the effects of a wearable device designed to alleviate cognitive symptoms associated with Alzheimer’s disease.
What is the TEMT-RF cap?
The TEMT-RF cap is a breakthrough non-invasive device that emits electromagnetic waves to disrupt harmful protein accumulations in the brain.
Who can participate in the study?
Individuals with mild to moderate Alzheimer’s-related dementia are eligible to participate in this research study.
How often will participants need to use the device?
Participants are required to wear the device twice daily for one hour as part of the study protocol.
What are the goals of the study?
The study aims to gather real-world data on the effectiveness of the TEMT-RF cap in improving cognitive function and overall brain health.
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