GrayMatters Health

About GrayMatters Health

GrayMatters Health develops Prism for PTSD™, the first FDA-cleared self-neuromodulation device that utilizes an amygdala-based digital biomarker to help patients regulate brain activity associated with post-traumatic stress disorder symptoms. This technology enhances standard mental health therapies, resulting in clinically significant symptom improvement for 67% of patients within three months of treatment.

```xml <problem> Many individuals suffering from Post-Traumatic Stress Disorder (PTSD) struggle to regulate the brain activity associated with their symptoms, even with standard mental health therapies. Current treatment options may not provide sufficient or targeted relief for all patients. </problem> <solution> GrayMatters Health offers Prism for PTSD™, an FDA-cleared, self-neuromodulation device designed to help patients learn to regulate brain activity linked to PTSD symptoms. The technology utilizes a digital biomarker based on amygdala activity to provide targeted feedback during therapy sessions. By augmenting standard mental healthcare, Prism aims to improve patient outcomes by enabling individuals to gain greater control over their neurological responses to traumatic memories and triggers. The device is intended for use under the guidance of a healthcare professional as an adjunct treatment. </solution> <features> - Self-neuromodulation device utilizing a digital biomarker of amygdala activity - Real-time feedback to help patients regulate brain activity associated with PTSD symptoms - Non-invasive and does not re-expose patients to trauma - Designed to augment standard mental health therapies - Clinically significant symptom improvement observed in 67% of patients within three months in clinical trials - Can be operated by a non-MD - Mild and self-resolved side effects </features> <target_audience> The primary users are mental healthcare professionals, such as psychiatrists and therapists, who treat patients with PTSD, as well as the patients themselves who are seeking adjunctive treatment options. </target_audience> ```

What does GrayMatters Health do?

GrayMatters Health develops Prism for PTSD™, the first FDA-cleared self-neuromodulation device that utilizes an amygdala-based digital biomarker to help patients regulate brain activity associated with post-traumatic stress disorder symptoms. This technology enhances standard mental health therapies, resulting in clinically significant symptom improvement for 67% of patients within three months of treatment.

How much funding has GrayMatters Health raised?

GrayMatters Health has raised 2700000.

Funding
2700000
Employees
35 employees
Major Investors
European Innovation Council

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GrayMatters Health

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Executive Summary

GrayMatters Health develops Prism for PTSD™, the first FDA-cleared self-neuromodulation device that utilizes an amygdala-based digital biomarker to help patients regulate brain activity associated with post-traumatic stress disorder symptoms. This technology enhances standard mental health therapies, resulting in clinically significant symptom improvement for 67% of patients within three months of treatment.

Funding

$

Estimated Funding

$2M+

Major Investors

European Innovation Council

Team (30+)

No team information available.

Company Description

Problem

Many individuals suffering from Post-Traumatic Stress Disorder (PTSD) struggle to regulate the brain activity associated with their symptoms, even with standard mental health therapies. Current treatment options may not provide sufficient or targeted relief for all patients.

Solution

GrayMatters Health offers Prism for PTSD™, an FDA-cleared, self-neuromodulation device designed to help patients learn to regulate brain activity linked to PTSD symptoms. The technology utilizes a digital biomarker based on amygdala activity to provide targeted feedback during therapy sessions. By augmenting standard mental healthcare, Prism aims to improve patient outcomes by enabling individuals to gain greater control over their neurological responses to traumatic memories and triggers. The device is intended for use under the guidance of a healthcare professional as an adjunct treatment.

Features

Self-neuromodulation device utilizing a digital biomarker of amygdala activity

Real-time feedback to help patients regulate brain activity associated with PTSD symptoms

Non-invasive and does not re-expose patients to trauma

Designed to augment standard mental health therapies

Clinically significant symptom improvement observed in 67% of patients within three months in clinical trials

Can be operated by a non-MD

Mild and self-resolved side effects

Target Audience

The primary users are mental healthcare professionals, such as psychiatrists and therapists, who treat patients with PTSD, as well as the patients themselves who are seeking adjunctive treatment options.

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