A probe device provides an enhanced bioelectric and spring-loaded sensing tip with an integrated force sensor. The probe device measures the bioelectric conductance value from a patient for therapeutic and/or diagnostic purpose using the spring-loaded sensing tip. In addition, the probe device measures the force applied by the spring-loaded sensing tip against the patient using the integrated force sensor. Using feedback from the force sensor and the bioconductive data of the patient, the force applied at the spring-loaded sensing tip may be adjusted to obtain improved results.

Presented herein are systems, methods, and devices that provide for stimulation of nerves and/or targets such as mechanoreceptors, tissue regions, mechanoresponsive proteins, and vascular targets through generation and delivery of mechanical vibrational waves. In certain embodiments, the approaches described herein utilize a stimulation device (e.g., a wearable device) for generation and delivery of the mechanical vibrational waves. As described herein, the delivered vibrational waves can be tailored based on particular targets (e.g., nerves, mechanoreceptors, vascular targets, tissue regions) to stimulate and/or to elicited particular desired responses in a subject.

A patient treatment unit and method analyzes and treats pain in tissues by applying an electrical pulse train to the affected tissue. The impedance of the affected tissue is measured, and the measured impedance is correlated to a level of pain in the patient. The pulse train is further applied in response to the measured impedance to reduce the patient's pain. The patient treatment unit includes a probe stimulus generator that outputs the pulse train. The treatment unit also includes a pair of probes for contacting the patient's body and receiving the pulse train. The pulse has improved shaping based on isolation of high voltage from a low voltage control. The unit further includes a body impedance analysis circuit that senses voltage and current via the probes when the probes are contacting the patient and observe the impedance. A monitor is electrically coupled to the body impedance analysis circuit and provides an indication of the measured impedance indicative of the patient's level of pain in real-time.

Devices, systems and methods are provided for treating migraine headaches and other conditions by non-invasive electrical stimulation of nerves and other tissue. A hand-held device includes a housing with a controller having a signal generator, an electrode for delivering electrical signals, and a conductive surface configured as a return path for the electrical signals. In certain implementations, the electrode is repositionable with respect to the housing. The patient can self-apply the hand-held device by pressing it against areas in need of pain relief. The device may include a pressure-sensitive gating switch to control delivery of the stimulation therapy. In certain embodiments, the electrode is a rollerball electrode. The device may include a chamber for retaining and dispensing conductive gel to the therapy site. In certain approaches, the device includes an electrode support for coupling an electrical stimulation system to the head for hands-free electrical stimulation therapy.

A CPR feedback system for assessing CPR carried out by a person on a subject and providing CPR feedback to the person, including an ECG system, a biosignal system, a CPR assessment system, and a CPR feedback unit. The CPR assessment system is configured to perform the steps (i) establish a reference ECG signal metric and a target biosignal metric, (ii) produce a CPR feedback signal, (iii) receive ECG signals measured during a plurality of chest compressions and use the ECG signals to establish a current ECG signal metric, (iv) receive biosignals and use the biosignals to establish a current biosignal metric, (v) compare the current ECG signal metric with the reference ECG signal metric and compare the current biosignal metric with the target biosignal metric, (vi) when the current ECG signal metric is less than the reference ECG signal metric and the current biosignal metric is less than the target biosignal metric, produce a CPR feedback signal, (vii) when the current ECG signal metric is less than the reference ECG signal metric and the current biosignal metric is equal to or greater than the target biosignal metric, increase the target biosignal metric and produce a CPR feedback signal advising the person to improve CPR performance, (viii) when the current ECG signal metric is equal to or greater than the reference ECG signal metric, set the reference ECG signal metric equal to the current ECG signal metric and produce a CPR feedback signal advising the person to maintain current CPR performance.

A method for treating chest wall injuries, including rib fractures, flail chest injuries or surgical incisions. The method comprising creating a localized airtight compartment external to the chest wall and fully covering the area of injury, varying the pressure within the compartment, and providing dynamic real-time counter forces that act reciprocal to the intrathoracic pressure changes that occur during ventilation. In a preferred embodiment, the apparatus has the capability of sensing the patient's chest wall motion created by ventilation, a pressure control component capable of varying the pressure within the airtight compartment such that it opposes pressure changes within the chest. The apparatus would be particularly useful in preventing the paradoxical movement of flail chest injuries. The method would also lessen pain experienced by patients with thoracic injuries such as rib fractures and post operative suffering.

Embodiments related to a haptic actuator for transmitting heat and/or mechanical vibrations to an adjacent surface are disclosed. The haptic actuator may include a heating membrane, one or more supports, and a body. The one or more supports may extend between the body and the heating membrane to physically separate the heating membrane from the body.

Methods and devices that reduce stress, anxiety and/or depression in a human using mechanical affective touch therapy is provided. In on embodiment, the method comprises (1) generating mechanical vibrations using a sinusoidal waveform and a mechanical transducer of a transcutaneous mechanical stimulation device in response to an applied electronic drive signal, (2) controlling the mechanical vibrations of the electronic drive signal by a controller board so that the mechanical vibrations have a frequency of less than 20 Hz; and (3) delivering the mechanical vibrations to the body of the human via the mechanical stimulation device, thereby providing the human with transcutaneous mechanical stimulation that reduces the human's anxiety, stress and/or depression.

A wireless teeth whitening system includes a mouthpiece that is devoid of any electrical circuitry so that it may easily be cleaned and sterilized. A control module may be coupled to the mouthpiece. This module has an electrical circuit board with LEDs and heating elements mounted on it. When the control module is coupled to the mouthpiece, the system may be used to whiten teeth. The control module includes a battery that may be inductively charged, and may be wirelessly controlled via Bluetooth from a mobile application.

Disclosed are materials, articles, devices, and methods for manufacture thereof that pertain to a tracheostomy support system. The tracheostomy support system can eliminate torque on the tracheostomy tube and offload pressure caused by the tracheostomy tube on the neck skin of a patient. Additionally, the tracheostomy support system can indicate when pressure or moisture on the skin is at an unsafe level that may predispose the patient to neck skin ulceration, breakdown, or infection. The tracheostomy support system can be automatically adjusted through a closed-loop feedback system or can be manually adjusted.