A displacement measurement apparatus includes an ultrasound sensor transmitting ultrasounds to an object in accordance with a drive signal, and detecting ultrasound echo signals generated in the object to output echo signals; a driving and processing unit supplying the drive signal to the sensor, and processing the echo signals from the sensor to obtain ultrasound echo data; and a controller controlling the driving and processing unit to yield an ultrasound echo data frame at each of plural different temporal phases based on the ultrasound echo data obtained by scanning the object. The ultrasound echo data has one of local single octant spectra, local single quadrant spectra, and local single half-band-sided spectra in a frequency domain. The ultrasound echo data is obtained from plural same bandwidth spectra. A data processing unit calculates a displacement at each local position or distribution thereof in at least one of axial, lateral, and elevational directions by solving simultaneous equations derived at each local position via implementing a predetermined displacement measurement method on the ultrasound echo data yielded at the plural different temporal phases with respect to at least one of the axial, lateral, and elevational carrier frequencies and the phase, or the one of the local single octant spectra, the local single quadrant spectra, and the local single half-band-sided spectra.

An electrophysiology catheter is provided. In one embodiment, the catheter includes an elongate, deformable shaft having a proximal end and a distal end and a basket electrode assembly coupled to the distal end of the shaft. The basket electrode assembly has a proximal end and a distal end and is configured to assume a compressed state and an expanded state. The electrode assembly further includes one or more tubular splines having a plurality of electrodes disposed thereon and a plurality of conductors. Each of the plurality of conductors extends through the tubular spline from a corresponding one of the plurality of electrodes to the proximal end of the basket electrode assembly. The tubular splines are configured to assume a non-planar (e.g., a twisted or helical) shape in the expanded state.

A catheter has a distal assembly with at least one loop with ring electrodes. A single continuous puller wire for bidirectional deflection is pre-bent into two long portions and a U-shape bend therebetween. The U-shape bend is anchored at a distal end of a deflectable section which is reinforced by at least one washer having at least two holes, each hole axially aligned with a respective lumen in the deflectable section. Each hole is centered with a lumen so that each puller wire portion therethrough is straight and subjected to tensile force only. A proximal end of the support member is flattened and serrated to provide a better bonding to the distal end of the deflectable section.

A method of determining the perceptual load of a human brain. The perceptual load is induced by a predetermined task carried out by the human. The method includes the steps of: measuring with a functional near-infrared spectroscopy (fNIRS) sensor device a metabolic activity of the human brain while the task is carried out and determining the perceptual load as a function of a measured change in metabolic activity. The invention further relates to a method of determining the level of stimulus perception corresponding systems.

The invention features methods and devices for controlling bleeding from blood vessels that may be damaged as a result of trauma or impact with an object, such as a bullet or shrapnel. The device may be wearable by a user and include one or more components, such as wound sealant and multiple inflatable balloons/bladders. The device may be integrated into a garment, e.g., a vest, jacket, trousers, or full body suit. Once triggered (automatically or manually), the device may be used to deliver wound sealant to a wound site and/or pressure to the wound site by selective inflation of one or more balloons over exsanguinating blood vessels that may be damaged, thereby stopping or minimizing the bleeding. Alternatively, or in addition, the device may be used to stabilize a wounded wearer for, e.g., transportation purposes, or to provide buoyancy. Devices of the invention may also be used as a blood pressure monitor, as a massaging device, and as a breast pump. Devices and methods of the invention may also be used for repairing or stabilizing machines, such as vehicles (e.g., automobiles and boats).

There is provided herein a method for assessing a speech/lingual quality of a subject, the method comprising: providing a content-containing stimulus to a user; recording the user's vocal response to the stimulus and/or to instructions related thereto; processing the user's recorded vocal response to measure/extract/compute at least one linguistics (prosodic) parameter and at least one acoustic parameter; transforming the user's vocal response into a transformed text section, which is based on a processing unit's interpretation of the user's verbal response; comparing the transformed text section to a predetermined text section, which represents the user's expected; and computing an output signal indicative of at least one speech/lingual quality of the user, based at least on data resulted from the texts comparison, the at least one measured/extracted/computed linguistic parameter and the at least one acoustic parameter.

In certain embodiments, a headpiece 101 may contain the functional components described above integrated therein, and the headpiece may be releasably matable, The present invention relates to systems and methods for patient monitoring and intervention to prevent sudden unexpected death, as may occur in patients with epilepsy (SUDEP) or in infants as part of SUID, SIDS and/or suffocation. More specifically, the present invention provides a wearable device configured for monitoring a wearer and/or his environment, identifying and/or assessing death risk to the wearer, initiating communications to a caregiver that might provide an intervention or other treatment, and/or itself performing an action acting as an intervention to prevent death of the wearer. The wearable device includes particular sensors for gathering data from the wearer and/or the wearer's environment. Optionally, the wearable device may further include stimulators for delivering a death-preventing intervention stimulus to the wearer.

An electrophysiology catheter is provided. In one embodiment, the catheter includes an elongate, deformable shaft having a proximal end and a distal end and a basket electrode assembly coupled to the distal end of the shaft. The basket electrode assembly has a proximal end and a distal end and is configured to assume a compressed state and an expanded state. The electrode assembly further includes one or more tubular splines having a plurality of electrodes disposed thereon and a plurality of conductors. Each of the plurality of conductors extends through the tubular spline from a corresponding one of the plurality of electrodes to the proximal end of the basket electrode assembly. The tubular splines are configured to assume a non-planar (e.g., a twisted or helical) shape in the expanded state.

A loading device, a monitoring system, and a method thereof can measure stiffness of a structural member (SM) and monitor progress or property thereof over time. The loading device includes two types of displacement sensors, one type being an antenna. As the SM, which is in a magnetic or electromagnetic field and electromagnetically coupled to the antenna without contact, undergoes displacement under known loads, characteristics of the electromagnetic field coupling between the antenna and the SM change over time due to the displacement of the SM. The shift in the characteristics of the electromagnetic field coupling between the antenna and the SM can be used to determine the displacement of the SM. Based on the changes in the displacement over time, diagnosis of the SM being monitored over an evaluation period can be made. The loading device includes at least one movable frame to apply a preload to the SM.

A physiological signal monitoring device includes a base including a base body that has a bottom plate and an opening, a biosensor mounted to the base, and a transmitter removably mounted to the base body. The base further includes a first coupling structure disposed on a top surface of the bottom plate, and the transmitter includes a second coupling structure coupled to the first coupling structure when the transmitter is mounted to the base body. When the first and second coupling structures are coupled to each other, they are disposed to be distal from a periphery cooperatively defined by the base and the transmitter. They are uncoupled from each other when an external force is applied through the opening of the base body to separate the transmitter from the base.