A training method is provided to train changing muscle contribution in a human subject while the human subject is performing a complex movement. Feedback is provided in a simple understandable fashion by one or more data points calculated based on electromyography signals obtained over e.g. a stance phase of a walking cycle. The training method showed a significantly increased training effect in subjects performing these complex movements where these subjects were able to change the muscle activation given a specific goal. The training could be setup of a single muscle or multiple muscles. The data point feedback could be a measure for the single muscle or some relative measure for the multiple muscles. The training method results in improved coordination strategies and could be useful for retraining purposes as well as intervention methods for musculoskeletal pathologies or movement disorders.

Needle protector assemblies including needle assemblies and needle protectors for housing used blood collection needles are disclosed. The needle protectors are single-piece protectors that include an open distal end for receiving a needle hub (with a needle mounted thereon). A retaining member locks the needle hub when the needle hub is substantially retracted. A stop engages the needle hub in a fully retracted position such that a needle post is completely contained within an interior chamber of the needle protectors. A viewing slot in the needle protectors is provided.

Described here are meters and methods for sampling, transporting, and/or analyzing a fluid sample. The meters may include a meter housing and a cartridge. In some instances, the meter may include a tower which may engage one or more portions of a cartridge. The meter housing may include an imaging system, which may or may not be included in the tower. The cartridge may include one or more sampling arrangements, which may be configured to collect a fluid sample from a sampling site. A sampling arrangement may include a skin-penetration member, a hub, and a quantification member.

A lancet device includes a housing, a removable front cap mounted to the housing, a lancet holding member, a trigger and an arming system comprising a grippable cocking member structured and arranged to place the lancet device in a trigger-set or armed position. A depth adjustment system includes a member that is at least slidable and partially rotatably mounted and that has an axis of rotation arranged substantially parallel to a center axis of the lancet holding member. An ejection system includes an ejector having a portion extending outside a sidewall opening of the housing and being located closer to a front end of the housing than to a rear end of the housing. The sidewall opening of the housing is arranged on an area of the housing located between the trigger and a wall of the housing located opposite the trigger. The ejection system is structured and arranged to at least one of prevent axial movement of the lancet holding member or remove or eject a lancet from the lancet holding member.

A method is provided. The method includes identifying whether an amount of change in the pressure detected through an atmospheric pressure sensor is greater than or equal to a specified first threshold, in response to the amount of change in the pressure being greater than or equal to the first threshold, waking up a biometric sensor module including a plurality of electrodes in which some of the plurality of electrodes are disposed to come into contact with a body part of a user when the electronic device is worn, and others thereof are disposed to not come into contact with a body part of the user when the electronic device is worn, and identifying whether an interrupt signal, indicating that a state in which the plurality of electrodes are electrically connected is maintained for a specified first time or more, is received from the biometric sensor module.

This application relates to an automation compatible collection device for use in collecting samples, e.g., biological fluids and other samples. In some embodiments, the collection device can include a capillary for collecting samples from a biological location of a body and a cap configured to interface with an automation device.

An arrangement for producing a sample of body fluid from a wound opening created in a skin surface at a sampling site includes: a housing, the housing comprising a first opening; a skin interface member disposed in the first opening, the skin interface member comprising an inner member having a second opening, and an outer member at least partially surrounding the inner member and attached to the first opening; and at least one skin-penetration member configured and arranged to project within the second opening. Arrangements having alternatively constructed skin interface members are also described.

An integrated blood test unit including a blood collection recess, a test component, and a reservoir containing test fluid. The blood collection device moves to a delivery position under control of an actuator, which also releases test fluid from the reservoir onto the test component. Additional features are a window over the test outcome indicator, a blood delivery channel that only operates if the sample size is large enough, and a geometry for a lancet and actuator that is adapted for a self test situation.

Bodily fluid sample collection systems, devices, and method are provided. The device may comprise a first portion comprising at least a sample collection channel configured to draw the fluid sample into the sample collection channel via a first type of motive force. The sample collection device may include a second portion comprising a sample container for receiving the bodily fluid sample collected in the sample collection channel, the sample container operably engagable to be in fluid communication with the collection channel, whereupon when fluid communication is established, the container provides a second motive force different from the first motive force to move a majority of the bodily fluid sample from the channel into the container.

A needle assembly. The needle assembly enabling the analysis of fluid trapped in a flashback chamber after an insertion needle has been inserted into a patient's vein.