A robust gray image encryption scheme using chaotic logistic map and artificial neural network (ANN) is introduced. In the proposed method, an external secret key is used to derive the initial conditions for the logistic chaotic maps which are employed to generate weights and biases matrices of the multilayer perceptron (MLP). During the learning process with the backpropagation algorithm, ANN determines the weight matrix of the connections. The plain image is divided into four subimages which are used for the first diffusion stage. The subimages obtained previously are divided into the square subimage blocks. In the next stage, different initial conditions are employed to generate a key stream which will be used for permutation and diffusion of the subimage blocks. Some security analyses such as entropy analysis, statistical analysis, and key sensitivity analysis are given to demonstrate the key space of the proposed algorithm which is large enough to make brute force attacks infeasible. Computing validation using experimental data with several gray images has been carried out with detailed numerical analysis, in order to validate the high security of the proposed encryption scheme.

We aimed to determine the neurophysiological pattern that is associated with the development of musculoskeletal pain that is induced by biomechanical constraints. Twelve (12) young healthy volunteers (two females) performed two experimental realistic manual tasks for 30 min. each: (1) with the high risk of musculoskeletal pain development and (2) with low risk for pain development. During the tasks, synchronized electroencephalographic (EEG) and electromyography (EMG) signals data were collected, as well as pain scores. Subsequently, two main variables were computed from neurophysiological signals: (1) cortical inhibition as Task-Related Power Increase (TRPI) in beta EEG frequency band (β.TRPI) and (2) muscle variability as Coefficient of Variation (CoV) from EMG signals. A strong effect size was observed for pain measurement under the high risk condition during the last 5 min. of the task execution; with muscle fatigue, because the CoV has decreased below 18%. An increase in cortical inhibition (β.TRPI >50%) was observed after the 5th min. of the task in both experimental conditions. These results suggest the following neurophysiological pattern—β.TRPI ≥ 50% and CoV ≤ 18%—as a possible indicator to monitor the development of musculoskeletal pain in the shoulder in the context of repeated and prolonged exposure to manual tasks.

This proof-of-concept study explores the potential of developing objective pain identification based on the analysis of electroencephalography (EEG) signals. Data were collected from participants living with chronic fibromyalgia pain (n = 4) and from healthy volunteers (n = 7) submitted to experimental pain by the application of capsaicin cream (1%) on the right upper trapezius. This data collection was conducted in two parts: (1) baseline measures including pain intensity and EEG signals, with the participant at rest; (2) active measures collected under the execution of a visuo-motor task, including EEG signals and the task performance index. The main measure for the objective identification of the presence of pain was the coefficient of variation of the upper envelope (CVUE) of the EEG signal from left fronto-central (FC5) and left temporal (T7) electrodes, in alpha (8–12 Hz), beta (12–30 Hz) and gamma (30–43 Hz) frequency bands. The task performance index was also calculated. CVUE (%) was compared between groups: those with chronic fibromyalgia pain, healthy volunteers with “No pain” and healthy volunteers with experimentally-induced pain. The identification of the presence of pain was determined by an increased CVUE in beta (CVUEβ) from the EEG signals captured at the left FC5 electrode. More specifically, CVUEβ increased up to 20% in the pain condition at rest. In addition, no correlation was found between CVUEβ and pain intensity or the task performance index. These results support the objective identification of the presence of pain based on the quantification of the coefficient of variation of the upper envelope of the EEG signal.