Objective. Brain–computer interface (BCI) systems can be employed to provide motor and communication assistance to patients suffering from neuromuscular diseases, such as amyotrophic lateral sclerosis (ALS). Movement related cortical potentials (MRCPs), which are naturally generated during movement execution, can be used to implement a BCI triggered by motor attempts. Such BCI could assist impaired motor functions of ALS patients during disease progression, and facilitate the training for the generation of reliable MRCPs. The training aspect is relevant to establish a communication channel in the late stage of the disease. Therefore, the aim of this study was to investigate the possibility of detecting MRCPs associated to movement intention in ALS patients with different levels of disease progression from slight to complete paralysis. Approach. Electroencephalography signals were recorded from nine channels in 30 ALS patients at various stages of the disease while they performed or attempted to perform hand movements timed to a visual cue. The movement detection was implemented using offline classification between movement and rest phase. Temporal and spectral features were extracted using 500 ms sliding windows with 50% overlap. The detection was tested for each individual channel and two surrogate channels by performing feature selection followed by classification using linear and non-linear support vector machine and linear discriminant analysis. Main results. The results demonstrated that the detection performance was high in all patients (accuracy 80.5 ± 5.6%) but that the classification parameters (channel, features and classifier) leading to the best performance varied greatly across patients. When the same channel and classifier were used for all patients (participant-generic analysis), the performance significantly decreased (accuracy 74 ± 8.3%). Significance. The present study demonstrates that to maximize the detection of brain waves across ALS patients at different stages of the disease, the classification pipeline should be tuned to each patient individually.