Littérature scientifique sur le sujet « Maladies neurodégénératives – Psychologie »
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Articles de revues sur le sujet "Maladies neurodégénératives – Psychologie"
Lallemant, Maxime, et Marie-Frédérique Bacqué. « Accompagner les aidants d’un proche atteint d’une maladie neurologique évolutive : les plateformes d’accompagnement et de répit en France ». Études sur la mort 160, no 2 (6 février 2024) : 137–52. http://dx.doi.org/10.3917/eslm.160.0137.
Texte intégralde Mijolla-Mellor, Sophie. « Le désarroi face à l’apparition des symptômes ». Topique 150, no 3 (2 décembre 2020) : 53–66. http://dx.doi.org/10.3917/top.150.0055.
Texte intégralBrocq, H., A. Liarte, M. H. Soriani et C. Desnuelle. « Subjectivité, décision et maladies neurodégénératives : réflexions sur la place du psychologue clinicien dans le processus décisionnel ». Revue Neurologique 169, no 6-7 (juin 2013) : 485–89. http://dx.doi.org/10.1016/j.neurol.2012.10.009.
Texte intégralBatselé, Élise, Hélène Geurts, Elise Buchet, Marie-Claire Haelewyck et Mathilde Boutiflat. « Maladie de Parkinson et besoins en matière d’outils technologiques de soutien à la communication : étude qualitative ». L’Année psychologique Vol. 124, no 1 (11 mars 2024) : 79–100. http://dx.doi.org/10.3917/anpsy1.241.0079.
Texte intégralLardenois, Olivier, Jérémy Besnard et Philippe Allain. « Théorie de l’esprit et maladies neurodégénératives corticales : profils de déficits et conséquences fonctionnelles ». Revue de neuropsychologie Volume 9, no 3 (6 octobre 2017) : 163–77. http://dx.doi.org/10.1684/nrp.2017.0428.
Texte intégralHahn-Barma, V. « L'évaluation neuropsychologique dans le cadre des démences neurodégénératives. Illustration avec la maladie d'Alzheimer ». Pratiques Psychologiques 11, no 4 (décembre 2005) : 307–17. http://dx.doi.org/10.1016/j.prps.2005.09.003.
Texte intégralLardenois, Olivier, Jérémy Besnard et Philippe Allain. « Théorie de l’esprit et maladies neurodégénératives sous-corticales : profils de déficits et conséquences fonctionnelles ». Revue de neuropsychologie Volume 10, no 2 (19 juin 2018) : 121–29. http://dx.doi.org/10.1684/nrp.2018.0457.
Texte intégralTandetnik, Caroline, Thierry Hergueta, Velina Negovanska, Bruno Dubois et Catherine Bungener. « Traduction française du « Dysfunctional Thoughts about Caregiving Questionnaire-DTCQ ». Étude préliminaire auprès d’aidants de personnes atteintes de maladies neurodégénératives ». Journal de Thérapie Comportementale et Cognitive 24, no 1 (mars 2014) : 5–13. http://dx.doi.org/10.1016/j.jtcc.2013.11.001.
Texte intégralLeu-Semenescu, S. « Sommeil et maladies neurodégénératives ». Médecine du Sommeil, novembre 2022. http://dx.doi.org/10.1016/j.msom.2022.10.004.
Texte intégralThèses sur le sujet "Maladies neurodégénératives – Psychologie"
Delgadillo, Iniguez Luis Daniel. « Troubles de la Motivation et Maladies Neurovégétatives : l'Apathie dans la maladie de Parkinson et la Sclérose Latérale Amyotrophique ». Montpellier 3, 2007. http://www.theses.fr/2007MON30042.
Texte intégralApathy is a motivation disorder that has an important influence in the emotional domain. Studies published concerning the relationship between apathy and cognitive and emotional disorders are not exhaustive. No comparisons have been established according to the different kinds of neurological diseases. The objective of this study is to demonstrate the heterogeneity of the apathetic syndrome and it’s mechanisms in different progressive neurological diseases (Parkinson’s disease and Amyotrophic Lateral Sclerosis (ALS) and to analyze the relationship between apathy and cognitive and emotional disturbances. We also studied the motivation disturbances using a new scale developed by Derouesné et al. (2004) that allowed a qualitative analysis of motivation. The results agree with previous studies and showed the heterogeneity of apathy in the two studies diseases. This heterogeneity is explained by the relationship of the apathy with the emotional data but not by the cognitive data. The qualitative analysis of the motivation allowed a better understanding of the apathy mechanisms and showed that patients with Parkinson’s disease attribute their reduction of activity to a real lack of motivation and ALS patients to the motor handicap induced by the disease
Manceau, Charlotte. « Analyse des dynamiques et processus dyadiques sous-jacents à l'expérience du couple confronté à une maladie neuroévolutive ». Electronic Thesis or Diss., Université de Lille (2022-....), 2024. https://pepite-depot.univ-lille.fr/ToutIDP/EDSHS/2024/2024ULILH020.pdf.
Texte intégralNeurodegenerative diseases (NDDs) raise numerous implications for the health, well-being, and quality of life of both the partner with the disease and their caregiving spouses. In the face of these challenges, numerous studies have sought to understand the experiences of these individuals and evaluate the effectiveness of well-being-centered interventions. While individual approaches are important, the literature has underscored the significance of considering the dyad and the relational processes at play, particularly to optimize such interventions. However, while numerous models detail how couples adjust to chronic illness, NDDs are not integrated into these models, except for a few exceptions, indicating the need for further investigation of couple functioning in the context of NDDs. Therefore, the objectives of this thesis were to better understand the experiences of couples and the dyadic processes underlying their functioning, through a meta-synthesis centered on various NDDs (study 1) and two studies and functioning of couples facing Parkinson's disease (PD) (studies 2 and 3). Capturing changes in couple functioning across different stages of the disease was another objective. A thematic synthesis (study 1) and two qualitative empirical studies using Interpretative Phenomenological Analysis (study 2) were conducted. Study 2 explored the experiences of 15 couples at the specific stage known as the honeymoon period of PD. Study 3 involved a comparison of processes identified in three distinct samples of 15 couples, at three stages of PD, to identify prevalent functioning patterns and transitions in couple dynamics throughout the disease progression. Studies 2 and 3 identified five patterns of dyadic functioning, as well as transitions in dyadic dynamics, often linked to symptom progression. Some partners demonstrate mutual support and positive reinterpretation of their experience, evolving towards a dynamic where the caregiver provides subtle assistance to preserve this balance. For others, this discreet help, a subject of negotiation within the couple from the onset of the disease, abruptly transforms into control. While some spouses struggle against the disease from the early stages by exerting a form of control, their partner disengages. With symptom progression, it becomes impossible to avoid this control, which turns into intrusion. Additionally, some couples adopt a rigid hyperprotection against the distress induced by PD, with this avoidance strengthening over time. Finally, another pattern, characterized by difficulty in understanding the other's perspective and by a mutual disengagement shown by partners, also becomes more rigid over time, potentially leading to questioning the couple's relationship. These studies have highlighted different dyadic dynamics and their associated processes within the context of NDDs, specifically PD. The transitions identified in couple functioning throughout the disease progression indicate the importance of considering the couple's experience from the onset of the disease and throughout its evolution. These findings are significant, as they suggest several specificities of dyadic functioning in the face of NDDs. Furthermore, they reveal similarities in processes observed in the context of PD, Alzheimer's disease, or other chronic illnesses. These various aspects are thus important for the development of transdiagnostic interventions and future research aimed at exploring dyadic processes associated with couples' experience of other less studied diseases
Piquard, Ambre. « Attention préparatoire et attention sélective : étude et relations avec la planification et les activités de la vie quotidienne chez des patients présentant une maladie neurodégénérative responsable d'un dysfonctionnement frontal ». Paris 5, 2003. http://www.theses.fr/2003PA05H018.
Texte intégralAttention is essential for mental functioning (in individuals) because of its implication in behavioural regulation and adaptation. LaBerge (1995) proposed a model of attention including the notion of preparatory attention, in which the frontal lobes seem to play a crucial role. Preparatory attention contributes to goal achievement and, more generally, to adaptative behavior. We studied preparatory attention, using an experimental test developed by LaBerge (LaBerge et al. , 2000) in patients suffering from a neurodegenerative disease involving frontal lobe dysfunction (frontotemporal dementia associated or not with amyotrophic lateral sclerosis, Alzheimer's disease, Parkinson's disease) in which attentional defecits are frequently described. The results are in contradiction to precedent studies. The slope of response times, measure of preparatory attention proposed by LaBerge, could reflect different processes depending on whether this slope is high or low. The study of the orientation of selective attention using the spatial cueing task (Posner, 1980) demonstrates an engagement and/or disengagement deficit associated with an inhibition of return deficit in patients with FTD and AD. We also studied the implication of preparatory attention in planning and activities of daily living. The relationship with planning and activities of daily living confirms the necessity to dissociate both types of slope in so far as only low slopes are correlated with these activities. The low slopes may potentially be the reflection of a deficit in working memory, global attention or divided attention. Our results confirm the implication of an attentional component in planning and activities. However, preparatory attention does not seem to be linked specifically to these activities
Vendette, Mélanie. « Étude de la perfusion cérébrale régionale dans le trouble comportemental en sommeil paradoxal ». Thèse, 2012. http://hdl.handle.net/1866/10123.
Texte intégralRapid eye movement sleep behavior disorder (RBD) is a parasomnia characterized by intermittent loss of normal atonia during REM sleep and elaborate motor activity associated with dreams. RBD may occur in an idiopathic form (iRBD), but is frequent in neurodegenerative diseases characterized by alpha-synuclein deposition such as Parkinson’s disease (PD) and dementia with Lewy bodjes (DLB). Biomarkers of synucleinopathies, such as motor, olfaction and color discrimination dysfunctions have been found in patients with iRBD. Moreover, impaired cerebral activities with neuroimaging and cognitive perturbations have also been detected in those patients. Longitudinal studies have demonstrated that iRBD might precede PD or DLB by several years. This suggests that iRBD could represent a risk factor of synucleinopathies. The goal of the present research was to investigate the resting regional cerebral blood flow (rCBF) in an iRBD sample using single photon emission computerized tomography (SPECT) neuroimaging. This led to two different studies. The aim of the first study was to compare the rCBF between a group of patients with iRBD and a group of healthy control subjects, and to explore correlations between rCBF of iRBD patients and markers of synucleinopathies. The results of this study showed that compared to controls, iRBD patients had decreased perfusion in frontal and parietal cortical regions and an increased perfusion in pons, putamen and hippocampus bilaterally. Moreover, a significant correlation between brain perfusion in frontal and occipital cortex and performance on a color discrimination test was found in iRBD patients. The brain perfusion anomalies observed in our iRBD patients are similar to those observed in PD in functional neuroimaging studies, suggesting similar neuroanatomic basis between these two pathologies. The objective of the second study was to investigate brain perfusion changes associated with mild cognitive impairment (MCI) in iRBD. We compared rCBF of a sub-group of patients with iRBD and MCI, a sub-group of patients with iRBD without MCI and a group of healthy control subjects. The results showed that only iRBD with MCI showed decreased perfusion in posterior brain regions, in occipital and temporo-parietal areas. These anomalies found in iRBD with MCI are similar to those reported in other studies in PD patients with dementia (PDD) and DLB in neuroimaging studies. To conclude, the results of this research showed brain perfusion abnormalities in iRBD patients similar to those found in synucleinopathies. One of our studies demonstrated a specific pattern of cerebral anomalies with SPECT, similar to those found in PDD and DLB, in patients with iRBD and MCI compared to iRBD without MCI. These biomarkers of synucleinopathies in iRBD suggest that these patients might be at higher risk to develop a neurodegenerative disease associated with alpha synuclein deposition.
Rodrigues, Brazète Jessica. « Marqueurs électroencéphalographiques du développement d’une maladie neurodégénérative dans le trouble comportemental en sommeil paradoxal ». Thèse, 2015. http://hdl.handle.net/1866/13748.
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