Influencia de los pensamientos disfuncionales en la sobrecarga de los cuidadores de personas dependientes

Vázquez‐Sánchez, María Ángeles; Aguilar-Trujillo, María Pilar; Estébanez-Carvajal, Francisca María; Casals, Cristina; Casals-Sánchez, J.L.; Heras-Pérez, María Carmen

doi:10.1016/j.enfcli.2011.07.002

Cited by 15 publications

(6 citation statements)

References 9 publications

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“…In addition, regarding dementia caregivers, the construct of dysfunctional thoughts about caregiving has been defined as rigid thoughts related to some caregiver statements such as "Having to do everything for the person they are looking after, and preferably, doing it alone" or "Not feeling bad about caring and, if that happens, not showing their feelings publicly" (Losada, Montorio, Knight, et al, 2006). This kind of thoughts has been found to be related with negative outcomes of caregivers' mental health, such as depression (McNaughton et al, 1995;Stebbins & Pakenham, 2001) or burden (Vázquez-Sánchez et al, 2012). In order to explain how cognitive factors may contribute to caregiver health, Losada, Montorio, Knight, et al (2006) adapted the cognitive-behavioral model for the explanation of caregivers' mental health problems.…”

Section: Article In Pressmentioning

confidence: 99%

Associations of knowledge about Alzheimer’s disease, dysfunctional cognition, and coping with caregiver’s blood pressure

et al. 2021

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Caring for a relative with Alzheimer's disease or related disorders has been considered to be a prototypical example of chronic stressful situations (Vitaliano et al., 2004). The main models of the caregiving stress process assume that "the onset and progression of dementia are stressful for both the patient and the caregiver" (Schulz & Sherwood, 2008, p. 2). In this sense, caregivers' health consequences are considered to be relevant for care recipients' health outcomes, as caregiver distress is associated with institutionalization, elder abuse of dementia care recipients, and worsening behavioral and psycholo-gical symptoms of dementia (Stall et al., 2019). In addition, caregivers' mental health predicts mortality of patients with neurodegenerative diseases (Lwi et al., 2017).The caring situation has also been found to be associated with negative consequences for caregivers' physical and mental health, including increased risk of developing a cardiovascular disease (Mausbach et al.

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Section: Article In Pressmentioning

confidence: 99%

Associations of knowledge about Alzheimer’s disease, dysfunctional cognition, and coping with caregiver’s blood pressure

et al. 2021

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“…Entre los cónyuges destaca también la mujer que cuida a su esposo; siendo cada vez más frecuente el varón cuidador de elevada edad 9 . Según la literatura científica revisada sobre el tema, las necesidades de las PC están condicionadas por factores propios como el género, la edad y el nivel de formación, pero también por otros como el peso de las tradiciones de cada lugar, las circunstancias culturales y los apoyos sociales y sanitarios recibidos, además de las repercusiones negativas en la salud como consecuencia del cuidado [10][11][12][13] . En estos otros factores juega un importante papel el ámbito en el que habitualmente viven.…”

Section: Escuela Universitaria De Enfermería Virgen De Lasunclassified

Influencia del ámbito, rural o urbano, en la percepción de los apoyos y las necesidades de las personas cuidadoras en el hospital

Gorlat-Sánchez

García‐Caro

Peinado-Gorlat

et al. 2013

Anales Sis San Navarra

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Fundamento. Tras implementar un Plan Funcional con medidas de apoyo a personas cuidadoras en dos hospitales de Granada, se analizan la eficacia y el efecto del medio en la percepción y las necesidades de la persona cuidadora. Material y método. Se realizó un estudio cualitativo, fenomenológico, a través de entrevistas semi-estructuradas. Participaron 45 personas cuidadoras incluidas en el Plan Funcional. Se midieron además apoyo social percibido, función familiar y nivel de ansiedad mediante los cuestionarios Duke-unc, Apgar familiar y Escala de Goldberg, respectivamente. El análisis de los datos cualitativos se llevó a cabo mediante codificación abierta, axial y selectiva, y los cuestionarios mediante estadística descriptiva. resultado. Las personas cuidadoras del ámbito urbano valoraron más los apoyos que les facilitaban la vida en el hospital y los apoyos sociales para el domicilio y las del ámbito rural los apoyos hospitalarios orientados a educación en cuidados para cuando estuviesen en su domicilio, todos ellos vinculados a la personalización de cuidados. Las alteraciones personales por el cuidado están presentes en ambos ámbitos aunque difieren en las repercusiones psíquicas y en el tipo de fármacos y su consumo. Existen diferencias en cuanto a los apoyos necesarios y las dificultades encontradas. conclusiones. El ámbito donde habitualmente viven las personas cuidadoras condiciona sus percepciones del cuidado y algunas de sus necesidades en el hospital. Se deberán revisar las medidas del Plan Funcional cuestionadas, redefinir algunas prioridades e incluir medidas adicionales en función de la situación familiar de las personas cuidadoras. Palabras clave. Dependencia. Hospitalización. Cuidadores. Zona rural. Zona urbana. aBstract Background. After the Functional Plan was implemented with support measures for caregivers in hospitals of Granada (Spain), the effectiveness and impact of environment on the perception and needs of caregivers was analysed. Materials and methods. A qualitative, phenomenological study was made through semi-structured interviews. A total of 45 caregivers included in the Functional Plan participated. In addition, perceived social support, family functioning, and the anxiety level was measured, respectively, through the Duke-UNC, Apgar Family, and Goldberg Scale questionnaires. The data were qualitatively analysed by open, axial, and selective coding, and the questionnaires by descriptive statistics. results. The caregivers of the urban setting valued more the support that made their life easier in the hospital and the social support at home, while caregivers in rural settings valued the hospital support oriented towards education in care for life after returning home, all linked to the personalization of care. The personal disturbances due to care occurred in all the settings, although differences appeared in psychic repercussions and in the type of drugs and their consumption. There were differences in terms of support needed and the difficulties encountered. conclusions. The setting...

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“…Using the DSM-IV criteria for insomnia, a prevalence of 6% has been reported, with primary insomnia being most frequently cited (2-4%), followed by insomnia related to mental disorder (1-3%) [9]. Informal caregivers of persons with dependency may experience stress and dysfunctional thoughts [10]. This is often the case of caregivers for persons with cancer, receiving home palliative care.…”

Section: Introductionmentioning

confidence: 99%

Intervention to improve quality of sleep of palliative patient carers in the community: protocol for a multicentre randomised controlled trial

Valero-Cantero¹,

Carrión-Velasco²,

Casals

et al. 2020

BMC Nurs

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Background Sleep disorders are commonly experienced by community caregivers for persons with cancer, with at least 72% reporting moderate to severe disorders. A consequence of this condition, which is associated with the presence of overload in the caregiver, is the increased risk of clinical depression. The aim of this study is to evaluate the effects of music on the sleep quality achieved by informal caregivers for cancer patients receiving home palliative care. In addition, we will assess the influence of specific variables that could modify these effects, analyse the correlates related to nocturnal wakefulness and consider the diurnal consequences according to the sleep characteristics identified. Methods This single-blind, multicentre, randomised clinical trial will focus on informal providers of care for cancer patients. Two samples of 40 caregivers will be recruited. The first, intervention, group will receive seven music-based sessions. The control group will be masked with seven sessions of therapeutic education (reinforcing previous sessions). Outcomes will be evaluated using the Pittsburgh Sleep Quality Index, a triaxial accelerometer, EuroQol-5D-5L, the Caregiver Strain Index, the Epworth Sleepiness Scale and the Client Satisfaction Questionnaire. The caregivers’ satisfaction with the intervention performed will also be examined. Discussion This study is expected to extend our understanding of the efficacy of music therapy in enhancing the sleep quality of caregivers for patients receiving home palliative care. To our knowledge, no reliable scientific investigations of this subject have previously been undertaken. Music is believed to benefit certain aspects of sleep, but this has yet to be proven and, according to a Cochrane review, high-quality research in this field is necessary. One of the main strengths of our study, which heightens the quality of the randomised clinical trial design, is the objective assessment of physical activity by accelerometry and the use of both objective and subjective measures of sleep in caregivers. Music therapy for the caregivers addressed in this study is complementary, readily applicable, provokes no harmful side effects and may produce significant benefits. Trial registration The IMECA study is registered at Clinical Trials.gov, ClinicalTrials.gov Identifier: NCT04491110. Registered 29 July, 2020.

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Influencia de los pensamientos disfuncionales en la sobrecarga de los cuidadores de personas dependientes

Cited by 15 publications

References 9 publications

Associations of knowledge about Alzheimer’s disease, dysfunctional cognition, and coping with caregiver’s blood pressure

Associations of knowledge about Alzheimer’s disease, dysfunctional cognition, and coping with caregiver’s blood pressure

Influencia del ámbito, rural o urbano, en la percepción de los apoyos y las necesidades de las personas cuidadoras en el hospital

Intervention to improve quality of sleep of palliative patient carers in the community: protocol for a multicentre randomised controlled trial

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