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1.
Disabil Rehabil ; 44(15): 4004-4013, 2022 07.
Artigo em Inglês | MEDLINE | ID: mdl-33605171

RESUMO

PURPOSE: To identify healthcare professionals' perspectives on key barriers to improving physical activity in hospitalized adult patients, and to identify solutions to overcome these barriers. METHODS: We used an explanatory sequential mixed-methods study design in a Dutch university hospital. A survey exploring 39 potential barriers was completed by 15 physicians/physician assistants, 106 nurses, four nursing assistants, and four physical therapists working on surgery, internal medicine, and cardiology wards. Next, three in-depth semi-structured focus groups - comprising 30 healthcare professionals - discussed the survey findings to identify key barriers and solutions. Focus group discussions were analyzed using thematic analysis. RESULTS: Five themes were identified that described both the key barriers and the solutions to overcome these barriers. Healthcare professionals proposed several solutions, including clarifying the definition of physical activity, empowering patients to take responsibility for physical activity, giving physical therapists or physicians a prominent role in encouraging physical activity, and changing the hospital ward to entice patients to become physically active. CONCLUSIONS: Healthcare professionals need clear guidelines, roles, and responsibilities when it comes to physical activity. They also need personalized interventions that empower patients in physical activity. Finally, hospital wards should be designed and furnished so that patients are encouraged to be active.IMPLICATIONS FOR REHABILITATIONMany healthcare professionals want to sustainably improve physical activity in hospitalized adults.For this they need clear guidelines that not only define physical activity, but also describe the roles and responsibilities of all members of the medical team.Healthcare professionals need interventions that help to empower patients to take an active role in physical activity during hospital stay.Hospital wards should be designed and furnished so that patients are encouraged to be physically active.


Assuntos
Exercício Físico , Fisioterapeutas , Adulto , Atenção à Saúde , Grupos Focais , Humanos , Tempo de Internação , Pesquisa Qualitativa
2.
J Neurol Neurosurg Psychiatry ; 87(7): 775-81, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26341327

RESUMO

OBJECTIVE: To examine the longitudinal associations between caregiver strain and patients' clinical and psychosocial characteristics as well as caregivers' psychosocial characteristics. METHODS: At 4-month intervals during the 12 months study period, longitudinal data on caregiver strain and patient and caregiver factors potentially associated with caregiver strain were collected from 126 couples, who participated in a randomised controlled trial on the effectiveness of case management in amyotrophic lateral sclerosis (ALS). Caregiver strain was assessed with the Caregiver Strain Index (CSI). Patient and caregiver factors included sociodemographic characteristics, distress, coping style and perceived quality of care, as well as the patient's functional status and emotional functioning. Multilevel regression analyses were performed. RESULTS: Caregiver strain increased significantly during the study period (ß=0.315 points/months, p<0.001) and was significantly associated with patient time-dependent factors functional status (ß=-0.131 points/months, p<0.001) and emotional functioning (ß=0.022 points/months, p=0.03), and caregiver time-dependent factors passive coping style (ß=0.152 points/months, p=0.03), symptoms of anxiety (ß=0.186 points/months, p<0.001) and perceived quality of care for the caregiver (ß=-0.452 points/months, p<0.001). CONCLUSIONS: Our study has identified that apart from the patient's physical disability and emotional well-being, a passive coping style of the caregiver, increased symptoms of anxiety and feeling less supported by the ALS-team impact on caregiver strain. The multidisciplinary teams involved with the care of patients with ALS need to be aware of these factors and increase their attention for the caregiver. This will help guide the development of evidence-based supportive interventions that focus on caregiver's coping style and avoiding distress. TRIAL REGISTRATION NUMBER: Netherlands Trial Register, number NTR1270.


Assuntos
Esclerose Lateral Amiotrófica/psicologia , Esclerose Lateral Amiotrófica/terapia , Cuidadores/psicologia , Administração de Caso , Efeitos Psicossociais da Doença , Estresse Psicológico/psicologia , Adaptação Psicológica , Idoso , Ansiedade/diagnóstico , Ansiedade/psicologia , Estudos de Coortes , Feminino , Humanos , Comunicação Interdisciplinar , Colaboração Intersetorial , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Qualidade da Assistência à Saúde , Estresse Psicológico/diagnóstico
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