Objective: Evaluate the effectiveness of an intervention to family caregivers.
Design: Quasi-experimental study of type before/after, without control group.
Setting: Primary care; 5 primary care centers of Castelló city.
Period: Between the month of January 2018 and the month of January 2019.
Participants: 72 family caregivers, participants in a specific intervention recently implemented in the Department de Salut de Castelló.
Intervention: Training to family caregivers, seeking to improve knowledge of dependent care, and provide support. Ten group sessions of 120minutes.
Principal Measurements: Descriptive of sociodemographic data. Comparison of the variables overload, low back pain, social support and health-related quality of life before-after the intervention. Variable response: caregiver overload. Bivariate and multivariate analysis.
Results: All family caregivers had baseline overload (59.93±14.71); 73.3% showed low back pain, with an average level of 5.13±2.56 and moderate disability (41.7%). 50% received little social support and a great impact on health-related quality of life, especially in terms of pain and anxiety. After the intervention, there was a significant improvement (P=.004) in social support, as well as positive descriptive changes in disability due to low back pain and health-related quality of life dimensions. No progress was found (P>.05) for the presence and level of low back pain, as well as overload levels.
Conclusions: The resulting effective intervention to improve perceived social support. However, the low impact on other variables suggests reconsidering its contents, as well as encouraging new prospective studies that may offer more encouraging results.
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http://dx.doi.org/10.1016/j.aprim.2020.06.011 | DOI Listing |
Spec Care Dentist
January 2025
Cerebral Palsy Alliance Research Institute, Specialty of Child & Adolescent Health, Sydney Medical School, Faculty of Medicine & Health, The University of Sydney, Sydney, Australia.
Aims: To investigate caregiver-reported dental care experiences and oral health-related quality of life (OHRQoL) of children and young people with cerebral palsy (CP).
Methods: Between May and August 2023, caregivers of children and young people from three Australian states were invited to complete questionnaires, including the Child Oral Health Impact Profile (COHIP-SF 19).
Results: Sixty-eight caregivers participated in the survey.
Int J Eat Disord
January 2025
Faculty of Social Work, University of Calgary, Calgary, Canada.
Introduction: Studies have shown that early weight gain in family-based treatment (FBT) predicts treatment response in adolescents with anorexia nervosa (AN); however, research examining factors associated with early weight gain in FBT is limited. This study tested the feasibility and acceptability of ecological momentary assessment (EMA) in early FBT, particularly to capture momentary data on family climate during mealtimes.
Methods: Using multiple methods, quantitative (EMA) and qualitative (interviews) data were collected in the first 4 weeks of FBT.
Health Qual Life Outcomes
January 2025
Department of Human Sciences, LUMSA University, Rome, 00193, Italy.
Background: The number of people living with congenital heart disease (CHD) in 2017 was estimated to be 12 million, which was 19% higher than that in 1990. However, their death rate declined by 35%, emphasizing the importance of monitoring their quality of life due to its impact on several patient outcomes. The main objective of this study is to analyze how parents' psychosocial factors contribute to children's and adolescents' perceptions of their QoL, focusing on their medical condition.
View Article and Find Full Text PDFBMC Health Serv Res
January 2025
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine,, School of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
The primary objective of this study was to perform a psychometric evaluation of the Persian adaptation of the Assessment of Interprofessional Team Collaboration Scale (P-AITCS-II). This methodological study aimed to assess the validity and reliability of the AITCS-II for practitioners within the Iranian healthcare context. Data were collected from a sample of 230 Iranian healthcare providers between May and June 2024.
View Article and Find Full Text PDFBMC Public Health
January 2025
School of Nursing and Midwifery, Queen's University Belfast, Belfast, Northern Ireland, UK.
Background: Stigma significantly impacts individuals with Parkinson's disease (PD) and their caregivers, exacerbating social isolation, psychological distress, and reducing quality of life (QoL). Although considerable research has been conducted on PD's clinical aspects, the social and emotional challenges, like stigma, remain underexplored. Addressing stigma is crucial for enhancing well-being, fostering inclusivity and improving access to care and support.
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