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1.
BMC Public Health ; 22(1): 1910, 2022 10 13.
Artigo em Inglês | MEDLINE | ID: mdl-36229815

RESUMO

BACKGROUND: This study aimed to capture public beliefs about living with obesity, examine how these beliefs have changed over time and to explore whether certain characteristics were associated with them in a nationally representative sample of adults from the Republic of Ireland (RoI) and Northern Ireland (NI). METHODS: A cross-sectional survey employed a random quota sampling approach to recruit a nationally representative sample of 1046 adults across NI and RoI. Telephone interviews captured information on demographics; health behaviours & attitudes; and beliefs about the consequences of obesity (measured using the Obesity Beliefs Scale). Univariable analyses compared beliefs about the consequences of living with obesity between participants with a self-reported healthy weight and those living with overweight or obesity, and non-responders (those for whom weight status could not be ascertained due to missing data). Multiple linear regression examined associations between obesity-related beliefs and socio-demographics, self-rated health and perceived ability to change health behaviours. Multiple linear regression also compared changes in obesity-related beliefs between 2013 and 2020 in the RoI. RESULTS: Higher endorsement of the negative outcomes of obesity was significantly associated with living with a healthy weight, higher self-rated health, dietary quality and perceived ability to improve diet and physical activity. Those who lived with overweight, with obesity and non-responders were less likely to endorse the negative consequences of obesity. Those living with obesity and non-responders were also more likely to support there is an increased cost and effort in maintaining a healthy weight. Comparison with survey data from 2013 showed that currently, there is a greater endorsement of the health benefits of maintaining a healthy weight (p < 0001), but also of the increased costs associated with it (p < 0001). CONCLUSION: Beliefs about the consequences of maintaining a healthy body weight are associated with individuals' weight, self-rated health, diet and perceived ease of adoption of dietary and exercise-related improvements. Beliefs about the health risks of obesity and perceived greater costs associated with maintaining a healthy weight appear to have strengthened over time. Present findings are pertinent to researchers and policy makers involved in the design and framing of interventions to address obesity.


Assuntos
Obesidade , Sobrepeso , Adulto , Estudos Transversais , Dieta , Humanos , Irlanda do Norte/epidemiologia , Obesidade/epidemiologia
2.
Child Care Health Dev ; 43(1): 144-151, 2017 01.
Artigo em Inglês | MEDLINE | ID: mdl-27678488

RESUMO

BACKGROUND: The numbers of children with long-term illnesses surviving into adulthood and transferring from child to adult services has increased dramatically in the last 30 years. This study aimed to examine health-related quality of life pre- and post-transfer from child to adult healthcare for young people with three long-term illnesses. METHODS: A total of 217 young people with cystic fibrosis, congenital heart defects or diabetes attending child and adult hospital services in Dublin, Ireland completed a questionnaire survey. Multiple linear regression was used to identify predictors of five dimensions of health-related quality of life pre- and post-transfer. RESULTS: Post-transfer young people with congenital heart disease and diabetes reported significantly lower physical well-being than their pre-transfer counterparts. Pre-transfer young people with cystic fibrosis reported significantly lower physical well-being than those with diabetes, but there was no significant difference post-transfer. Pre-transfer females reported lower scores than males on the Psychological Well-being and Autonomy and Parent Relation dimensions; however, these differences disappeared post-transfer. Higher maternal overprotection scores were associated with significantly lower scores on the Psychological Well-being, Autonomy and Parent Relation, and Social Support and Peers dimensions, regardless of transfer status. CONCLUSIONS: Disease group, gender and maternal overprotection were predictors of health-related quality of life pre- and post-transfer from child to adult healthcare. Transition programmes should promote self-management and discourage parental overprotection.


Assuntos
Doença Crônica/reabilitação , Qualidade de Vida , Transição para Assistência do Adulto , Adolescente , Criança , Proteção da Criança , Doença Crônica/psicologia , Estudos Transversais , Fibrose Cística/psicologia , Fibrose Cística/reabilitação , Diabetes Mellitus Tipo 1/psicologia , Diabetes Mellitus Tipo 1/reabilitação , Feminino , Cardiopatias Congênitas/psicologia , Cardiopatias Congênitas/reabilitação , Humanos , Irlanda , Masculino , Relações Mãe-Filho , Mães/psicologia , Poder Familiar/psicologia , Autonomia Pessoal , Psicometria , Fatores Sexuais , Adulto Jovem
3.
J Cyst Fibros ; 15(4): 436-42, 2016 07.
Artigo em Inglês | MEDLINE | ID: mdl-26708264

RESUMO

BACKGROUND: The Republic of Ireland has one of the highest reported incidences of cystic fibrosis (CF) in the world (1/1353) with an estimated carrier rate of 1/20. No cure exists, however there have been significant advances in available treatments. Newborn bloodspot screening (NBS) for CF was added to the NBS programme in Ireland in July 2011. Little is known about antenatal or postnatal women's knowledge about CF. METHODS: This was a cross-sectional study of 662 antenatal (≥36weeks gestation) and 480 postnatal women (post NBS). Women were asked to self-complete a questionnaire including 14 CF knowledge questions. RESULTS: Among the respondents significantly more postnatal than antenatal women were aware that CF is included on the NBS (81.8% vs 63.5%; p<0.001). 92.7% believe that there are health consequences to being a carrier and 33.6% believe there is a cure for CF. In the multivariate analysis, lower educational status (OR 2.13; 95% CI 1.31, 3.46) being an antenatal mother (OR 1.51; 95% CI 1.04, 2.18), having no family history of CF (OR 5.82; 95% CI 1.62, 20.90) were associated with poor CF knowledge, while increasing age was found to be protective against poor CF knowledge (OR 0.96; 95% CI 0.92, 0.99). CONCLUSIONS: Results from this study provide a useful insight into women's preexisting knowledge about CF, which could be used to inform initial discussions with parents about their child's diagnosis.


Assuntos
Regulador de Condutância Transmembrana em Fibrose Cística/genética , Fibrose Cística , Letramento em Saúde , Triagem Neonatal , Assistência Perinatal , Adulto , Estudos Transversais , Fibrose Cística/diagnóstico , Fibrose Cística/epidemiologia , Fibrose Cística/genética , Fibrose Cística/psicologia , Escolaridade , Feminino , Testes Genéticos/métodos , Conhecimentos, Atitudes e Prática em Saúde , Letramento em Saúde/métodos , Letramento em Saúde/estatística & dados numéricos , Humanos , Recém-Nascido , Irlanda/epidemiologia , Anamnese , Avaliação das Necessidades , Triagem Neonatal/métodos , Triagem Neonatal/psicologia , Assistência Perinatal/métodos , Assistência Perinatal/organização & administração , Gravidez , Inquéritos e Questionários
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