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5 result(s) search for keyword(s) 'Agitation.Dementia.Aromatherapy.Caregiver burden.' 
Add the result to your basket Refine your search Apply to external sources Make a suggestionEffects of arnomatherapy on agitation and related caregiver burden in / Ozdemir, Leyla in Geriatric Nursing, Vol.38 No.3 (May-Jun) 2017 ([07/31/2017])
Title : Effects of arnomatherapy on agitation and related caregiver burden in : patients with moderate to severe demintia A pilot study Material Type: printed text Authors: Ozdemir, Leyla, Author Publication Date: 2017 Article on page: p.231-237 Languages : English (eng) Original Language : English (eng)
in Geriatric Nursing > Vol.38 No.3 (May-Jun) 2017 [07/31/2017] . - p.231-237Keywords: Agitation.Dementia.Aromatherapy.Caregiver burden. Abstract: We examined the effects of aromatherapy on agitation in patients with dementia and evaluated related caregiver burden. Patients and their caregivers from two hospitals in Turkey were selected and divided into an intervention group (n = 14) and a control group (n = 14). Patients were stratified according to their dementia phase and intake of antipsychotic medication. The intervention group received aromatherapy via massage and inhalation at home for 4 weeks. The control group received no intervention. Data were collected using the Neuropsychiatric Inventory (NPI), the Cohen-Mansfield Agitation Inventory (CMAI) and the Zarit Burden Interview (ZBI). At 2 and 4 weeks, the NPI scores were significantly lower in the intervention group (p < 0.05). At 4 weeks, the CMAI and ZBI scores were significantly lower in the intervention group (p < 0.05). In conclusion, after aromatherapy, agitation, neuropsychiatric symptoms, and caregiver distress significantly reduced, and aromatherapy prevented caregiver burden increase. Link for e-copy: http://www.gnjournal.com/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27101 [article] Effects of arnomatherapy on agitation and related caregiver burden in : patients with moderate to severe demintia A pilot study [printed text] / Ozdemir, Leyla, Author . - 2017 . - p.231-237.
Languages : English (eng) Original Language : English (eng)
in Geriatric Nursing > Vol.38 No.3 (May-Jun) 2017 [07/31/2017] . - p.231-237Keywords: Agitation.Dementia.Aromatherapy.Caregiver burden. Abstract: We examined the effects of aromatherapy on agitation in patients with dementia and evaluated related caregiver burden. Patients and their caregivers from two hospitals in Turkey were selected and divided into an intervention group (n = 14) and a control group (n = 14). Patients were stratified according to their dementia phase and intake of antipsychotic medication. The intervention group received aromatherapy via massage and inhalation at home for 4 weeks. The control group received no intervention. Data were collected using the Neuropsychiatric Inventory (NPI), the Cohen-Mansfield Agitation Inventory (CMAI) and the Zarit Burden Interview (ZBI). At 2 and 4 weeks, the NPI scores were significantly lower in the intervention group (p < 0.05). At 4 weeks, the CMAI and ZBI scores were significantly lower in the intervention group (p < 0.05). In conclusion, after aromatherapy, agitation, neuropsychiatric symptoms, and caregiver distress significantly reduced, and aromatherapy prevented caregiver burden increase. Link for e-copy: http://www.gnjournal.com/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27101
Title : Caregiver burden among caregivers of individuals with severe mental illness : testing the moderation and mediation models of resillence Material Type: printed text Authors: Mulud, Zamzaliza Abdul, Author ; McCarthy, Geraldine, Author Publication Date: 2017 Article on page: p.24-30 Languages : English (eng) Original Language : English (eng)
in Archives of Psychiatric Nursing > Vol.31 No.1 (Feb) 2017 [07/20/2017] . - p.24-30Keywords: Caregiver burden.Mental illness.Moderation and Mediation models Abstract: The association between the socio-demographic characteristics of caregivers, such as gender and caregiver burden, is well documented; however, the process underlying this relationship is poorly understood. Based on the stress process model, we designed a cross-sectional study to examine the mediating and moderating effect of resilience on the relationship between gender and caregiver burden. Caregivers of individuals with severe mental illness (n = 201) were recruited in two psychiatric outpatient clinics in Malaysia. The relationship between the gender of the caregiver and caregiver burden was mediated by resilience, thus supporting the stress process model. The findings from the present research contribute to the growing evidence of the interaction between socio-demographic variables of caregivers and resilience, and caregiver burden.
Link for e-copy: http://www.psychiatricnursing.org/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27073 [article] Caregiver burden among caregivers of individuals with severe mental illness : testing the moderation and mediation models of resillence [printed text] / Mulud, Zamzaliza Abdul, Author ; McCarthy, Geraldine, Author . - 2017 . - p.24-30.
Languages : English (eng) Original Language : English (eng)
in Archives of Psychiatric Nursing > Vol.31 No.1 (Feb) 2017 [07/20/2017] . - p.24-30Keywords: Caregiver burden.Mental illness.Moderation and Mediation models Abstract: The association between the socio-demographic characteristics of caregivers, such as gender and caregiver burden, is well documented; however, the process underlying this relationship is poorly understood. Based on the stress process model, we designed a cross-sectional study to examine the mediating and moderating effect of resilience on the relationship between gender and caregiver burden. Caregivers of individuals with severe mental illness (n = 201) were recruited in two psychiatric outpatient clinics in Malaysia. The relationship between the gender of the caregiver and caregiver burden was mediated by resilience, thus supporting the stress process model. The findings from the present research contribute to the growing evidence of the interaction between socio-demographic variables of caregivers and resilience, and caregiver burden.
Link for e-copy: http://www.psychiatricnursing.org/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27073
Title : Impact of Non-medical Out-of-pocket Expenses on Families of Children : With Cerebral Palsy Following Orthopaedic Surgery Material Type: printed text Authors: Vessey Judith A., Author ; DiFazio, Rachel L., Author ; Strou, Tania D, Author ; Snyde, Brian D, Author Publication Date: 2018 Article on page: p.101-107 Languages : English (eng) Original Language : English (eng)
in Journal of Pediatric Nursing > Vol.37 No.6 (Nov-Dec) 2017 [03/29/2018] . - p.101-107Keywords: Non-medical out-of-pocket expenses, Cerebral palsy, Financial burden, Impact on Family Scale, Assessment of Caregivers Experience with Neuromuscular Disease (ACEND), Children with Special Health Care Needs. Abstract: Purpose
Limited research has been conducted on the non-medical out-of-pocket expenses (NOOPEs) incurred by families of children with chronic health conditions. The study objectives were to: 1) calculate the estimated NOOPEs incurred by families during hospitalization of their child, 2) identify predictors of high NOOPEs, and 3) assess the impact of the child's chronic health condition on the family's finances.
Design and Methods
Prospective observational study. Parents were included if their child was 3–20 years old, had severe, non-ambulatory cerebral palsy (CP), and scheduled for hip or spine surgery. Parents reported all NOOPEs incurred during their child's hospitalization using the Family Expense Diary. Families completed the subscales of the Impact on Family Scale and the Assessment of Caregivers Experience with Neuromuscular Disease. Descriptive and univariate and multiple hierarchical regression models were used in the analysis.
Results
Fifty two parents participated. The total NOOPEs ranged from $193.00 to $7192.71 (M = $2001.92) per hospitalization representing an average of 4% of the family's annual earned income. Caregiver age (F = 8.393, p < 0.001), income (F = 7.535, p < 0.001), and distance traveled to the hospital (F = 4.497, p = 0.039) were significant predictors of high NOOPEs. The subscale scores indicated that a child's chronic health condition had a significant impact on family finances.
Conclusions and Practice Implications
Hospitalization is associated with numerous NOOPEs that create additional financial demands for families caring for a child with severe CP. NOOPEs should be addressed when preparing families for their children's planned hospital admissions, especially those families of CSHCN who experience significant financial impacts secondary to their children's care.Link for e-copy: http://www.journals.elsevier.com/journal-of-pediatric-nursing/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27634 [article] Impact of Non-medical Out-of-pocket Expenses on Families of Children : With Cerebral Palsy Following Orthopaedic Surgery [printed text] / Vessey Judith A., Author ; DiFazio, Rachel L., Author ; Strou, Tania D, Author ; Snyde, Brian D, Author . - 2018 . - p.101-107.
Languages : English (eng) Original Language : English (eng)
in Journal of Pediatric Nursing > Vol.37 No.6 (Nov-Dec) 2017 [03/29/2018] . - p.101-107Keywords: Non-medical out-of-pocket expenses, Cerebral palsy, Financial burden, Impact on Family Scale, Assessment of Caregivers Experience with Neuromuscular Disease (ACEND), Children with Special Health Care Needs. Abstract: Purpose
Limited research has been conducted on the non-medical out-of-pocket expenses (NOOPEs) incurred by families of children with chronic health conditions. The study objectives were to: 1) calculate the estimated NOOPEs incurred by families during hospitalization of their child, 2) identify predictors of high NOOPEs, and 3) assess the impact of the child's chronic health condition on the family's finances.
Design and Methods
Prospective observational study. Parents were included if their child was 3–20 years old, had severe, non-ambulatory cerebral palsy (CP), and scheduled for hip or spine surgery. Parents reported all NOOPEs incurred during their child's hospitalization using the Family Expense Diary. Families completed the subscales of the Impact on Family Scale and the Assessment of Caregivers Experience with Neuromuscular Disease. Descriptive and univariate and multiple hierarchical regression models were used in the analysis.
Results
Fifty two parents participated. The total NOOPEs ranged from $193.00 to $7192.71 (M = $2001.92) per hospitalization representing an average of 4% of the family's annual earned income. Caregiver age (F = 8.393, p < 0.001), income (F = 7.535, p < 0.001), and distance traveled to the hospital (F = 4.497, p = 0.039) were significant predictors of high NOOPEs. The subscale scores indicated that a child's chronic health condition had a significant impact on family finances.
Conclusions and Practice Implications
Hospitalization is associated with numerous NOOPEs that create additional financial demands for families caring for a child with severe CP. NOOPEs should be addressed when preparing families for their children's planned hospital admissions, especially those families of CSHCN who experience significant financial impacts secondary to their children's care.Link for e-copy: http://www.journals.elsevier.com/journal-of-pediatric-nursing/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27634
Title : Psychometric Properties of the Turkish Version of Caregiver Burden Index (CBI) : for Parents of Children with Allergies Material Type: printed text Authors: Ekim, Ayfer, Author ; Hecan, Melis, Author ; Orenm Serkan, Author Publication Date: 2017 Article on page: p.78-82 Languages : English (eng) Original Language : English (eng)
in Journal of Pediatric Nursing > Vol.35 No.4 (Jul-Aug) 2017 [09/04/2017] . - p.78-82Keywords: Allergy, Caregiver burden, Child, Parent, Reliability, Validity. Abstract: Purpose
The purpose of this study was to examine the psychometric properties of the Caregiver Burden Index (CBI) in Turkish mothers of children with allergies.
Method
The participants of this methodological study were 213 mothers of children with allergies between 6 and 12 years. Construct validity was evaluated through factor analysis and reliability was evaluated through internal consistency and item-total correlation.
Results
In reliability analysis, the overall Cronbach's alpha value (0.85) demonstrated a high level of reliability. The corrected item-total correlation varied between 0.63 and 0.84. In exploratory factor analysis, it was detected that 3 factors structure explained 73.6% of the total variance.
Conclusion
This study indicated that the CBI is a valid and reliable tool to assess the caregiver burden of mothers of Turkish children with allergies.Link for e-copy: http://www.journals.elsevier.com/journal-of-pediatric-nursing/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27445 [article] Psychometric Properties of the Turkish Version of Caregiver Burden Index (CBI) : for Parents of Children with Allergies [printed text] / Ekim, Ayfer, Author ; Hecan, Melis, Author ; Orenm Serkan, Author . - 2017 . - p.78-82.
Languages : English (eng) Original Language : English (eng)
in Journal of Pediatric Nursing > Vol.35 No.4 (Jul-Aug) 2017 [09/04/2017] . - p.78-82Keywords: Allergy, Caregiver burden, Child, Parent, Reliability, Validity. Abstract: Purpose
The purpose of this study was to examine the psychometric properties of the Caregiver Burden Index (CBI) in Turkish mothers of children with allergies.
Method
The participants of this methodological study were 213 mothers of children with allergies between 6 and 12 years. Construct validity was evaluated through factor analysis and reliability was evaluated through internal consistency and item-total correlation.
Results
In reliability analysis, the overall Cronbach's alpha value (0.85) demonstrated a high level of reliability. The corrected item-total correlation varied between 0.63 and 0.84. In exploratory factor analysis, it was detected that 3 factors structure explained 73.6% of the total variance.
Conclusion
This study indicated that the CBI is a valid and reliable tool to assess the caregiver burden of mothers of Turkish children with allergies.Link for e-copy: http://www.journals.elsevier.com/journal-of-pediatric-nursing/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27445
Title : Relationship Between Caregiving Burden and Anger Level in Primary Caregivers of Individuals With Chronic Mental Illness Material Type: printed text Authors: Bademl, Kerime, Author ; Lök, Neslihan, Author Publication Date: 2017 Article on page: p.263-268 General note: •It found that caregiving burden and anger are correlated.
•Individuals who provide care to schizophrenic patients experience continuous anger in addition to their developmental, physical, social and emotional burden.
•It was determined that caregivers who were single, male, had been providing care for 1–5 years and literate had higher levels of continuous anger.Languages : English (eng) Original Language : English (eng)
in Archives of Psychiatric Nursing > Vol.31 No.3 (Jun) 2017 [10/11/2017] . - p.263-268Keywords: Anger, Burden, Schizophrenia, Caregiver Abstract: OBJECTIVES
The objective of this study was answer to the question: to what extent are the anger of the caregivers of patients diagnosed with schizophrenia and their perceived level of burden are related?
METHOD
The study is a descriptive and correlational study. The information form prepared by the researchers which questions the socio-demographic information of the individuals along with the “Caregiving Burden Inventory” which examines the burden of the caregiver as well as “Trait Anger and Anger Expression Style Scale (TAAES)” which determines the anger levels of the caregivers were used.
RESULTS
The caregiving burdens of the caregivers according to the score averages were determined as 11.88 ± 9.78 for time and dependency burden, 11.93 ± 8.46 for developmental burden, 8.47 ± 6.63 for physical burden, 5.61 ± 5.26 for social burden, 6.29 ± 5.25 for emotional burden and the total burden score was determined as 44.19 ± 26.75. According to the trait anger and anger expression style scale score averages; trait anger was determined as 15.12 ± 5.95, anger expression as 9.70 ± 3.43, anger-in as 15.22 ± 4.02, anger control as 28.05 ± 5.57 and anger total score average as 68.11 ± 9.97.
CONCLUSION
According to the results obtained from this study, caregivers of schizophrenia patients experience developmental, physical, social and emotional burdens in addition to trait anger. The caregivers of schizophrenia patients need knowledge and support in order to control the burden and the anger they experience during the caregiving process.Link for e-copy: http://www.psychiatricnursing.org/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27352 [article] Relationship Between Caregiving Burden and Anger Level in Primary Caregivers of Individuals With Chronic Mental Illness [printed text] / Bademl, Kerime, Author ; Lök, Neslihan, Author . - 2017 . - p.263-268.
•It found that caregiving burden and anger are correlated.
•Individuals who provide care to schizophrenic patients experience continuous anger in addition to their developmental, physical, social and emotional burden.
•It was determined that caregivers who were single, male, had been providing care for 1–5 years and literate had higher levels of continuous anger.
Languages : English (eng) Original Language : English (eng)
in Archives of Psychiatric Nursing > Vol.31 No.3 (Jun) 2017 [10/11/2017] . - p.263-268Keywords: Anger, Burden, Schizophrenia, Caregiver Abstract: OBJECTIVES
The objective of this study was answer to the question: to what extent are the anger of the caregivers of patients diagnosed with schizophrenia and their perceived level of burden are related?
METHOD
The study is a descriptive and correlational study. The information form prepared by the researchers which questions the socio-demographic information of the individuals along with the “Caregiving Burden Inventory” which examines the burden of the caregiver as well as “Trait Anger and Anger Expression Style Scale (TAAES)” which determines the anger levels of the caregivers were used.
RESULTS
The caregiving burdens of the caregivers according to the score averages were determined as 11.88 ± 9.78 for time and dependency burden, 11.93 ± 8.46 for developmental burden, 8.47 ± 6.63 for physical burden, 5.61 ± 5.26 for social burden, 6.29 ± 5.25 for emotional burden and the total burden score was determined as 44.19 ± 26.75. According to the trait anger and anger expression style scale score averages; trait anger was determined as 15.12 ± 5.95, anger expression as 9.70 ± 3.43, anger-in as 15.22 ± 4.02, anger control as 28.05 ± 5.57 and anger total score average as 68.11 ± 9.97.
CONCLUSION
According to the results obtained from this study, caregivers of schizophrenia patients experience developmental, physical, social and emotional burdens in addition to trait anger. The caregivers of schizophrenia patients need knowledge and support in order to control the burden and the anger they experience during the caregiving process.Link for e-copy: http://www.psychiatricnursing.org/ Record link: http://libsearch.siu.ac.th/siu/opac_css/index.php?lvl=notice_display&id=27352
