2007
DOI: 10.1111/j.1365-2702.2006.01754.x
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Changing needs of Chinese family caregivers of stroke survivors

Abstract: Ongoing need assessment by nurses who are in regular contact with caregivers in hospital and community will enable appropriate interventions such as providing education and emotional support both before and after discharge to be offered to Chinese communities.

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Cited by 36 publications
(48 citation statements)
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“…None of the studies assessed the sample size a priori or reported confidence intervals. Seven studies achieved a response rate above 60%, 72, 7476, 78, 79, 81 six utilized reliable and valid measurements, 74, 7781 and seven assessed statistical significance. 72, 74, 7680 All mixed-methods studies appraised using MMAT used the methodology appropriately, used relevant sources to collect the qualitative and quantitative data, and had sample representing the population.…”
Section: Resultsmentioning
confidence: 99%
“…None of the studies assessed the sample size a priori or reported confidence intervals. Seven studies achieved a response rate above 60%, 72, 7476, 78, 79, 81 six utilized reliable and valid measurements, 74, 7781 and seven assessed statistical significance. 72, 74, 7680 All mixed-methods studies appraised using MMAT used the methodology appropriately, used relevant sources to collect the qualitative and quantitative data, and had sample representing the population.…”
Section: Resultsmentioning
confidence: 99%
“…Caregivers' support needs can be viewed as a spectrum of needs, including practical, spiritual, psychosocial, informational, emotional, and physical support needs, as adapted from the supportive care needs framework model for caregivers of cancer patients (Fitch, 1994). A number of studies have shown that the need for information is a top priority among caregivers of persons with dementia (Muangpaisan et al, 2010;Wackerbarth & Johnson, 2002), stroke (Hare, Rogers, Lester, McManus, & Mant, 2006;Kim & Moon, 2007;MacIsaac, Harrison, & Godfrey, 2010;Mak, Mackenzie, & Lui, 2007;), spinal cord injury (SCI; Meade, Taylor, Kreutzer, Marwitz, & Thomas, 2004;Post, Bloemen, & de Witte, 2005), traumatic brain injury (TBI; Arango-Lasprilla et al, 2010;Blake, 2008, Rotundi, Sinkule, & Spring, 2005Sander, Clark, Atchison, & Rueda, 2009), Parkinson's disease (PD; Hasson et al, 2010;Kristjanson, Aoun, & Oldham, 2006;Thomas & Sweetnam, 2002), and multiple sclerosis (MS; Corry & While, 2009;Kersten et al, 2000;Koopman, Benbow, & Vandervoort, 2006;Kristjanson et al, 2006). In general, caregivers of persons with chronic disease have been shown to desire two types of information: general information about the medical condition of the care recipient and specific, understandable information tailored to their situation.…”
Section: Introductionmentioning
confidence: 98%
“…Over 20% of services reported that they did not provide information about risk factor awareness and secondary prevention, which is of concern as it is particularly important that community-based clients receive information about these topics. 10,11,14,15,17,18 …”
Section: Content Of Information Provisionmentioning
confidence: 99%
“…[9][10][11][12][13][14] This mix of information needs typically continues into the chronic or community-based stage of living with the consequences of stroke. [15][16][17][18] A fear of recurrence of stroke and the subsequent need for information regarding secondary prevention is particularly strong for community-based clients with stroke and their carers.…”
mentioning
confidence: 99%
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