A New Scale to Measure Family Members' Perception of Community Health Care Services for Persons with Huntington Disease
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Summary
Findings from this study provide evidence of both construct validity and internal consistency reliability of the CHCS scale, and further psychometric testing of the scale in other samples of family caregivers of persons with HD is warranted.
- Type
- article
- Published
- 2010-03-11
- Cited by
- 4
- References
- 39
- Access
- Open access
- OpenAlex
- https://openalex.org/W1995948738
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:205333667
Keywords
Cronbach's alpha, Exploratory factor analysis, Varimax rotation, Clinical psychology, Scale (ratio)
References
- Effects of Social Support and Coping of Family Caregivers of Older Adults with Dementia in Taiwan
- “No one else sees the difference: ”family members' perceptions of changes in persons with preclinical Huntington disease
- Data analysis & statistics for nursing research
- Alzheimer's disease and the psychosocial burden for caregivers.
- Using Multivariate Statistics
- Supportive care needs of people with brain tumours and their carers
- Measurement in Nursing and Health Research
- The Practice of Nursing Research: Conduct, Critique and Utilization
- Mail and telephone surveys : the total design method
- Applied Multivariate Statistics for the Social Sciences
- Focus on psychometrics. Aspects of item analysis.
- Partners of mutation-carriers for Huntington's disease: forgotten persons?
- Caregiver burden in Huntington's disease.
- Multivariate Data Analysis
- Grief reactions and depression in caregivers of individuals with Alzheimer's disease: results from a pilot study in an urban setting.
- Stressors, social support, depressive symptoms and general health status of Taiwanese caregivers of persons with stroke or Alzheimer's disease.
- Determination and quantification of content validity.
- The Huntington’s Disease quality of life battery for carers: reliability and validity
- A framework for the study of self- and family management of chronic conditions.
- Exploration of the effects of predictive testing for Huntington disease on intimate relationships.
Cited by
- Healthcare experiences of families affected by Huntington disease: need for improved care
- Quality of Life in Huntington's Disease: Critique and Recommendations for Measures Assessing Patient Health‐Related Quality of Life and Caregiver Quality of Life
- Development of the Huntington Disease Family Concerns and Strategies Survey From Focus Group Data
- Use of the self- and family management framework and implications for further development.
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