106 results on '"Frances Marcus Lewis"'
Search Results
102. Family Coping Strategies and Chronic Illness in the Mother
- Author
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Kathleen M. Stetz, Frances Marcus Lewis, and Janet Primomo
- Subjects
Coping (psychology) ,Longitudinal study ,Content area ,medicine.disease ,Mutually exclusive events ,Education ,Breast cancer ,Content analysis ,Developmental and Educational Psychology ,medicine ,Family coping ,Statistical analysis ,Psychology ,Social Sciences (miscellaneous) ,Clinical psychology - Abstract
The purpose of the current study was to describe the types of coping strategies household families use to manage problems that affect them when the mother has a chronic illness. Data presented are cross-sectional data from first occasion interviews collected as part of a larger longitudinal study of 125 families (Lewis, Woods, & Ellison, 1983) in which the mother has either breast cancer, fibrocystic breast disease or diabetes. The instrument used to collect data on family coping was the Problem Centered Family Coping Interview (Lewis, 1983). Study families reported a mean number of 4.02 coping strategies per family. Using content analysis, 55 mutually exclusive coping strategies were identified from open-ended interview questions. These 55 categories were combined into 10 composite categories by content area for purposes of statistical analysis. The most frequent composite category reported by the study sample was alterations in household management which represented 38% of the types of strategies employed by these families. The type of chronic illness in the mother did not differentiate the families by categories of management strategies.
- Published
- 1986
- Full Text
- View/download PDF
103. Clinical tool development for adult chemotherapy patients
- Author
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Frances Marcus Lewis, Sue Parsell, and Sharon Cannell Firsich
- Subjects
Chemotherapy ,medicine.medical_specialty ,Oncology ,Oncology (nursing) ,Process (engineering) ,business.industry ,medicine.medical_treatment ,Medicine ,business ,Intensive care medicine - Published
- 1979
- Full Text
- View/download PDF
104. Experienced Personal Control and Quality of Life in Late-Stage Cancer Patients
- Author
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Frances Marcus Lewis
- Subjects
Locus of control ,Quality of life ,medicine ,Anxiety ,Psychological testing ,Context (language use) ,Learned helplessness ,medicine.symptom ,Psychology ,General Nursing ,Internal-External Control ,Test (assessment) ,Clinical psychology - Abstract
This study examined the association of experienced personal control and quality of life for late-stage cancer patients within the context of Rotter's Social Learning Theory and Seligman's Theory of Learned Helplessness. It was hypothesized that in late-stage cancer patients greater control would be associated with a higher quality of life as measured by self-esteem, anxiety, and perceived self-esteem, anxiety, and perceived meaningfulness. The longer the history of the disease, the lower would be the individual's level of experienced personal control and quality of life. Fifty-seven late-stage cancer patients completed four standardized instruments: the Rosenberg Self-Esteem Scale; the Health Locus of Control Scale (HLC); the Lewis, Firsich, and Parsell Attorney Scale; and the Crumbaugh Purpose-in-Life Test. As predicted, the measure of experienced personal control over life significantly correlated with scores on the self-esteem scale (tau = -.33; p = .001), and the anxiety scale (tau = -.30; p = .001). Contrary to prediction, scores on the Health Locus of Control Scale were only significantly associated with scores on the Purpose-In-Life Test (tau = -.18; p = .05). Length of history of disease was significantly related to scores on the HLC Scale (tau = .27; p = .007) and to scores on the anxiety scale (tau = .20; p = .03) but was not significantly associated with scores on the self-esteem scale or the Purpose-In-Life Test.
- Published
- 1982
- Full Text
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105. Environmental Enrichment After Primary Glioma Radiation Therapy.
- Author
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Figuracion KCF, Mac Donald CL, Hunt D, McGranahan TM, Lewis FM, Rockhill J, Goldberg M, Halasz L, and Thompson HJ
- Subjects
- Humans, Male, Female, Middle Aged, Cross-Sectional Studies, Adult, Aged, Quality of Life psychology, Glioma radiotherapy, Glioma psychology, Brain Neoplasms radiotherapy, Brain Neoplasms psychology
- Abstract
Objectives: To explore and describe the health outcomes and levels of environmental enrichment (EE) in participants with brain tumors after radiation therapy (RT)., Sample & Setting: 39 participants with glioma (grades 2-3) treated with RT were recruited within five years of original diagnosis from a neuro-oncology clinic., Methods & Variables: A cross-sectional design was employed. EE measures included social connectedness, physical activity, employment, and financial stability. Health outcome measures included the Montreal Cognitive Assessment, Symbol Digit Modalities Test, global cortical atrophy rate scale, Karnofsky Performance Status Scale, and MD Anderson Symptom Inventory-Brain Tumor Module. Descriptive statistics characterized the health outcomes between participants who received photon RT and proton beam RT., Results: Participants who received photon RT with high EE showed higher scores on the Montreal Cognitive Assessment, Symbol Digit Modalities Test, and Karnofsky Performance Status Scale, and lower scores on the global cortical atrophy rate scale and MD Anderson Symptom Inventory-Brain Tumor Module., Implications for Nursing: EE may reduce symptom burden, promote healthy brain aging, and improve cognitive and functional status in glioma survivors receiving photon RT.
- Published
- 2024
- Full Text
- View/download PDF
106. Family history of cardiovascular disease, perceived cardiovascular disease risk, and health-related behavior: a review of the literature.
- Author
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Imes CC and Lewis FM
- Subjects
- Cardiovascular Diseases prevention & control, Health Knowledge, Attitudes, Practice, Health Promotion, Humans, Life Style, Primary Prevention, Risk Assessment, Sex Factors, Cardiovascular Diseases genetics, Health Behavior, Risk Reduction Behavior
- Abstract
Background: More than 82 million Americans have 1 or more forms of cardiovascular disease (CVD), accounting for 32.8% of all deaths in the United States. Although the evidence for the familial aggregation of CVD is strong, the relationship between family history (FH) of CVD, perceived risk for CVD, and health-related behavior is poorly understood., Objective: The objective of this article was to review and summarize the published research on the relationship between an FH of CVD, an individual's perceived risk, and health-related behavior to make recommendations for clinical practice and future research., Methods: A literature search was conducted using PubMed, CINAHL Plus, and PsycINFO to identify articles that examined the relationship between an FH of CVD, perceived CVD risk, and health-promoting behaviors. A total of 263 unique articles were reviewed. A total of 238 were excluded, resulting in a total of 25 articles included in the review., Results: There was a positive relationship between a reported FH of CVD and perceived risk. However, the relationship between an FH of CVD and health-related behavior change and perceived risk and behavior change was inconsistent., Conclusions: A person's awareness of his or her FH of CVD or his or her own risk for CVD is not a sufficient predictor of changes in his or her health-related behavior. Future studies are needed to better explain the processes by which perceived CVD risk or FH of CVD can be used to affect health-related behavior changes. It appears that both FH and perceived personal risk for CVD are necessary but not sufficient conditions to change health-related behavior in high-risk populations. Future studies should also test interventions that help individuals with an FH of CVD attribute increased personal risk to themselves for developing CVD, while providing lifestyle management options to minimize their risk.
- Published
- 2014
- Full Text
- View/download PDF
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