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Text
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URL Address
<a href="http://doi.org/10.1093/jpepsy/jsm011" target="_blank" rel="noreferrer">http://doi.org/10.1093/jpepsy/jsm011</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
A name given to the resource
Brief report: psychosocial functioning of fathers as primary caregivers of pediatric oncology patients
Publisher
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Journal of Pediatric Psychology
Date
A point or period of time associated with an event in the lifecycle of the resource
2007
Subject
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Child; Humans; Male; Adult; Questionnaires; Social Adjustment; Psychology; Stress; Social Behavior; Psychological/diagnosis/epidemiology/psychology; Caregivers/statistics & numerical data; Disabled Children/statistics & numerical data; father experience; Fathers/psychology/statistics & numerical data; Neoplasms/epidemiology
Creator
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Bonner MJ; Hardy KK; Willard VW; Hutchinson KC
Description
An account of the resource
OBJECTIVE: To evaluate the psychosocial functioning of fathers as primary caregivers of pediatric oncology patients. METHODS: Fathers who identified themselves as the primary medical caregivers were given a packet of questionnaires, including the Brief Symptom Inventory (BSI), the Impact of Event Scale (IES), the Impact on Family Scale (IFS), the Caregiver Strain Questionnaire (CGSQ), and the Parent Experience of Child Illness (PECI) scale, to complete and return by mail. The 23 fathers who returned the questionnaire packets were compared with 23 mothers who were matched on demographic variables. RESULTS: There were no differences between groups on self-report measures of distress or illness-related parenting stress. Descriptively, however, the majority of parents were above normative means on measures of psychological distress with a significantly greater proportion of fathers endorsing elevated levels of depression on the BSI. CONCLUSION: Including fathers in pediatric psychosocial research is important and represents a growing trend in psycho-oncology.
2007
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1093/jpepsy/jsm011" target="_blank" rel="noreferrer">10.1093/jpepsy/jsm011</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2007
Adult
Backlog
Bonner MJ
Caregivers/statistics & numerical data
Child
Disabled Children/statistics & numerical data
father experience
Fathers/psychology/statistics & numerical data
Hardy KK
Humans
Hutchinson KC
Journal Article
Journal of Pediatric Psychology
Male
Neoplasms/epidemiology
Psychological/diagnosis/epidemiology/psychology
Psychology
Questionnaires
Social Adjustment
Social Behavior
Stress
Willard VW
-
Text
A resource consisting primarily of words for reading. Examples include books, letters, dissertations, poems, newspapers, articles, archives of mailing lists. Note that facsimiles or images of texts are still of the genre Text.
Citation List Month
Backlog
URL Address
<a href="http://doi.org/10.1093/jpepsy/jsj034" target="_blank" rel="noreferrer">http://doi.org/10.1093/jpepsy/jsj034</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Development and validation of the parent experience of child illness
Publisher
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Journal of Pediatric Psychology
Date
A point or period of time associated with an event in the lifecycle of the resource
2005
Subject
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Family; Parents; PedPal Lit; Caregiver; Child Illness
Creator
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Bonner MJ; Hardy KK; Guill AB; McLaughlin C; Schweitzer H; Carter K
Description
An account of the resource
Objective To develop a measure of parent adjustment related to caring for a child with achronic illness and to evaluate the reliability and validity of the measure with a group of parentsof children with brain tumors. Methods One-hundred forty-nine parents of patients(age <1–17 years) diagnosed with a brain tumor were assessed using the 25-item self-reportParent Experience of Child Illness (PECI). Internal consistency, construct validity, and factorstructure were assessed. Results Exploratory factor analysis yielded four theoreticallycoherent factors including: Guilt and Worry, Emotional Resources, Unresolved Sorrowand Anger, and Long-term Uncertainty. Internal reliability for the PECI scales ranged from.72 to .89, suggesting acceptable reliability. As evidence of construct validity, the PECI scalesshow significant, positive correlations with scales from established measures of parentadjustment. Conclusion The PECI augments the current literature by providing a briefmeasure of parents’ subjective distress and perceived Emotional Resources, domains that arecritical but understudied in children with chronic illness and their caregivers.
2005
Identifier
An unambiguous reference to the resource within a given context
<a href="http://doi.org/10.1093/jpepsy/jsj034" target="_blank" rel="noreferrer">10.1093/jpepsy/jsj034</a>
Rights
Information about rights held in and over the resource
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
The nature or genre of the resource
Journal Article
2005
Backlog
Bonner MJ
Caregiver
Carter K
Child Illness
Family
Guill AB
Hardy KK
Journal Article
Journal of Pediatric Psychology
McLaughlin C
Parents
PedPal Lit
Schweitzer H