J Ernst1, K von Klitzing, E Brähler, G Romer, H Götze. 1. Department für Psychische Gesundheit, Abteilung für Medizinische Psychologie und Medizinische Soziologie, Universität Leipzig, Philipp-Rosenthal-Str. 55, 04103, Leipzig, Deutschland, Jochen.Ernst@medizin.uni-leipzig.de.
Abstract
BACKGROUND: There is increasing consideration of a family-focused perspective of the psychosocial consequences of cancer. OBJECTIVES: This study examined the psychosocial situation of children and adolescents (11 to 17 years old) of cancer patients assessing their psychological distress and coping over time. METHODS: A total of 110 children and adolescents were assessed post-treatment of parents with cancer (t1), 6 (t2) and 12 months (t3) after t1. Participants completed validated questionnaires assessing coping (KidCope) and depressive symptoms (CES). These data were compared with a matched sample from the general population. RESULTS: The children reported using a combination of coping measures. In particular, active coping was perceived as being helpful. In terms of coping, there were only small gender differences and 6 months after completion of treatment of the parents (t2), depressive symptoms of the children were still elevated. Depression diminished over time and was near the level of the comparison group at t3. CONCLUSION: Children and adolescents are particularly psychologically distressed after cancer treatment of parents. This distress was connected with not helpful coping strategies. The extended adjustment of children/adolescents of cancer patients has to be considered in the clinical and psychosocial care of the families.
BACKGROUND: There is increasing consideration of a family-focused perspective of the psychosocial consequences of cancer. OBJECTIVES: This study examined the psychosocial situation of children and adolescents (11 to 17 years old) of cancerpatients assessing their psychological distress and coping over time. METHODS: A total of 110 children and adolescents were assessed post-treatment of parents with cancer (t1), 6 (t2) and 12 months (t3) after t1. Participants completed validated questionnaires assessing coping (KidCope) and depressive symptoms (CES). These data were compared with a matched sample from the general population. RESULTS: The children reported using a combination of coping measures. In particular, active coping was perceived as being helpful. In terms of coping, there were only small gender differences and 6 months after completion of treatment of the parents (t2), depressive symptoms of the children were still elevated. Depression diminished over time and was near the level of the comparison group at t3. CONCLUSION:Children and adolescents are particularly psychologically distressed after cancer treatment of parents. This distress was connected with not helpful coping strategies. The extended adjustment of children/adolescents of cancerpatients has to be considered in the clinical and psychosocial care of the families.
Authors: Mikael Thastum; Maggie Watson; Christian Kienbacher; Jorma Piha; Barbara Steck; Robert Zachariae; Christiane Baldus; Georg Romer Journal: Cancer Date: 2009-09-01 Impact factor: 6.860
Authors: M Watson; I St James-Roberts; S Ashley; C Tilney; B Brougham; L Edwards; C Baldus; G Romer Journal: Br J Cancer Date: 2006-01-16 Impact factor: 7.640