Literature DB >> 12621241

Psychosocial needs of families with a child with cancer.

Gustaf Ljungman1, Patrick J McGrath, Elisabeth Cooper, Kimberley Widger, Jill Ceccolini, Conrad V Fernandez, Gerri Frager, Krista Wilkins.   

Abstract

PURPOSE: The aims of this study were to map the problems and needs of children with cancer and their families with regard to possible psychosocial interventions, and to do an acceptability study of different ways to provide support.
METHODS: The authors performed a cross-sectional structured telephone interview with 56 parents of children with cancer and 13 adolescents from these families. On 0 to 10 analog scales, parents and adolescents rated the importance of different needs, how these needs had been met, the acceptability of different ways of providing supportive interventions, how often these ways had been used, and comfort using them.
RESULTS: Parents' mean rating of importance of information needs was 9.42, peer social support 7.84, and self-management therapy 9.21. The ratings of how well these needs had been met were 8.05, 5.30, and 7.13, respectively. Both parents and adolescents ranked getting information written on paper highest, preferred to communicate in a face-to-face support group for peer social support, and preferred a therapist for self-management therapy. The comfort ratings for using different ways to provide the interventions were all high, as was access; 89% of families had computers in their homes, 76% had Internet access.
CONCLUSIONS: The needs for information, peer social support, and self-management therapy are all high. There is still room to meet these needs better. Using paper-based, telephone, computer CD, or an interactive Web-based intervention package all seem to be acceptable and accessible ways to meet the needs and might reduce the risk of families developing psychosocial problems.

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Year:  2003        PMID: 12621241     DOI: 10.1097/00043426-200303000-00008

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  7 in total

1.  Development and evaluation of an educational interactive CD-ROM for teens with cancer.

Authors:  Judith K Jones; Sharmila A Kamani; Patricia J Bush; Karen A Hennessy; Aditya Marfatia; Aziza T Shad
Journal:  Pediatr Blood Cancer       Date:  2010-09       Impact factor: 3.167

2.  Palliative care for children and adolescents in Switzerland: a needs analysis across three diagnostic groups.

Authors:  Susanne Inglin; Rainer Hornung; Eva Bergstraesser
Journal:  Eur J Pediatr       Date:  2011-01-29       Impact factor: 3.183

Review 3.  The adolescent with a chronic condition. Part II: healthcare provision.

Authors:  P-A Michaud; J-C Suris; R Viner
Journal:  Arch Dis Child       Date:  2004-10       Impact factor: 3.791

4.  The relationship between lung cancer patients' educational level and evaluation of their treatment information needs.

Authors:  Joy M Jacobs-Lawson; Mitzi M Schumacher; Travonia Hughes; Susanne Arnold
Journal:  J Cancer Educ       Date:  2009       Impact factor: 2.037

Review 5.  Informational Support in Pediatric Oncology: Review of the Challenges Among Arab Families.

Authors:  Naïma Otmani; Mohammed Khattab
Journal:  J Cancer Educ       Date:  2018-08       Impact factor: 2.037

6.  Pain Management and Use of Opioids in Pediatric Oncology in India: A Qualitative Approach.

Authors:  Paola Angelini; Katherine M Boydell; Vicky Breakey; Purna A Kurkure; Marian A Muckaden; Eric Bouffet; Brijesh Arora
Journal:  J Glob Oncol       Date:  2016-11-02

7.  Young patients', parents', and survivors' communication preferences in paediatric oncology: results of online focus groups.

Authors:  Marieke Zwaanswijk; Kiek Tates; Sandra van Dulmen; Peter M Hoogerbrugge; Willem A Kamps; Jozien M Bensing
Journal:  BMC Pediatr       Date:  2007-11-09       Impact factor: 2.125

  7 in total

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