Literature DB >> 17498080

Psychological aspects and coping styles of parents with Haemophilic child undergoing a programme of counselling and psychological support.

A M Bottos1, E Zanon, M T Sartori, A Girolami.   

Abstract

Parents of children affected by haemophilia must face, often without prior knowledge, the difficult challenge imposed by such a pathology. To satisfy the need of information, guideline and psychological support for a better quality of life, 30 parents with haemophiliac children have participated in a programme of counselling and psychological support. Such a programme has the aim of guiding the group trough a process of discovery, comparison and personal growth and stimulating adaptive processes of problem-solving and decision-making. The aim of this paper was to verify how the programme influenced coping strategies and other psychological constructs such as depression and anxiety. Subjects of this study were administered the following psychological tests: COPE (coping, orientation to problems experienced), BDI (beck depression inventory), STAI-Y form (state-trait anxiety inventory) at the beginning and at the end of the programme. The results show that by the end of the programme subjects are characterized by a greater use of problem-focused coping strategies, typical of individuals who think that the situation is susceptible to change, and a minor use of emotion-focused coping strategies, related to individuals who regard the situation as immutable. The use of avoidance -focused coping strategies seems to remain at the same level even if it was low. Also the other psychological aspects investigated, namely depression and anxiety, did receive a positive influence. The results show how significant such programme has been for parents.

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Mesh:

Year:  2007        PMID: 17498080     DOI: 10.1111/j.1365-2516.2006.01428.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  6 in total

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Journal:  Pediatr Nephrol       Date:  2010-05-12       Impact factor: 3.714

2.  Quality of Life, Perception of Disease and Coping Strategies in Patients with Hemophilia in Spain and El Salvador: A Comparative Study.

Authors:  Rubén Cuesta-Barriuso; Ana Torres-Ortuño; Joaquín Nieto-Munuera; José Antonio López-Pina
Journal:  Patient Prefer Adherence       Date:  2021-08-21       Impact factor: 2.711

3.  Assessment of mother and father concern in childhood hydrocephalus.

Authors:  Abhaya V Kulkarni
Journal:  Qual Life Res       Date:  2007-09-09       Impact factor: 4.147

Review 4.  Hemophilia Care in the Pediatric Age.

Authors:  Marta Bertamino; Francesca Riccardi; Laura Banov; Johanna Svahn; Angelo Claudio Molinari
Journal:  J Clin Med       Date:  2017-05-19       Impact factor: 4.241

5.  Psychological interventions for people with hemophilia.

Authors:  Laura Palareti; Giannino Melotti; Frederica Cassis; Sarah J Nevitt; Alfonso Iorio
Journal:  Cochrane Database Syst Rev       Date:  2020-03-18

6.  Social support and resilience in persons with severe haemophilia: An interpretative phenomenological analysis.

Authors:  Kateřina Ratajová; Jan Blatný; Iva Poláčková Šolcová; Zdeněk Meier; Tekla Horňáková; Robert Brnka; Peter Tavel
Journal:  Haemophilia       Date:  2020-04-14       Impact factor: 4.287

  6 in total

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