"I sort of never felt like I should be worried about it or that I could be worried about it'" an interpretative phenomenological analysis of perceived barriers to disclosure by young people with coeliac disease

被引:8
作者
Wheeler, Miranda [1 ]
David, Annabel L. [2 ]
Kennedy, Juliet [2 ]
Knight, Matthew [1 ]
机构
[1] Univ Oxford, Oxford Hlth NHS Fdn Trust, Oxford Ctr Psychol Hlth, Oxford Inst Clin Psychol Training & Res, Oxford, England
[2] Oxford Univ Hosp NHS Fdn Trust, Oxford Childrens Hosp, Childrens Psychol Med, Oxford, England
关键词
coeliac disease; disclosure; interpretative phenomenological analysis; paediatrics; psychological difficulties; stigma; GLUTEN-FREE; DIABETES SERVICES; HEALTH; ADOLESCENTS; ADULTS; EXPERIENCES; TRANSITION; ADHERENCE; RESPONSES; CHILDREN;
D O I
10.1111/bjhp.12599
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objectives There has been little research in the United Kingdom regarding young people's experiences of disclosure of psychological difficulties relating to coeliac disease (CD) to others, particularly healthcare professionals. This study sought to address this systematically with a focus on the lived experiences of young people with CD. This study aimed to gain insight into how paediatric gastroenterology services could improve the patient experience for those with CD and support the identification of patients who may benefit from further psychological support. Design This study used interpretive phenomenological analysis (IPA) of patient accounts. Methods Seven young people with CD (aged 11-16 years) were recruited from a UK hospital paediatric gastroenterology service. Semi-structured interviews were carried out and verbatim transcripts were analysed using IPA to explore young people's experiences of CD and why they might feel able or unable to disclose psychological difficulties associated with their condition to clinicians. Results Three superordinate themes were interpreted from the data. The first encapsulated experiences of adjusting to the diagnosis within a developmental context, including the role of adults in information provision and the importance of peer support. The second outlined experiences of managing perceived or actual stigma regarding others' perceptions of the condition and themselves. The third incorporated perceived barriers to disclosure relating to power, safety, and beliefs about the role of medical professionals. Conclusions Findings highlight the importance of clinicians continually providing developmentally appropriate information to young people and actively breaking down barriers to disclosure through body language and the use of clear questions regarding emotional experiences.
引用
收藏
页码:1296 / 1313
页数:18
相关论文
共 46 条
[11]   "You don't need a prescription to go gluten-free": The scientific self-diagnosis of celiac disease [J].
Copelton, Denise A. ;
Valle, Giuseppina .
SOCIAL SCIENCE & MEDICINE, 2009, 69 (04) :623-631
[12]   Healthcare experiences and quality of life of adults with coeliac disease: a cross-sectional study [J].
Crocker, H. ;
Jenkinson, C. ;
Peters, M. .
JOURNAL OF HUMAN NUTRITION AND DIETETICS, 2020, 33 (06) :741-751
[13]   How do children and adolescents experience healthcare professionals? Scoping review and interpretive synthesis [J].
Davison, Gail ;
Kelly, Martina Ann ;
Conn, Richard ;
Thompson, Andrew ;
Dornan, Tim .
BMJ OPEN, 2021, 11 (07)
[14]   Young adults' (16-25 years) suggestions for providing developmentally appropriate diabetes services: a qualitative study [J].
Dovey-Pearce, G ;
Hurrell, R ;
May, C ;
Walker, C ;
Doherty, Y .
HEALTH & SOCIAL CARE IN THE COMMUNITY, 2005, 13 (05) :409-419
[15]   Psychosocial aspects of coeliac disease: A cross-sectional survey of a UK population [J].
Ford, Sarah ;
Howard, Ruth ;
Oyebode, Jan .
BRITISH JOURNAL OF HEALTH PSYCHOLOGY, 2012, 17 :743-757
[16]   Celiac disease [J].
Green, PHR ;
Jabri, B .
ANNUAL REVIEW OF MEDICINE, 2006, 57 :207-221
[17]   Coeliac disease [J].
Green, PHR ;
Jabri, B .
LANCET, 2003, 362 (9381) :383-391
[18]  
Guandalini S., 2014, CELIAC DIS, P177
[19]   Perceived barriers and facilitators to mental health help-seeking in young people: a systematic review [J].
Gulliver, Amelia ;
Griffiths, Kathleen M. ;
Christensen, Helen .
BMC PSYCHIATRY, 2010, 10
[20]   The Child Illness and Resilience Program (CHiRP): a study protocol of a stepped care intervention to improve the resilience and wellbeing of families living with childhood chronic illness [J].
Katrina M Hamall ;
Todd R Heard ;
Kerry J Inder ;
Katherine M McGill ;
Frances Kay-Lambkin .
BMC Psychology, 2 (1)