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Understanding motivation for Australian adolescents and young adults with cystic fibrosis

Modifiable factors to support self‐management

Bibliographic Data

ID12288686
AuthorsLucy Holland (0000-0003-1917-1478, Faculty of Health and Medicine The University of Newcastle Newcastle New South Wales Australia, corresponding author), Jodi Hilton (0000-0001-8337-1728, Department of Respiratory and Sleep Medicine John Hunter Children’s Hospital Newcastle New South Wales Australia), Kim Cookson (Department of Respiratory and Sleep Medicine John Hunter Hospital Newcastle New South Wales Australia), Milena Heinsch (0000-0002-8014-9475, School of Medicine and Public Health & Behavioural Sciences The University of Newcastle Newcastle New South Wales Australia), Conor Gilligan (0000-0001-5493-4309, School of Medicine and Public Health & Behavioural Sciences The University of Newcastle Newcastle New South Wales Australia), Peter AB Wark (0000-0001-5676-6126, John Hunter Hospital), Peter Wark (Centre for Healthy Lungs Hunter Medical Research Institute The University of Newcastle Newcastle New South Wales Australia)
Year2022
Volume30
Issue5
Pagese2712-e2723
Publication date2022-01-08
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueHealth & Social Care in the Community (JOURNAL)
Journal identifiersISSN: 0966-0410 • E-ISSN: 1365-2524
PublisherWiley (PUBLISHER • GB)
DOI10.1111/hsc.13714
PMID34997788
OpenAlexW4206632995
LanguageEN
References cited44

Cystic fibrosis (CF) is Australia's most common life limiting genetic condition, characterised by declining health and quality of life (QoL) over time. Despite improvements in treatment, there remains no cure. Adolescents and young adults (AYAs) with CF experience broad impacts to psychosocial functioning and QoL, as well as major transitions in care, all at a time of significant developmental change. The importance of developmentally tailored approaches to youth health care and self-management for young people with CF are well understood. However, to date, models of youth specific self-management have been lacking and motivation for young people with CF has not been well explored. This qualitative study, based on a social constructionist epistemological framework, addresses this gap. A total of 21 AYAs aged 15-30 years were recruited through one paediatric and one adult Australian CF centre. Demographic, clinical and distress data were captured to describe health complexity. Semi-structured interviews were audio-recorded, transcribed and analysed using thematic analysis. Participants were representative of Australian AYAs with CF by demography and clinical status. Alarmingly, over a third reported clinically significant distress. Two themes emerged. The first Identified impacts to motivation and self-management resulting from the challenges of managing CF, life and care. These included time and competing priorities, changing health statis, mental health, social factors, unmet needs and health system complexity. The second identified factors that support motivation including: achievement, meaning and purpose; consequence avoidance; and accountability. These results illustrate the importance of AYA specific, theoretically founded, holistic self-management models which extend beyond current theoretical approaches that aim to understand behaviour change or address barriers, in isolation from motivation. Improved approaches to care based on these findings are essential to foster positive behavioural change, support self-management and foster the best health outcomes for young people living with CF

Developmental psychology · Distress · Mental health · Psychiatry · Psychosocial · Qualitative research · Quality of life (healthcare · Self-management · Thematic analysis · Adolescent and Pediatric Healthcare · Clinical Psychology · Cystic Fibrosis Research Advances · Family and Disability Support Research · Medicine · Nursing · Psychology

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