Mixed-methods study identifying key intervention targets to improve participation in daily living activities in primary Sjögren's syndrome patients

Hackett, Kate, Deane, Katherine, Newton, Julia, Deary, Vincent, Bowman, Simon, Rapley, Tim and Ng, Wan-Fai (2018) Mixed-methods study identifying key intervention targets to improve participation in daily living activities in primary Sjögren's syndrome patients. Arthritis Care & Research, 70 (7). pp. 1064-1073. ISSN 2151-464X

[img]
Preview
Text
Hackett_et_al-2018-Arthritis_Care.pdf - Published Version
Available under License Creative Commons Attribution 4.0.

Download (393kB) | Preview
[img] Text
acr23536.pdf - Accepted Version
Restricted to Repository staff only until 6 February 2019.

Download (475kB) | Request a copy
Official URL: https://doi.org/10.1002/acr.23536

Abstract

Objective - Functional ability and participation in life situations are compromised in many primary Sjögren's syndrome (PSS) patients. This study aims to identify the key barriers and priorities to participation in daily living activities, in order to develop potential future interventions.

Methods - Group concept mapping (GCM), a semi-quantitative, mixed-methods, approach was used to identify and structure ideas from UK PSS patients, adults living with a PSS patient (AHMs) and health care professionals (HCPs). Brainstorming generated ideas, which were summarised into a final set of statements. Participants individually arranged these statements into themes and rated each statement for importance. Multidimensional scaling and hierarchical cluster analysis were applied to sorted and rated data to produce visual representations of the ideas (concept maps), enabling identification of agreed priority areas for interventions.

Results - 121 patients, 43 AHMs and 67 HCPs took part. 463 ideas were distilled down to 94 statements. These statements were grouped into seven clusters; ‘Patient empowerment’, ‘Symptoms’, ‘Wellbeing’, ‘Access and coordination of healthcare’, ‘Knowledge and support’, ‘Public awareness and support’ and ‘Family and friends’. Patient empowerment and Symptoms were rated as priority conceptual themes. Important statements within priority clusters indicate patients should be taken seriously and supported to self-manage symptoms of oral and ocular dryness, fatigue, pain and poor sleep.

Conclusion - Our data highlighted that in addition to managing PSS symptoms; interventions aiming to improve patient empowerment, general wellbeing, access to healthcare, patient education and social support are important to facilitate improved participation in daily living activities.

Item Type: Article
Subjects: L500 Social Work
Department: Faculties > Health and Life Sciences > Social Work, Education and Community Wellbeing
Depositing User: Becky Skoyles
Date Deposited: 13 Feb 2018 09:43
Last Modified: 18 Jul 2018 10:45
URI: http://nrl.northumbria.ac.uk/id/eprint/33340

Actions (login required)

View Item View Item

Downloads

Downloads per month over past year

View more statistics


Policies: NRL Policies | NRL University Deposit Policy | NRL Deposit Licence