Literature DB >> 24889289

The development and initial validation of a questionnaire to measure help-seeking behaviour in patients with new onset rheumatoid arthritis.

Rebecca J Stack1,2, Christian D Mallen3, Chris Deighton4, Patrick Kiely5, Karen L Shaw6, Alison Booth4, Kanta Kumar1,2, Susan Thomas2, Ian Rowan2, Rob Horne7, Peter Nightingale8, Sandy Herron-Marx9, Clare Jinks3, Karim Raza1,2.   

Abstract

BACKGROUND: Early treatment for rheumatoid arthritis (RA) is vital. However, people often delay in seeking help at symptom onset. An assessment of the reasons behind patient delay is necessary to develop interventions to promote rapid consultation.
OBJECTIVE: Using a mixed methods design, we aimed to develop and test a questionnaire to assess the barriers to help seeking at RA onset.
DESIGN: Questionnaire items were extracted from previous qualitative studies. Fifteen people with a lived experience of arthritis participated in focus groups to enhance the questionnaire's face validity. The questionnaire was also reviewed by groups of multidisciplinary health-care professionals. A test-retest survey of 41 patients with newly presenting RA or unclassified arthritis assessed the questionnaire items' intraclass correlations.
RESULTS: During focus groups, participants rephrased questions, added questions and deleted items not relevant to the questionnaire's aims. Participants organized items into themes: early symptom experience, initial reactions to symptoms, self-management behaviours, causal beliefs, involvement of significant others, pre-diagnosis knowledge about RA, direct barriers to seeking help and relationship with GP. The test-retest survey identified seven items (out of 79) with low intraclass correlations which were removed from the final questionnaire.
CONCLUSION: The involvement of people with a lived experience of arthritis and multidisciplinary health-care professionals in the preliminary validation of the DELAY (delays in evaluating arthritis early) questionnaire has enriched its development. Preliminary assessment established its reliability. The DELAY questionnaire provides a tool for researchers to evaluate individual, cultural and health service barriers to help-seeking behaviour at RA onset.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  delay in accessing health services; face validity; patient involvement; questionnaire development; rheumatoid arthritis; test-retest reliability

Mesh:

Year:  2014        PMID: 24889289      PMCID: PMC5810627          DOI: 10.1111/hex.12203

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  32 in total

Review 1.  Mapping the impact of patient and public involvement on health and social care research: a systematic review.

Authors:  Jo Brett; Sophie Staniszewska; Carole Mockford; Sandra Herron-Marx; John Hughes; Colin Tysall; Rashida Suleman
Journal:  Health Expect       Date:  2012-07-19       Impact factor: 3.377

2.  Illness representations: a prototype approach.

Authors:  G D Bishop; S A Converse
Journal:  Health Psychol       Date:  1986       Impact factor: 4.267

3.  The influence of ethnicity on the extent of, and reasons underlying, delay in general practitioner consultation in patients with RA.

Authors:  Kanta Kumar; Enid Daley; Fazal Khattak; Christopher D Buckley; Karim Raza
Journal:  Rheumatology (Oxford)       Date:  2010-02-26       Impact factor: 7.580

4.  Patient perspective of measuring treatment efficacy: the rheumatoid arthritis patient priorities for pharmacologic interventions outcomes.

Authors:  T Sanderson; M Morris; M Calnan; P Richards; S Hewlett
Journal:  Arthritis Care Res (Hoboken)       Date:  2010-05       Impact factor: 4.794

5.  Progress since OMERACT 6 on including patient perspective in rheumatoid arthritis outcome assessment.

Authors:  John R Kirwan; Monica Ahlmén; Maarten de Wit; Turid Heiberg; Maggie Hehir; Sarah Hewlett; Patricia P Katz; Patricia Minnock; Enid M Quest; Pam Richards
Journal:  J Rheumatol       Date:  2005-11       Impact factor: 4.666

6.  Patient perspective: reasons and methods for measuring fatigue in rheumatoid arthritis.

Authors:  John R Kirwan; Sarah Hewlett
Journal:  J Rheumatol       Date:  2007-05       Impact factor: 4.666

7.  Patient perspective: fatigue as a recommended patient centered outcome measure in rheumatoid arthritis.

Authors:  John R Kirwan; Patricia Minnock; Ade Adebajo; Barry Bresnihan; Ernest Choy; Maarten de Wit; Mieke Hazes; Pam Richards; Kenneth Saag; Maria Suarez-Almazor; George Wells; Sarah Hewlett
Journal:  J Rheumatol       Date:  2007-05       Impact factor: 4.666

8.  Benefit of very early referral and very early therapy with disease-modifying anti-rheumatic drugs in patients with early rheumatoid arthritis.

Authors:  V P K Nell; K P Machold; G Eberl; T A Stamm; M Uffmann; J S Smolen
Journal:  Rheumatology (Oxford)       Date:  2004-04-27       Impact factor: 7.580

9.  Reasons for medical help-seeking behaviour of patients with recent-onset arthralgia.

Authors:  Jessica A B van Nies; Elisabeth Brouwer; Diederik P C de Rooy; Floris A van Gaalen; Tom W J Huizinga; Marcel D Posthumus; Annette H M van der Helm-van Mil
Journal:  Ann Rheum Dis       Date:  2012-09-06       Impact factor: 19.103

10.  EULAR recommendations for terminology and research in individuals at risk of rheumatoid arthritis: report from the Study Group for Risk Factors for Rheumatoid Arthritis.

Authors:  Danielle M Gerlag; Karim Raza; Lisa G M van Baarsen; Elisabeth Brouwer; Christopher D Buckley; Gerd R Burmester; Cem Gabay; Anca I Catrina; Andrew P Cope; François Cornelis; Solbritt Rantapää Dahlqvist; Paul Emery; Stephen Eyre; Axel Finckh; Steffen Gay; Johanna M Hazes; Annette van der Helm-van Mil; Tom W J Huizinga; Lars Klareskog; Tore K Kvien; Cathryn Lewis; Klaus P Machold; Johan Rönnelid; Dirkjan van Schaardenburg; Georg Schett; Josef S Smolen; Sue Thomas; Jane Worthington; Paul P Tak
Journal:  Ann Rheum Dis       Date:  2012-03-02       Impact factor: 19.103

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  4 in total

1.  Patient and researcher perspectives on facilitating patient and public involvement in rheumatology research.

Authors:  Judith Pollock; Karim Raza; Arthur G Pratt; Helen Hanson; Stefan Siebert; Andrew Filer; John D Isaacs; Christopher D Buckley; Iain B McInnes; Marie Falahee
Journal:  Musculoskeletal Care       Date:  2016-12-16

2.  Delays between the onset of symptoms and first rheumatology consultation in patients with rheumatoid arthritis in the UK: an observational study.

Authors:  Rebecca Jayne Stack; Peter Nightingale; Clare Jinks; Karen Shaw; Sandy Herron-Marx; Rob Horne; Chris Deighton; Patrick Kiely; Christian Mallen; Karim Raza
Journal:  BMJ Open       Date:  2019-03-04       Impact factor: 2.692

3.  Determinants of continued maternal care seeking during pregnancy, birth and postnatal and associated neonatal survival outcomes in Kenya and Uganda: analysis of cross-sectional, demographic and health surveys data.

Authors:  Malachi Ochieng Arunda; Anette Agardh; Benedict Oppong Asamoah
Journal:  BMJ Open       Date:  2021-12-13       Impact factor: 2.692

4.  Development and formative evaluation of patient research partner involvement in a multi-disciplinary European translational research project.

Authors:  Rebecca Birch; Gwenda Simons; Heidi Wähämaa; Catherine M McGrath; Eva C Johansson; Diana Skingle; Kerin Bayliss; Bella Starling; Danielle M Gerlag; Christopher D Buckley; Rebecca J Stack; Karim Raza; Marie Falahee
Journal:  Res Involv Engagem       Date:  2020-02-19
  4 in total

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