Content validity testing of the INTERMED Self‐Assessment in a sample of adults with rheumatoid arthritis and rheumatology healthcare providers

Author:

Dhiman Kiran1ORCID,Hall Marc2ORCID,Crump Trafford34ORCID,Hoens Alison M.567ORCID,Lacaille Diane58ORCID,Rankin James A.2ORCID,Then Karen L.2ORCID,Hazlewood Glen1359ORCID,Barnabe Cheryl1359ORCID,Katz Steven10ORCID,Sutherland Jason11,Dempsey Erika1,Barber Claire E. H.1359ORCID

Affiliation:

1. Department of Medicine, Cumming School of Medicine University of Calgary Calgary Alberta Canada

2. Faculty of Nursing University of Calgary Calgary Alberta Canada

3. Department of Community Health Sciences, Cumming School of Medicine University of Calgary Calgary Alberta Canada

4. Department of Surgery, Cumming School of Medicine University of Calgary Calgary Alberta Canada

5. Arthritis Research Canada Vancouver British Columbia Canada

6. Department of Physical Therapy University of British Columbia Vancouver British Columbia Canada

7. Arthritis Patient Advisory Board, Arthritis Research Canada Vancouver British Columbia Canada

8. Department of Medicine University of British Columbia Vancouver British Columbia Canada

9. McCaig Institute for Bone and Joint Health Calgary Alberta Canada

10. Department of Medicine University of Alberta Edmonton Alberta Canada

11. Centre for Health Services and Policy Research University of British Columbia Vancouver British Columbia Canada

Abstract

AbstractBackgroundCare complexity can occur when patients experience health challenges simultaneously with social barriers including food and/or housing insecurity, lack of transportation or other factors that impact care and patient outcomes. People with rheumatoid arthritis (RA) may experience care complexity due to the chronicity of their condition and other biopsychosocial factors. There are few standardised instruments that measure care complexity and none that measure care complexity specifically in people with RA.ObjectivesWe assessed the content validity of the INTERMEDS Self‐Assessment (IMSA) instrument that measures care complexity with a sample of adults with RA and rheumatology healthcare providers (HCPs). Cognitive debriefing interviews utilising a reparative framework were conducted.MethodsPatient participants were recruited through two existing studies where participants agreed to be contacted about future studies. Study information was also shared through email blasts, posters and brochures at rheumatology clinic sites and trusted arthritis websites. Various rheumatology HCPs were recruited through email blasts, and divisional emails and announcements. Interviews were conducted with nine patients living with RA and five rheumatology HCPs.ResultsThree main reparative themes were identified: (1) Lack of item clarity and standardisation including problems with item phrasing, inconsistency of the items and/or answer sets and noninclusive language; (2) item barrelling, where items asked about more than one issue, but only allowed a single answer choice; and (3) timeframes presented in the item or answer choices were either too long or too short, and did not fit the lived experiences of patients. Items predicting future healthcare needs were difficult to answer due to the episodic and fluctuating nature of RA.ConclusionsDespite international use of the IMSA to measure care complexity, patients with RA and rheumatology HCPs in our setting perceived that it did not have content validity for use in RA and that revision for use in this population under a reparative framework was unfeasible. Future instrument development requires an iterative cognitive debriefing and repair process with the population of interest in the early stages to ensure content validity and comprehension.Patient or Public ContributionPatient and public contributions included both patient partners on the study team and people with RA who participated in the study. Patient partners were involved in study design, analysis and interpretation of the findings and manuscript preparation. Data analysis was structured according to emergent themes of the data that were grounded in patient perspectives and experiences.

Funder

Canadian Institutes of Health Research

Publisher

Wiley

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