01.12.2015 | Research article | Ausgabe 1/2015 Open Access

Psychometric properties of a new treatment expectation scale in rheumatoid arthritis: an application of item response theory
- Zeitschrift:
- BMC Musculoskeletal Disorders > Ausgabe 1/2015
Electronic supplementary material
Competing interests
Authors’ contributions
Background
Methods
A. The Physical domain (physical impact of RA): with the new treatment, I expect:
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Q1: The swelling of the joints to be
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Much better
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Better
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Same
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Worse
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Much Worse
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non-applicable
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Q2: The pain to be
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Much better
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Better
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Same
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Worse
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Much Worse
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non-applicable
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Q3: My morning stiffness to be
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Much better
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Better
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Same
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Worse
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Much Worse
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non-applicable
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Q4: My mobility to be
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Much better
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Better
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Same
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Worse
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Much Worse
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non-applicable
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Q5: My fatigue to be
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Much better
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Better
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Same
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Worse
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Much Worse
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non-applicable
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Q6: The visible signs of RA (e.g. deformities on my hands) to be
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Much better
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Better
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Same
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Worse
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Much Worse
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non-applicable
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Q7: The joint damage to be caused by RA
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Much better
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Better
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Same
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Worse
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Much Worse
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non-applicable
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Questions for physical domain are coded from 5 = Much better to 0 = non-applicable; overall score for the physical domain ranges between 0 and 35.
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B. The Psycho-social domain (emotional wellbeing and social aspects of RA): with the new treatment, I expect:
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Q1: To be able to maintain my independence (e.g. not needing to ask for help making tea)
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Much more than usual
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More than usual
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Same
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Worse than usual
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Much worse than usual
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non-applicable
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Q2: Improvements in my general health in order for me to be able to go back to work and/ or stay in salaried employment: (Please tick here if not applicable)
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Much more than usual
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More than usual
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Same
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Worse than usual
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Much worse than usual
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non-applicable
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Q3: My everyday activities (e.g. shopping) to be facilitated:
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Much more than usual
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More than usual
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Same
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Worse than usual
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Much worse than usual
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non-applicable
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Q4: To feel in control of my RA self manage (e.g. diet)/ cope (e.g. frustration) alongside medical treatment
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Much more than usual
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More than usual
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Same
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Worse than usual
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Much worse than usual
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non-applicable
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Q5: To be able to maintain my social roles (e.g. supporting family/going out with friends)
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Much more than usual
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More than usual
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Same
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Worse than usual
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Much worse than usual
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non-applicable
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Q6: My emotional wellbeing (e.g. mood) to be
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Much more than usual
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More than usual
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Same
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Worse than usual
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Much worse than usual
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non-applicable
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Questions for the Psycho-social domain are coded from 5 = Much more than usual to 0 = non-applicable; overall score for the psycho-social domain range between 0 and 30.
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C. Impact of new Treatment (Overall Expectations on Impact of Treatment (care delivery)): with the new treatment I expect it:
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Q1: To make me feel better overall despite side effects
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Q2: To reduce the likelihood of surgery
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Q3: To prevent other physical complications
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Q4: To come with detailed information from the medical staff:
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Q5: To allow me to be involved in the treatment decision making with the clinical staff
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Q6: To include regular physical (e.g. hands and feet) assessments
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Q7: To include regular emotional wellbeing assessments
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Q8: To allow me to not have to change medication so often
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Strongly Agree
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Agree
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Neither Agree nor Disagree
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Disagree
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Strongly Disagree
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non-applicable
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Questions for the impact of new treatment are coded from 5 = strongly agree to 0 = non-applicable; overall score for the impact of new treatment scores range between 0 and 40.
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Data analysis
n = 138
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n (%)
|
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Mean age (SD)
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54 (14.30)
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Gender
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Female
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101 (73 %)
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Male
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37 (27 %)
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Ethnicity
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White
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73 (53 %)
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Other
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65 (47 %)
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Disability
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Yes
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48 (35 %)
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No/Unsure
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90 (65 %)
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Results
Study participants
MAPLe-RA scale properties
Item discriminations
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Item difficulties
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---|---|---|---|---|
Items
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Estimate (SE)
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P-value
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Estimate (SE)
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P-value
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Physical domain
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||||
Swelling of the joints
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1.38 (0.58)
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0.018
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−1.22 (0.30)
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<0.001
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Pain
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1.74 (0.82)
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0.034
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−1.25 (0.30)
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<0.001
|
Morning stiffness
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1.25 (0.47)
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0.008
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−1.00 (0.25)
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<0.001
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Mobility
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1.04 (0.41)
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0.012
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−1.16 (0.31)
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<0.001
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Fatigue
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0.87 (0.26)
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0.001
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−0.96 (0.25)
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<0.001
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Visible signs of RA
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0.49 (0.16)
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0.002
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0.19 (0.24)
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0.427
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Joint damage
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0.40 (0.15)
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0.006
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−0.62 (0.34)
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0.066
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Psycho-social domain
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||||
Maintain my independence
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1.46 (0.39)
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<0.001
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−0.14 (0.13)
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0.270
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Improvements in my general health
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0.85 (0.23)
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<0.001
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0.06 (0.17)
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0.712
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Everyday activities
|
1.27 (0.40)
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0.001
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−0.32 (0.14)
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0.027
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To feel in control of my RA self-manage
|
1.64 (0.49)
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0.001
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−0.46 (0.13)
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0.001
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To maintain my social roles
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1.87 (0.63)
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0.003
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−0.30 (0.12)
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0.016
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My emotional well-being
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1.77 (0.51)
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0.001
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−0.42 (0.13)
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0.001
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Impact of new Treatment
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||||
Feel better overall
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1.47 (0.38)
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<0.001
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−1.02 (0.20)
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<0.001
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Reduce the likelihood of surgery
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0.89 (0.27)
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0.001
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−1.19 (0.29)
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<0.001
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To prevent other physical complications
|
0.70 (0.27)
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0.008
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−1.47 (0.44)
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0.001
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To come with detailed information from the
medical staff
|
1.16 (0.45)
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0.010
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−1.36 (0.34)
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<0.001
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Decision making with the clinical staff
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0.87 (0.34)
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0.010
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−1.65 (0.47)
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<0.001
|
Regular physical assessment
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1.41 (0.52)
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0.007
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−1.36 (0.29)
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<0.001
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Regular emotional well-being
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0.81 (0.26)
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0.001
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−0.90 (0.25)
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<0.001
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Not to have to change medication
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0.52 (0.18)
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0.005
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−1.14 (0.40)
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0.004
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