The data of the IND-VFQ-33 were fitted to the Rasch model and the main validation indices were explored (
Table 3). The 33-item IND-VFQ scale had disordered thresholds in its first rating scale, suggesting that the clarity and/or number of response categories was suboptimal. Consequently, categories 2 and 3 (
a little and
quite a bit) were collapsed, resulting in four final response options for each rating scale. The capacity for the scale to function as an overall measure was then explored, although its psychometric properties were suboptimal (
Table 3). Consequently, the three subscales as proposed by the developers were separately assessed.
For the general functioning scale, the PSI and PR scores were 4.24 and 0.95, respectively, indicating that the scale was able to distinguish between four or more strata of vision-specific functioning. However, although the PCA for the first factor explained >60% of the variance, the unexplained variance in the first contrast of the residuals was 3.0, suggesting evidence of multidimensionality, and two items (items 5 and 9) demonstrated substantial misfit (MNSQ > 1.3). Analysis of the standardized residual loadings for items in the PCA revealed a set of items loading together (>0.4) pertaining to mobility. Thus, the overall general functioning scale was split into a mobility and an activity limitation scale (
Table 1). Both new scales demonstrated unidimensionality, the activity limitation scale only after removal of several misfitting items (eigenvalue first contrast 1.9 and variance by first factor > 60% for both scales;
Table 3), and good discriminant ability. However, although the mobility scale did not have any misfitting items, several others were identified in the activity limitation scale (5, 6, 9, 15, 16; infit MNSQ values > 1.3) and these were iteratively deleted until no misfitting items remained. The targeting of both the mobility and activity limitation scales was suboptimal (person mean, 2.94 and 1.93, respectively;
Table 3), but this is most likely due to the considerable proportion of patients with no or only mild visual impairment.
For the psychosocial impact and the visual symptoms scales, the PSI and PR scores were 2.00 and 0.80, and 2.24 and 0.83, respectively, indicating that these two scales were able to distinguish between three strata of patients' vision-specific functioning (
Table 3). Visual inspection of the person–item map for the psychosocial impact scale indicated suboptimal targeting because perceived participant ability was higher than the visual ability required to undertake the items. Therefore, persons with extreme scores at the high spectrum of ability level were deleted from the analysis, which improved the overall targeting; however, since this did not improve other fit statistics, these highly able participants were retained in the final analysis. Targeting of the symptoms scale was adequate. No misfitting items were detected for either the psychosocial or symptoms scales. Finally, there was no evidence of multidimensionality for the psychosocial and visual symptoms scales in this sample (
Table 3). No significant DIF for factors such as age, sex, and visual impairment was found for any item. Taken together, these fit parameters indicate that the four subscales of the IND-VFQ-33 are valid, reliable, and unidimensional and can be used to assess the impact of visual impairment on VRQoL.
The participants' mean ± SD scores for the IND-VFQ mobility, activity limitation, psychosocial impact, and visual symptoms subscales were, respectively, 51.92 ± 23.51, 61.88 ± 23.78, 60.82 ± 18.81, and 64.30 ± 17.79. Factors independently associated with VRQoL were therefore considered to be clinically meaningful if the CI limits of their beta coefficients were >12 or < −12, >12 or < −12, >9.5 or < −9.5, and >9 or < −9 for the mobility, activity limitation, psychosocial impact, and visual symptoms subscales, respectively, which is approximately half the SD of the overall mean.