Study Design. A longitudinal study using patient questionnaires was perform
ed.
Objective. To compare the discriminatory power and responsiveness of the Ab
erdeen Back Pain Scale (ABPS), the Poland Disability Questionnaire (RDQ), a
nd the EuroQol in patients with low back pain.
Summary of Background Data. A number instruments specific to low back pain
have not been compared for measurement properties. The EuroOol is a widely
used generic instrument that has not been compared with specific instrument
s in patients with back pain.
Methods. A questionnaire incorporating the Aberdeen Back Pain Scale, the Po
land Disability Questionnaire, and the EuroOol was completed by patients ta
king part in a clinical trial of exercise treatments for back pain. Patient
s completed follow-up questionnaires at 6 weeks, 6 months, and 1 year. The
discriminatory power of these instruments was assessed against variables re
lating to activity limitations, medication, and comorbidity. Responsiveness
was assessed using standardized response means.
Results. The questionnaire was completed by 187 patients taking part in the
clinical trial. The Aberdeen instrument was found to be the most powerful
at discriminating between different groups of patients on variables relatin
g to activity limitations, medication, and comorbidity. The specific instru
ments demonstrated good levels of responsiveness, with the Aberdeen instrum
ent producing the largest standardized response means. The Aberdeen instrum
ent was more responsive to the smaller changes experienced by the control g
roup, but was less powerful than the Roland at measuring differences in the
levels of change between the two groups of patients at two of the three fo
llow-up assessments in the trial. The EuroOol demonstrated a moderate level
of responsiveness.
Conclusions. The two specific instruments are capable of greater levels of
discrimination between groups of patients, and are more responsive over tim
e than the generic EuroOol. The Aberdeen instrument performed most satisfac
torily in relation to these criteria, but the Roland instrument was more se
nsitive to differences between the two groups in the clinical trial. The me
asurement properties of these two instruments reflect their origin: The Abe
rdeen instrument is based on clinical questions, whereas the Poland instrum
ent is based on the generic Sickness Impact Profile. Instrument content sho
uld be carefully considered when selecting instruments for applications, in
cluding clinical trials.