The objective of the observational study is to examine the effect of MOVALIS (Meloxicam) therapy on Health Related Quality of Life (HRQoL) in the diverse region of Central and Eastern Europe. The Medical Outcomes Study 12 Item Short Form Health Survey version 2 (SF-12v2) will be used as the instrument to measure any change in physical wellbeing (Physical Component Summary, PCS) and mental wellbeing (Mental Component Summary, MCS) of patients following MOVALIS (Meloxicam) therapy.
Study Type
OBSERVATIONAL
Enrollment
3,569
Boehringer Ingelheim Investigational Site
Split, Croatia
Boehringer Ingelheim Investigational Site
Zagreb, Croatia
Boehringer Ingelheim Investigational Site
Aš, Czechia
Boehringer Ingelheim Investigational Site
Babice, Czechia
Boehringer Ingelheim Investigational Site
Benátky nad Jizerou, Czechia
Mean Change in Medical Outcomes Study 12-item Short-Form Health Survey, Version 2 Score From Baseline to Final Visit.
Physical Component Summary (PCS) Mean Difference final-baseline score. The Medical Outcomes Study 12-item Short-Form Health Survey, version 2 (SF-12v2) was used as the instrument to measure any changes in physical wellbeing (physical component summary, PCS) and mental wellbeing (mental component summary, MCS) in patients taking MOVALIS® therapy for approximately 4 weeks. Worst value 0 (lowest wellbeing), best value 100 (highest wellbeing)
Time frame: baseline and final visit (approximately 4 weeks)
Mean Change in SF 12 MCS Score From Baseline to Final Final Visit.Medical Outcomes Study 12-Item Short-Form Health Survey, Version 2
Mental Component Summary (MCS). Mean Difference final-baseline score. Worst value 0 (lowest wellbeing), best value 100 (highest wellbeing)
Time frame: Baseline and final visit (approximately 4 weeks)
Change From Baseline of Pain Intensity on Visual Analogue Scale
The effect of MOVALIS® on reduction of pain intensity was assessed by the change from baseline in patient assessment of pain intensity on a Visual Analogue Scale (VAS) ranging from 0 (no pain) to 100 (severe pain)
Time frame: Approximately four weeks of treatment
Patient Assessment of Efficacy
Patient assessment of general efficacy of MOVALIS® using a 5-point scale (1 excellent; 2 very good; 3 good; 4 fair; 5 poor) was performed at visit 2. The patients have been placed into categories according to the points on a scale.
Time frame: after approximately 4 weeks of treatment
Physician Assessment of Efficacy
Physician assessment of general efficacy of MOVALIS® using a 5-point scale (1 excellent; 2 very good; 3 good; 4 fair; 5 poor) was performed at visit 2. The patients have been placed into categories according to the points on a scale.
Time frame: after approximately 4 weeks of treatment
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Boehringer Ingelheim Investigational Site
Benesov Nad Ploucnicí, Czechia
Boehringer Ingelheim Investigational Site
Benesov U Prahy, Czechia
Boehringer Ingelheim Investigational Site
Benešov, Czechia
Boehringer Ingelheim Investigational Site
Beroun, Czechia
Boehringer Ingelheim Investigational Site
Bílina, Czechia
...and 309 more locations