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Overall, all the scales chosen are based on previous studies, although the wording of some of the measures was changed to adapt to the informal learning context.
In two trials one of the initially registered outcome measures was changed to a secondary outcome measure (NCT00204750) and (NCT00606619).
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The primary outcome measure was changed in average daily pain diary score (baseline versus final week).
The 'policy compliant' measure was retained but the duration measure was changed from duration <24hr to single dose prophylaxis.
New testing of psychometric properties is warranted when a non-standardized measure is changed for subsequent use and is essentially altered into a different measure [ 25].
Additional outcome measures were changes in PPT, 5-HT platelet poor plasma (P-5-HT), as well as pain distribution.
Primary outcome measures were changes in the JFK Coma Recovery Scale-Revised (CRS-R) scale total score and Clinical Global Impression Improvement (CGI-I) scale.
Primary outcome measures were change in monthly migraine days and 50% responder rate, i.e. the percentage of subjects having a ≥ 50% reduction of monthly migraine days.
Primary outcome: The primary outcome measures were change in HbA1c, peal VO2, and biochemical analyses in T2D patients after a 12-week concurrent ET program.
Primary outcome measures were changes in body composition, and metabolic abnormalities, secondary outcome measures were virologic and immunologic efficacy and overall safety.
The main outcome measures were change in HbA1c and body weight, and final insulin dose.
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CEO of Professional Science Editing for Scientists @ prosciediting.com