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Main Outcome Measures: Shoulder subluxation (radiograph), shoulder pain (Brief Pain Inventory), motor impairment (Fugl-Meyer score), shoulder pain-free external rotation (handheld goniometer), and disability (FIM™ instrument) were assessed before treatment (T1), after 6 weeks of neuromuscular stimulation (T2), and at 3-month follow-up (T3).
The internal consistency and confirmatory factor analysis of the instrument were assessed.
The validity, reliability, and reproducibility of this instrument were assessed in a previous study [ 19].
Psychometric properties of the final instrument were assessed in a sample of 261 nursing students.
The convergent validity and discriminant validity of the instrument were assessed by the multitrait-multimethod matrix.
Convergent, discriminant and construct validity of the instrument were assessed by classical test theory (CTT).
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First, internal consistency of the instrument was assessed using Cronbach's coefficient alpha reliability.
Upon completion of this set of interviews, the instrument was assessed for translatability and finalized for quantitative testing.
Table 1 People involved in the Translatability Assessment (TA) process People to be involved Qualifications Rationale Developer(s) of the patient-reported outcome (PRO) measure Researcher(s) involved in the development of the instrument being assessed.
Prior to any analysis of the item responses collected in this campus-wide student sample, the psychometric quality (domain sampling) of the information yielded by the instrument was assessed.
The difference in mean scores between PGC morale groups for each instrument was assessed using one-way ANOVA.
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