Using confirmatory factor analysis to evaluate construct validity of the Brief Pain Inventory (BPI).
Using confirmatory factor analysis to evaluate construct validity of the Brief Pain Inventory (BPI).
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使用验证性因素分析评估短暂疼痛清单(BPI)的构造有效性。
DOI:
10.1016/j.jpainsymman.2010.05.008
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发表时间:
2011-03
影响因子:
4.7
通讯作者:
Basch, Ethan
中科院分区:
文献类型:
--
作者:
Atkinson, Thomas M.;Rosenfeld, Barry D.;Sit, Laura;Mendoza, Tito R.;Fruscione, Mike;Lavene, Dawn;Shaw, Mary;Li, Yuelin;Hay, Jennifer;Cleeland, Charles S.;Scher, Howard I.;Breitbart, William S.;Basch, Ethan
The Brief Pain Inventory (BPI) is a frequently used instrument designed to assess the patient-reported outcome of pain. The majority of factor analytic studies have found a two-factor (i.e., pain intensity and pain interference) structure for this instrument; however, since the BPI was developed with an a priori hypothesis of the relationship among its items, it follows that construct validity investigations should utilize confirmatory factor analysis (CFA). The purpose of this work is to establish the construct validity of the BPI using a CFA framework and demonstrate factorial invariance using a range of demographic variables. A retrospective CFA was completed in a sample of individuals diagnosed with HIV/AIDS and cancer (n = 364; 63% male; age 21-92 years, M = 51.80). A baseline one-factor model was compared against two-factor and three-factor models (i.e., pain intensity, activity interference, and affective interference) that were developed based on the hypothetical design of the instrument. Fit indices for the three-factor model were statistically superior when compared to the one-factor model and marginally better in comparison to the two-factor model. This three-factor structure was found to be invariant across disease, age, and ethnicity groups. The results of this study provide evidence to support a three-factor representation of the BPI, as well as the originally hypothesized two-factor structure. Such findings will begin to provide clinical trialists, pharmaceutical sponsors, and regulators with confidence in the psychometric properties of this instrument when considering its inclusion in clinical research.
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DOI:
10.1080/10705519909540118
发表时间:
1999-01-01
影响因子:
6
作者:
Hu, Li-tze;Bentler, Peter M.
通讯作者:
Bentler, Peter M.
影响因子:
3.8
作者:
Olden M;Rosenfeld B;Pessin H;Breitbart W
通讯作者:
Breitbart W
影响因子:
2.1
作者:
Schreiber, James B.;Nora, Amaury;King, Jamie
通讯作者:
King, Jamie
影响因子:
10.3
作者:
Boelen, Paul A.;van den Hout, Marcel A.;van den Bout, Jan
通讯作者:
van den Bout, Jan
影响因子:
7.4
作者:
Cleeland, CS;Nakamura, Y;Serlin, RC
通讯作者:
Serlin, RC