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. Author manuscript; available in PMC: 2020 May 18.
Published in final edited form as: Eur J Cancer Care (Engl). 2016 Jan 18;26(3):10.1111/ecc.12437. doi: 10.1111/ecc.12437

Table 1 –

Latent Class Solutions and Fit Indices for the Time 1 and Time 2 Assessments Using Symptom Occurrence Ratingsa

Time 1 Assessment – Prior to Next Dose of Chemotherapy
Model LL AIC BIC VLMR Entropy
2 Class −13465.34 27032.68 27277.55 2375.10**** .84
3 Classb −13217.76 26589.51 26959.21 495.17**** .83
4 Class −13084.89 26375.78 26870.31 265.73ns .80
Time 2 Assessment – Following the Next Dose of Chemotherapy
2 Class −13286.83 26675.67 26920.53 2320.59**** .83
3 Classb −13021.47 26196.94 26566.64 530.73**** .81
4 Class −12892.35 25990.71 26485.24 258.23ns .79
ns

Not significant

*

p < .05

**

p < .01

***

p < .001

****

p < .0001

a

In order to have a sufficient number of patients with each symptom to perform the latent class analyses, the MSAS symptoms that occurred in at least 40% of the patients were identified. This criterion was selected to provide assurance that sufficient information was available to identify classes that were not sample-specific, due to infrequent reports of symptoms. A total of 25 out of 32 symptoms from the MSAS occurred in >40% of the patients.

b

The 3-class solution was selected because the VLMR was significant for the 3-class solution, indicating that three classes fit the data better than two classes, and the VLMR was not significant for the 4-class solution, indicating that too many classes had been extracted.

Note. LL = log-likelihood; AIC = Akaike Information Criterion, BIC = Bayesian Information Criterion; VLMR = Vuong-Lo-Mendell-Rubin likelihood ratio test for the K vs. K-1 model.